WO2017041704A1 - Récepteur de lymphocyte t ayant une affinité élevée de ciblage de polypeptide à chaîne courte d'antigène rhamm - Google Patents

Récepteur de lymphocyte t ayant une affinité élevée de ciblage de polypeptide à chaîne courte d'antigène rhamm Download PDF

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WO2017041704A1
WO2017041704A1 PCT/CN2016/098248 CN2016098248W WO2017041704A1 WO 2017041704 A1 WO2017041704 A1 WO 2017041704A1 CN 2016098248 W CN2016098248 W CN 2016098248W WO 2017041704 A1 WO2017041704 A1 WO 2017041704A1
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tcr
amino acid
variable domain
chain variable
seq
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PCT/CN2016/098248
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Chinese (zh)
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李懿
黄仪有
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广州市香雪制药股份有限公司
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Priority to CN201680001312.1A priority Critical patent/CN106459178B/zh
Publication of WO2017041704A1 publication Critical patent/WO2017041704A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/46—Cellular immunotherapy
    • A61K39/464—Cellular immunotherapy characterised by the antigen targeted or presented
    • A61K39/4643—Vertebrate antigens
    • A61K39/4644—Cancer antigens
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503—Immunoglobulin superfamily
    • C07K14/7051—T-cell receptor (TcR)-CD3 complex
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/177—Receptors; Cell surface antigens; Cell surface determinants
    • A61K38/1774—Immunoglobulin superfamily (e.g. CD2, CD4, CD8, ICAM molecules, B7 molecules, Fc-receptors, MHC-molecules)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/46—Cellular immunotherapy
    • A61K39/461—Cellular immunotherapy characterised by the cell type used
    • A61K39/4611—T-cells, e.g. tumor infiltrating lymphocytes [TIL], lymphokine-activated killer cells [LAK] or regulatory T cells [Treg]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/46—Cellular immunotherapy
    • A61K39/463—Cellular immunotherapy characterised by recombinant expression
    • A61K39/4632—T-cell receptors [TCR]; antibody T-cell receptor constructs
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/70—Vectors or expression systems specially adapted for E. coli

Definitions

  • the present invention relates to the field of biotechnology, and more particularly to a T cell receptor (TCR) capable of recognizing a polypeptide derived from a RHAMM antigen.
  • TCR T cell receptor
  • the invention also relates to the preparation and use of said receptors.
  • TCR T cell receptor
  • TCR is the only receptor for a specific antigenic peptide presented on the major histocompatibility complex (MHC), which may be the only sign of abnormalities in the cell.
  • MHC major histocompatibility complex
  • APC antigen presenting cells
  • MHC class I and class II molecular ligands corresponding to TCR are also proteins of the immunoglobulin superfamily but are specific for antigen presentation, and different individuals have different MHCs, thereby presenting different shortness of one protein antigen Peptides to the surface of the respective APC cells.
  • Human MHC is commonly referred to as the HLA gene or the HLA complex.
  • RHAMM is an endogenous antigen that is degraded into small molecule polypeptides after intracellular production and binds to MHC (main histocompatibility complex) molecules to form a complex that is presented to the cell surface.
  • ILSLELMKL 165-173 is a short peptide derived from RHAMM (Greiner J, et al., Blood 2005, 106(3): 938-945).
  • RHAMM is expressed in a variety of tumor tissues, with leukemia (Greiner J, et al., Experimental hematology 2002, 30 (9): 1029-1035), colon cancer (Yamada Y, et al., Japanese journal Of cancer research: Gann 1999, 90(9): 987-992), breast cancer (Wang C, et al., Clinical cancer research: an official journal of the American Association for Cancer Research 1998, 4(3): 567- 576) is more prominent in other cancers such as gastric cancer (Li H, et al., International journal of oncology 2000, 17(5): 927-932), renal cancer (Greiner J, et al., Experimental hematology 2002, 30(9): 1029-1035), oral squamous cell carcinoma (Yamano Y, et al., International journal of oncology 2008, 32(5): 1001-1009), head and neck squamous cell carcinoma (Schmitt A, Et al., International journal of oncology
  • the ILSLELMKL-HLA A0201 complex provides a marker for TCR targeting tumor cells.
  • the TCR capable of binding to the ILSLELMKL-HLA A0201 complex has high application value for the treatment of tumors.
  • a TCR capable of targeting the tumor cell marker can be used
  • the cytotoxic agent or immunostimulatory agent is delivered to the target cell or transformed into T cells such that the TCR expressing the TCR is capable of destroying the tumor cells for administration to the patient during a treatment known as adoptive immunotherapy.
  • the ideal TCR has a higher affinity, allowing the TCR to reside on the targeted cells for a long period of time.
  • it is preferred to use a medium affinity TCR. Accordingly, those skilled in the art are directed to developing TCRs that target tumor cell markers that can be used to meet different purposes.
  • TCR T cell receptor
  • the T cell receptor has the property of binding to the ILSLELMKL-HLA A0201 complex.
  • the TCR comprises an alpha chain variable domain and a beta chain variable domain
  • the TCR alpha chain variable domain comprises three CDR regions
  • the reference sequences of the three CDR regions of the TCR alpha chain variable domain are as follows ,
  • CDR3 ⁇ AATNSGYALN and contains at least one of the following mutations:
  • the TCR ⁇ chain variable domain comprises three CDR regions, and the reference sequences of the three CDR regions of the TCR ⁇ chain variable domain are as follows.
  • CDR3 ⁇ AWSVDGAEQY and contains at least one of the following mutations:
  • the number of mutations in the CDR region of the TCR alpha chain variable domain is 3 or 4 or 6 or 7 or 8 or 9 or 11.
  • the number of mutations in the CDR region of the TCR ⁇ chain variable domain is 2 or 3 or 5 or 6 or 7 or 8 or 9.
  • the TCR comprises a TCR alpha chain variable domain and a TCR beta chain variable domain, wherein the TCR beta chain variable domain comprises CDR1 ⁇ , CDR2 ⁇ , and CDR3 ⁇ , wherein
  • the CDR3 ⁇ comprises the sequence: DGAEQY and is 10 amino acid residues in length.
  • the DGAEQY is located at positions 5-10 of the CDR3 ⁇ .
  • the CDR3 ⁇ comprises the sequence: [3 ⁇ X1][3 ⁇ X2]S[3 ⁇ X3]DGAEQY, wherein [3 ⁇ X1], [3 ⁇ X2], [3 ⁇ X3] are independently selected from any natural amino acid residue.
  • the [3 ⁇ X1] is A or S.
  • the [3 ⁇ X2] is W or Y.
  • the [3 ⁇ X3] is V or L.
  • the CDR3 ⁇ comprises a sequence selected from the group consisting of:
  • the CDR2[beta] comprises the sequence: SVG.
  • the CDR2 ⁇ comprises the sequence: SVG[2 ⁇ X1][2 ⁇ X2], wherein [2 ⁇ X1], [2 ⁇ X2] are independently selected from any natural amino acid residue.
  • the [2 ⁇ X1] is I or V.
  • the [2 ⁇ X2] is G or R.
  • the CDR2 ⁇ comprises a sequence selected from the group consisting of:
  • the CDR1 ⁇ comprises a sequence selected from the group consisting of:
  • PHSPRL preferably
  • LDDLRI preferably
  • LRYIRA preferably
  • LSNTRA preferably
  • GTSNPN preferably
  • the TCR alpha chain variable domain comprises CDR1 ⁇ , CDR2 ⁇ , and CDR3 ⁇ .
  • the CDR3 ⁇ comprises the sequence: AATN, and the CDR3 ⁇ is 8-13 amino acids in length, preferably 10 amino acids.
  • the CDR3 ⁇ comprises the sequence: AATN[3 ⁇ X1]G[3 ⁇ X2]S[3 ⁇ X3][3 ⁇ X4]N, wherein [3 ⁇ X1], [3 ⁇ X2], [3 ⁇ X3] are independently selected from any natural Amino acid residues.
  • the [3 ⁇ X1] is S or D.
  • the [3 ⁇ X2] is Y or I.
  • the [3 ⁇ X3] is A, I, H or V.
  • the CDR3 ⁇ comprises a sequence selected from the group consisting of:
  • AATNDGIIIN (preferably), AATNDGILIN (preferably), AATNDGYHMN (preferably), AATNDGYVMN (preferably), AATNSGYALN AATNDGIHIN, and AATNDGIIFN.
  • the CDR2 ⁇ comprises the sequence: [2 ⁇ X1]Y[2 ⁇ X2][2 ⁇ X3]G[2 ⁇ X4], wherein [2 ⁇ X1], [2 ⁇ X2], [2 ⁇ X3], [2 ⁇ X4] are independently selected from any Natural amino acid residues.
  • the [2 ⁇ X1] is I or L.
  • the [2 ⁇ X2] is S or R.
  • the [2 ⁇ X3] is N or G.
  • the [2 ⁇ X4] is D, S or T.
  • the CDR2 ⁇ comprises a sequence selected from the group consisting of:
  • IYRNGT preferably
  • LYRGGS preferably
  • IYSNGD IYRNGT
  • the CDR1 ⁇ comprises the sequence: D[1 ⁇ X1][1 ⁇ X2][1 ⁇ X3]Q[1 ⁇ X4], wherein [1 ⁇ X1], [1 ⁇ X2], [1 ⁇ X3], [1 ⁇ X4] are independently selected from any Natural amino acid residues.
  • the [1 ⁇ X1] is I, M, K, or R.
  • the [1 ⁇ X2] is Y, L or V.
  • the [1 ⁇ X3] is N, or S.
  • the [1 ⁇ X4] is S or A.
  • the CDR1 ⁇ comprises a sequence selected from the group consisting of:
  • DIYNQS (best), DIYNQA (preferably), DKLNQS, DMLNQS (preferably), and DRVSQS.
  • the TCR alpha chain variable domains of the TCRs do not simultaneously comprise the following CDRs:
  • CDR1 ⁇ DRVSQS
  • CDR2 ⁇ IYSNGD
  • CDR3 ⁇ AATNSGYALN.
  • the TCR ⁇ chain variable domains of the TCRs do not simultaneously comprise the following CDRs:
  • CDR1 ⁇ GTSNPN
  • CDR2 ⁇ SVGIG
  • CDR3 ⁇ AWSVDGAEQY.
  • the TCR has a CDR selected from the group consisting of:
  • the TCR is mutated in the alpha chain variable domain set forth in SEQ ID NO: 36, and the mutated amino acid residue sites include 28R, 29V, 30S, 32S, 50I, 52S, One or more of 53N, 55D, 94S, 96Y, 97A or 98L, wherein the amino acid residue numbering is the number shown in SEQ ID NO: 36;
  • the TCR is mutated in the ⁇ -chain variable domain of SEQ ID NO: 37, and the mutated amino acid residue sites include 27G, 28T, 29S, 30N, 31P, 32N, One or more of 53I, 54G, 92A, 93W or 95V, wherein the amino acid residue numbering is the number shown in SEQ ID NO:37.
  • the mutated TCR alpha chain variable domain of the present invention comprises one or more amino acid residues selected from the group consisting of: 28I, 28K, or 28M; 29Y or 29L; 30N; 32A; 50L; 52R; 53G; 55S or 55T; 94D; 96I; 97H, 97I, 97V or 97L; 98M, 98I or 98F; wherein the amino acid residue numbering uses the number shown in SEQ ID NO: 36;
  • the mutated TCR ⁇ chain variable domain of the present invention comprises one or more amino acid residues selected from the group consisting of: 27P or 27L; 28H, 28S, 28R or 28D; 29N, 29Y or 29D 30P, 30T, 30I or 30L; 31R; 32L, 32A or 32I; 53V; 54R; 92S; 93Y; 95L; wherein the amino acid residue numbering is the number shown in SEQ ID NO:37.
  • the TCR is an alpha beta heterodimeric TCR
  • the alpha chain variable domain of the TCR comprises at least 90% (preferably, at least 92%) of the amino acid sequence set forth in SEQ ID NO:36 More preferably, at least 94%; most preferably, at least 96%) of the amino acid sequence of sequence homology.
  • the TCR is an ⁇ heterodimeric TCR
  • the ⁇ chain variable domain of the TCR comprises at least 90% (preferably, at least 92%) of the amino acid sequence set forth in SEQ ID NO:37 More preferably, at least 94%; most preferably, at least 97%) of the amino acid sequence of sequence homology.
  • the TCR comprises (i) all or part of its transmembrane domain a TCR alpha chain, and (ii) all or part of a TCR beta chain except for its transmembrane domain, wherein both (i) and (ii) comprise a variable domain of the TCR chain and at least a portion of the constant domain.
  • amino acid sequence of the alpha chain variable domain of the TCR is selected from the group consisting of: SEQ ID NO: 40-56;
  • the beta strand variable domain amino acid sequence of the TCR is selected from the group consisting of: SEQ ID NOs: 57-69.
  • the TCR is an ⁇ heterodimeric TCR, and an artificial interchain disulfide bond is contained between the ⁇ chain variable region of the TCR and the ⁇ chain constant region.
  • a cysteine residue forming an artificial interchain disulfide bond between the alpha chain variable region of the TCR and the beta chain constant region is substituted for one or more groups selected from the group consisting of point:
  • the TCR comprising an artificial interchain disulfide bond between the alpha chain variable region and the beta chain constant region comprises an alpha chain variable domain and a beta chain variable domain and all but the transmembrane domain or Part of the beta strand constant domain, but it does not comprise an alpha chain constant domain, the alpha chain variable domain of the TCR forming a heterodimer with the beta strand.
  • the TCR is an alpha beta heterodimeric TCR comprising (i) all or part of a TCR alpha chain other than its transmembrane domain, and (ii) all but its transmembrane domain Or a partial TCR ⁇ chain, wherein both (i) and (ii) comprise a variable domain of the TCR chain and at least a portion of the constant domain, and an artificial interchain disulfide bond is contained between the alpha chain constant region and the beta chain constant region.
  • a cysteine residue forming an artificial interchain disulfide bond between the TCR ⁇ and the constant region of the ⁇ chain replaces one or more sets of sites selected from the group consisting of:
  • the TCR is a single chain TCR.
  • the TCR is a single-chain TCR consisting of an alpha chain variable domain and a beta chain variable domain, the alpha chain variable domain and the beta chain variable domain consisting of a flexible short peptide sequence (linker) )connection.
  • the hydrophobic core of the TCR is mutated.
  • the alpha chain variable domain of the TCR comprises at least 90% (preferably, at least 92%; more preferably, at least 94%; most preferred) of the amino acid sequence set forth in SEQ ID NO:3 , at least 96%; for example, an amino acid sequence which may be at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence homology) homology;
  • the ⁇ chain variable domain of the TCR comprises at least 90% (preferably, at least 92%; more preferably, at least 94%; most preferably) of the amino acid sequence set forth in SEQ ID NO:4. , at least 97%; for example, may be at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence homology) amino acid sequence homology.
  • the hydrophobic core mutation of the TCR occurs at one or more amino acid residue positions selected from the group consisting of: 19A, 21L, and 79S, wherein the alpha chain variable domain of SEQ ID NO: 36 is selected from the group consisting of: The amino acid residue numbering is given by the number shown in SEQ ID NO:36.
  • the hydrophobic core mutation of the TCR occurs at one or more amino acid residue positions selected from the group consisting of the ⁇ chain variable domain set forth in SEQ ID NO: 37: 13Q, 19L, 64L, 78S And 81L, wherein the amino acid residue numbering is the number shown in SEQ ID NO:37.
  • the alpha chain variable domain of the TCR after the hydrophobic core mutation comprises one or more amino acid residues selected from the group consisting of 19V, 21I and 79I; wherein the amino acid residue numbering is SEQ ID NO: the number shown in 36;
  • the ⁇ -chain variable domain of the TCR after the hydrophobic core mutation comprises one or more amino acid residues selected from the group consisting of 13V, 19V, 64Y, 78I and 81V; wherein, amino acid residues The numbering uses the number shown in SEQ ID NO:37.
  • amino acid sequence of the alpha chain variable domain of the TCR is selected from the group consisting of: SEQ ID NOs: 6-22;
  • the beta strand variable domain amino acid sequence of the TCR is selected from the group consisting of: SEQ ID NOs: 23-35.
  • the TCR is soluble.
  • the binding affinity of the TCR to the ILSLELMKL-HLA A0201 complex is at least 2 times the binding affinity of the wild type TCR to the ILSLELMKL-HLA A0201 complex; preferably at least 5 fold; more preferably , at least 10 times.
  • the binding affinity of the TCR to the ILSLELMKL-HLA A0201 complex is at least 100 times the binding affinity of the wild type TCR to the ILSLELMKL-HLA A0201 complex; preferably at least 10 3 fold; Preferably, at least 10 4 fold; most preferably, the binding affinity of the TCR of the invention to the ILSLELMKL-HLA A0201 complex is 10 5 -10 6 times the binding affinity of the wild-type TCR to the ILSLELMKL-HLA A0201 complex.
  • the solution of the TCR ILSLELMKL-HLA A0201 complex dissociation equilibrium constant K D ⁇ 100 ⁇ M Preferably, 10 ⁇ M ⁇ K D ⁇ 100 ⁇ M; more preferably, 1 ⁇ M ⁇ K D ⁇ 10 ⁇ M.
  • the dissociation equilibrium constant K D of the TCR to the ILSLELMKL-HLA A0201 complex is ⁇ 1 ⁇ M; preferably, 10 nM ⁇ K D ⁇ 1 ⁇ M; more preferably, 100 pM ⁇ K D ⁇ 10 nM.
  • the C- or N-terminus of the alpha chain and/or beta strand of the TCR incorporates a conjugate.
  • the conjugate that binds to the TCR is a detectable label, a therapeutic agent, a PK modified moiety, or a combination of any of these.
  • the therapeutic agent that binds to the TCR is an anti-CD3 antibody linked to the C- or N-terminus of the alpha or beta chain of the TCR.
  • the amino acid sequence of the ⁇ chain variable domain of the TCR that binds to the anti-CD3 antibody is selected from the group consisting of: SEQ ID NO: 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 and 56; and/or the ⁇ chain variable domain amino acid sequence of the TCR bound to the anti-CD3 antibody is selected from the group consisting of: SEQ ID NO: 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69.
  • amino acid sequence of the high affinity TCR and anti-CD3 antibody fusion molecule of the invention is preferably selected from the group consisting of: SEQ ID NOs: 70-82.
  • a multivalent TCR complex comprising at least two TCR molecules, and wherein at least one TCR molecule is the TCR of the first aspect of the invention.
  • a nucleic acid molecule comprising a nucleic acid sequence encoding the TCR molecule of the first aspect of the invention or the multivalent TCR complex of the second aspect of the invention, or a complement thereof, is provided sequence;
  • a vector comprising the nucleic acid molecule of the third aspect of the invention is provided.
  • a host cell comprising the vector of the fourth aspect of the invention or the nucleic acid molecule of the third aspect of the invention integrated with exogenous in the chromosome is provided.
  • an isolated cell expressing the TCR of the first aspect of the invention in a sixth aspect of the invention, there is provided an isolated cell expressing the TCR of the first aspect of the invention.
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier, a TCR according to the first aspect of the invention, or a TCR complex according to the second aspect of the invention, Or the cell of the sixth aspect of the invention.
  • a method for treating a disease comprising administering an appropriate amount of the TCR according to the first aspect of the present invention, or the TCR complex of the second aspect of the present invention, or the present invention to a subject in need of treatment
  • the cell of the sixth aspect of the invention, or the pharmaceutical composition of the seventh aspect of the invention comprising administering an appropriate amount of the TCR according to the first aspect of the present invention, or the TCR complex of the second aspect of the present invention, or the present invention.
  • a method for the preparation of the T cell receptor of the first aspect of the invention comprising the steps of:
  • 1a and 1b are the amino acid sequence and DNA sequence of the single-stranded template TCR constructed in the present invention, respectively.
  • Figure 2a and Figure 2b show the amino acid sequence of the alpha variable domain and the amino acid sequence of the beta chain variable domain of the single-chain template TCR constructed in accordance with the present invention, respectively.
  • Figure 3 is an amino acid sequence of a linker of a single-stranded template TCR constructed according to the present invention.
  • Figures 4a-q show the alpha chain variable domain amino acid sequences of single-chain TCRs with high affinity for the ILSLELMKL-HLA A0201 complex, respectively, with the mutated residues underlined.
  • Figures 5a-m show the ⁇ -chain variable domain amino acid sequences of single-chain TCRs with high affinity for the ILSLELMKL-HLA A0201 complex, respectively, with the mutated residues underlined.
  • Figures 6a and 6b show the wild-type TCR alpha and beta chain variable domain amino acid sequences that specifically bind to the ILSLELMKL-HLA A0201 complex, respectively.
  • Figures 7a and 7b show the amino acid sequences of the reference TCR alpha and beta chains, respectively, in the present invention.
  • Figures 8a-q show the alpha chain variable domain amino acid sequence of a heterodimeric TCR having high affinity for the ILSLELMKL-HLA A0201 complex, respectively, the mutated residues are underlined.
  • Figures 9a-m show the ⁇ -chain variable domain amino acid sequence of a heterodimeric TCR having high affinity for the ILSLELMKL-HLA A0201 complex, respectively, and the mutated residues are underlined.
  • Figure 10a-m is the amino acid sequence of a fusion molecule of a high affinity single chain TCR with an anti-CD3 antibody.
  • Figure 11 is a plot of the affinity of wild-type TCR (i.e., reference TCR) versus the ILSLELMKL-HLA A0201 complex.
  • Figure 12a and Figure 12b show the amino acid sequences of the wild-type TCR alpha and beta chains of the present invention, respectively.
  • FIG. 14 Fusion of effector cells to antigen (RHAMM) mediated by fusion of anti-CD3 antibody with high affinity alpha beta heterodimeric TCR.
  • TCR T cell receptor
  • CDR3 ⁇ AATNSGYALN; and/or in three CDR regions of its ⁇ -chain variable domain
  • TCR T cell receptor
  • the International Immunogenetics Information System can be used to describe TCR.
  • the native alpha beta heterodimeric TCR has an alpha chain and a beta chain.
  • each strand comprises a variable region, a junction region, and a constant region
  • the beta strand typically also contains a short polymorphic region between the variable region and the junction region, but the polymorphic region is often considered part of the junction region.
  • the TCR junction region was determined by the unique IMGT TRAJ and TRBJ, and the constant region of the TCR was determined by the TACT and TRBC of IMGT.
  • Each variable region comprises three CDRs (complementarity determining regions), CDR1, CDR2 and CDR3, which are chimeric in the framework sequence.
  • CDR1, CDR2 and CDR3 which are chimeric in the framework sequence.
  • the different numbers of TRAV and TRBV refer to different V ⁇ types and V ⁇ types, respectively.
  • the alpha chain constant domain has the following symbols: TRAC*01, where "TR” represents the T cell receptor gene; "A” represents the alpha chain gene; C represents the constant region; "*01” represents the allele Gene 1.
  • the ⁇ -chain constant domain has the following symbols: TRBC1*01 or TRBC2*01, where “TR” represents a T cell receptor gene; “B” represents a ⁇ chain gene; C represents a constant region; “*01” represents an allele 1.
  • the constant region of the alpha chain is uniquely defined, and in the form of the beta strand, there are two possible constant region genes "C1" and "C2". Those skilled in the art can obtain constant region gene sequences of TCR alpha and beta chains by the disclosed IMGT database.
  • the framework sequences of the TCR variable domains (variable regions) of the invention may be murine or human, preferably of human origin.
  • TCR alpha chain variable domain refers to a linked TRAV and TRAJ region
  • TCR beta chain variable domain refers to a linked TRBV and TRBD/TRBJ region.
  • the three CDRs of the TCR alpha chain variable domain are CDR1 ⁇ , CDR2 ⁇ and CDR3 ⁇ , respectively; the three CDRs of the TCR ⁇ chain variable domain are CDR1 ⁇ , CDR2 ⁇ and CDR3 ⁇ , respectively.
  • the constant domain of TCR comprises an intracellular portion, a transmembrane region, and an extracellular portion.
  • the TCR of the invention preferably does not comprise a transmembrane region. More preferably, the amino acid sequence of the TCR of the present invention refers to the extracellular amino acid sequence of the TCR.
  • the ⁇ chain amino acid sequence and the ⁇ chain amino acid sequence of the "wild type TCR” described in the present invention are SEQ ID NO: 83 and SEQ ID NO: 84, respectively, as shown in Figs. 12a and 12b.
  • the ⁇ chain amino acid sequence and the ⁇ chain amino acid sequence of the "reference TCR” in the present invention are SEQ ID NO: 38 and SEQ ID NO: 39, respectively, as shown in Figs. 7a and 7b.
  • the alpha and beta chain variable domain amino acid sequences of the wild type TCR capable of binding to the ILSLELMKL-HLA A0201 complex are SEQ ID NO: 36 and SEQ ID NO: 37, respectively, as shown in Figures 6a and 6b.
  • the terms "polypeptide of the present invention", “TCR of the present invention”, and “T cell receptor of the present invention” are used interchangeably.
  • the TCR is a non-naturally occurring TCR.
  • the TCR is recombinant or isolated.
  • the present invention provides a T cell receptor (TCR) comprising a TCR alpha chain variable domain and a TCR beta chain variable domain.
  • TCR T cell receptor
  • the TCR alpha chain variable domain comprises:
  • the TCR ⁇ chain variable domain includes:
  • the TCR specifically binds to the ILSLELMKL-HLA A0201 complex.
  • the TCR is mutated at one or more amino acid residue positions selected from the group consisting of:
  • the binding affinity of the TCR to the ILSLELMKL-HLA A0201 complex is at least 2-fold greater than the binding affinity of the wild-type TCR to the ILSLELMKL-HLA A0201 complex (preferably, the wild type is relative to the mutant In the case of TCR, the TCR before the mutation).
  • the TCR comprises one or more mutations selected from the group consisting of:
  • the second R residue of CDR1 ⁇ is mutated to I, K or M, the third V residue is mutated to Y or L, the fourth S residue is mutated to N, and the sixth S residue is mutated to A;
  • the 1st position I residue of CDR2 ⁇ is mutated to L, the 3rd S residue is mutated to R, the 4th N residue is mutated to G, and the 6th D residue is mutated to S, or T;
  • the 5th S residue of CDR3 ⁇ is mutated to D, the 7th Y residue is mutated to I, the 8th A residue is mutated to H, I, V, or L, and the 9th L residue is mutated to M, I. , or F;
  • the first G residue of CDR1 ⁇ is mutated to P or L
  • the second T residue is mutated to H, S, R, or D
  • the third S residue is mutated to N, Y, or D
  • the fourth position is mutated to P, T, I, or L
  • the 5th P residue is mutated to R
  • the 6th N residue is mutated to L, A, or I;
  • the 4th position I residue of CDR2 ⁇ is mutated to V, and the 5th G residue is mutated to R;
  • the first A residue of CDR3 ⁇ is mutated to S, the second W residue is mutated to Y, and the third V residue is mutated to L.
  • the T cell receptor (TCR) comprises a TCR alpha chain variable domain and a TCR beta chain variable domain, said TCR beta chain variable domain comprising CDR1 beta, CDR2 beta, and CDR3 beta ,among them,
  • the CDR3 ⁇ comprises the sequence: DGAEQY and is 10 amino acid residues in length.
  • the DGAEQY is located at 5-10 of the CDR3 ⁇ . Bit.
  • the CDR3 ⁇ comprises the sequence: [3 ⁇ X1][3 ⁇ X2]S[3 ⁇ X3]DGAEQY, wherein [3 ⁇ X1], [3 ⁇ X2], [3 ⁇ X3] are independently selected from any natural amino acid Residues.
  • the [3 ⁇ X1] is A or S.
  • the [3 ⁇ X2] is W or Y.
  • the [3 ⁇ X3] is V or L.
  • the CDR3 ⁇ comprises a sequence selected from the group consisting of:
  • the CDR2[beta] comprises the sequence: SVG.
  • the CDR2 ⁇ comprises the sequence: SVG[2 ⁇ X1][2 ⁇ X2], wherein [2 ⁇ X1], [2 ⁇ X2] are independently selected from any natural amino acid residue.
  • the [2 ⁇ X1] is I or V.
  • the [2 ⁇ X2] is G or R.
  • the CDR2 ⁇ comprises a sequence selected from the group consisting of:
  • the CDR1 ⁇ comprises a sequence selected from the group consisting of:
  • GTSNPN LDDLRI (preferably), LRYIRA (preferably), LSNTRA and PHSPRL (preferably).
  • the T cell receptor (TCR) according to the invention comprises a TCR alpha chain variable domain and a TCR beta chain variable domain, said TCR alpha chain variable domain comprising CDR1 alpha, CDR2 alpha, and CDR3 alpha .
  • the CDR3 ⁇ comprises the sequence: AATN, and the CDR3 ⁇ is 8-13 amino acids in length, preferably 11 amino acids.
  • the CDR3 ⁇ comprises the sequence: AATN[3 ⁇ X1]G[3 ⁇ X2]S[3 ⁇ X3][3 ⁇ X4]N, wherein [3 ⁇ X1], [3 ⁇ X2], [3 ⁇ X3] are independently selected From any natural amino acid residue.
  • the [3 ⁇ X1] is S or D.
  • the [3 ⁇ X2] is Y or I.
  • the [3 ⁇ X3] is A, I, H or V.
  • the CDR3 ⁇ comprises a sequence selected from the group consisting of:
  • AATNDGIHIN, AATNDGIIFN, AATNDGIIIN preferably), AATNDGILIN (preferably), AATNDGYHMN (preferably), AATNDGYVMN (preferably) and AATNSGYALN.
  • the CDR2 ⁇ comprises the sequence: [2 ⁇ X1]Y[2 ⁇ X2][2 ⁇ X3]G[2 ⁇ X4], wherein [2 ⁇ X1], [2 ⁇ X2], [2 ⁇ X3], [2 ⁇ X4] are independent It is selected from any natural amino acid residue.
  • the [2 ⁇ X1] is I or L.
  • the [2 ⁇ X2] is S or R.
  • the [2 ⁇ X3] is N or G.
  • the [2 ⁇ X4] is D, S or T.
  • the CDR2 ⁇ comprises a sequence selected from the group consisting of:
  • IYRNGT preferably
  • LYRGGS preferably
  • IYSNGD IYRNGT
  • the CDR1 ⁇ comprises the sequence: D[1 ⁇ X1][1 ⁇ X2][1 ⁇ X3]Q[1 ⁇ X4], wherein [1 ⁇ X1], [1 ⁇ X2], [1 ⁇ X3], [1 ⁇ X4] are independent It is selected from any natural amino acid residue.
  • the [1 ⁇ X1] is I, M, K, or R.
  • the [1 ⁇ X2] is Y, L or V.
  • the [1 ⁇ X3] is N, or S.
  • the [1 ⁇ X4] is S or A.
  • the CDR1 ⁇ comprises a sequence selected from the group consisting of:
  • DIYNQS (best, with the highest affinity), DIYNQA (preferably), DKLNQS, DMLNQS (preferably), and DRVSQS.
  • the TCR according to the present invention has a particularly high affinity when the amino acid sequence of the CDR1 ⁇ position of the TCR ⁇ chain variable domain is DIYNQS.
  • the T cell receptor (TCR) according to the invention comprises a TCR alpha chain variable domain and a TCR beta chain variable domain, and the CDR1 alpha of the TCR alpha chain variable domain comprises the sequence: DIYNQS .
  • the TCR alpha chain variable domains of the TCRs do not simultaneously comprise the following CDRs:
  • CDR1 ⁇ DRVSQS
  • CDR2 ⁇ IYSNGD
  • CDR3 ⁇ AATNSGYALN.
  • the TCR ⁇ chain variable domains of the TCRs do not simultaneously comprise the following CDRs:
  • CDR1 ⁇ GTSNPN
  • CDR2 ⁇ SVGIG
  • CDR3 ⁇ AWSVDGAEQY.
  • the position numbers of the amino acid sequences of TRAC*01 and TRBC1*01 or TRBC2*01 are numbered in order from N-terminal to C-terminal, such as TRBC1*01 or TRBC2*01, according to N.
  • the 60th amino acid in the order from the end to the C-end is P (valine), which can be described as Pro60 of TRBC1*01 or TRBC2*01 exon 1 in the present invention, and can also be expressed as TRBC1* 01 or TRBC2*01, the 60th amino acid of exon 1, and TRBC1*01 or TRBC2*01, the 61st amino acid is Q (glutamine) in order from N to C.
  • the position numbers of the amino acid sequences of the variable regions TRAV and TRBV are numbered according to the positions listed in the IMGT.
  • the position number listed in IMGT is 46, which is described in the present invention as amino acid 46 of TRAV, and so on.
  • special instructions will be given.
  • tumor is meant to include all types of cancer cell growth or carcinogenic processes, metastatic tissues or malignant transformed cells, tissues or organs, regardless of pathological type or stage of infection.
  • tumors include, without limitation, solid tumors, soft tissue tumors, and metastatic lesions.
  • solid tumors include: malignant tumors of different organ systems, such as sarcoma, lung squamous cell carcinoma, and cancer.
  • sarcoma a malignant tumors of different organ systems
  • lung squamous cell carcinoma include cancer.
  • Squamous cell carcinoma of the lung includes malignant tumors, for example, most colon cancer, rectal cancer, renal cell carcinoma, liver cancer, non-small cell cancer of the lung, small intestine cancer and esophageal cancer. Metastatic lesions of the above cancers can likewise be treated and prevented using the methods and compositions of the invention.
  • the alpha chain variable domain and the beta chain variable domain of TCR each contain three CDRs, similar to the complementarity determining regions of antibodies.
  • CDR3 interacts with an antigenic short peptide
  • CDR1 and CDR2 interact with HLA.
  • the CDR of the TCR molecule determines its interaction with the antigenic short peptide-HLA complex.
  • the present inventors have found for the first time that the ⁇ -chain variable domain amino acid sequence and the ⁇ -chain variable domain amino acid sequence of the wild-type TCR capable of binding to the antigen short peptide ILSLELMKL and HLA A0201 complex (ie, ILSLELMKL-HLAA0201 complex) are SEQ ID NO, respectively. :36 and SEQ ID NO:37. It has the following CDR regions:
  • the present invention obtains a high affinity TCR which has an affinity for the ILSLELMKL-HLA A0201 complex to be at least 2 times the affinity of the wild type TCR and the ILSLELMKL-HLA A0201 complex by mutation screening of the above CDR regions.
  • the present invention provides a T cell receptor (TCR) having an activity of binding to the ILSLELMKL-HLA A0201 complex.
  • the TCR of the present invention comprises an ⁇ chain variable domain and a ⁇ chain variable domain, the TCR ⁇ chain variable domain comprises 3 CDR regions and the TCR ⁇ chain variable domain comprises 3 CDR regions, and the TCR is in the ⁇ chain variable domain 3 CDR regions
  • AATNSGYALN contains at least one of the following mutations:
  • TCR is in the three CDR regions of the ⁇ -chain variable domain
  • AWSVDGAEQY contains at least one of the following mutations:
  • the number of mutations in the CDR region of the TCR ⁇ chain is 3 or 4 or 6 or 7 or 8 or 9 or 11; and/or the number of mutations in the CDR region of the TCR ⁇ chain is 2 or 3 or 5 or 6 or 7 or 8 or 9.
  • the TCR of the present invention is an ⁇ heterodimeric TCR
  • the ⁇ chain variable domain of the TCR comprises at least 90% of the amino acid sequence shown in SEQ ID NO: 36 (eg, may be at least 91%, 92) Amino acid sequence of sequence homology of %, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence homology; and/or the ⁇ chain variable domain of the TCR comprises At least 90% (e.g., may be at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%) identical to the amino acid sequence set forth in SEQ ID NO:37 Amino acid sequence of sequence homology.
  • the TCR comprises (i) all or part of a TCR alpha chain other than its transmembrane domain, and (ii) all or part of a TCR beta chain other than its transmembrane domain, wherein (i) and (ii) Each comprises a variable domain of the TCR chain and at least a portion of the constant domain.
  • the three CDRs of the wild type TCR alpha chain variable domain SEQ ID NO: 36, CDR1, CDR2 and CDR3, are located at positions 27-32, 50-55 and 90-99 of SEQ ID NO: 36, respectively.
  • the amino acid residue number is the number shown in SEQ ID NO: 36
  • 28R is the second position R of CDR1 ⁇
  • 29V is the third position V of CDR1 ⁇
  • 30S is the fourth position S of CDR1 ⁇
  • 32S is It is the 6th position S of CDR1 ⁇
  • 50I is the 1st position I of CDR2 ⁇
  • 52S is the 3rd position S of CDR2 ⁇
  • 53N is the 4th position N of CDR2 ⁇
  • 55D is the 6th position D of CDR2 ⁇
  • 94S is Is the 5th S of CDR3 ⁇
  • 96Y is the 7th position Y of CDR3 ⁇
  • 97A is the 8th position A of CDR3 ⁇
  • 98L is C
  • the three CDRs of the wild type TCR ⁇ chain variable domain SEQ ID NO: 37, CDR1, CDR2 and CDR3, are located at positions 27-32, 50-54 and 92 of SEQ ID NO: 37, respectively. -101.
  • the amino acid residue number is the number shown in SEQ ID NO: 37
  • 27G is the first position G of CDR1 ⁇
  • 28T is the second position T of CDR1 ⁇
  • 29S is the third position S of CDR1 ⁇
  • 30N is The fourth position N
  • 31P of CDR1 ⁇ is the 5th position P of CDR1 ⁇
  • 32N is the 6th position N of CDR1 ⁇
  • 53I is the 4th position of CDR2 ⁇
  • 54G is the 5th position G of CDR2 ⁇
  • 92A is The first position A
  • 93W of CDR3 ⁇ is the second position W of CDR3 ⁇
  • 95V is the fourth position V of CDR3 ⁇ .
  • the present invention provides a TCR having the property of binding to the ILSLELMKL-HLA A0201 complex and comprising a TCR alpha chain variable domain and a TCR beta chain variable domain, wherein the TCR is variable in the alpha chain shown in SEQ ID NO: A mutation occurs in the domain, the mutated amino acid residue site comprising one or more of 28R, 29V, 30S, 32S, 50I, 52S, 53N, 55D, 94S, 96Y, 97A or 98L, wherein the amino acid residue
  • the numbering uses the number shown in SEQ ID NO: 36; and/or the TCR is mutated in the ⁇ -chain variable domain of SEQ ID NO: 37, the mutated amino acid residue sites including 27G, 28T, One or more of 29S, 30N, 31P, 32N, 53I, 54G, 92A, 93W or 95V, wherein the amino acid residue numbering is the number shown in SEQ ID NO:37.
  • the mutated TCR alpha chain variable domain comprises one or more amino acid residues selected from the group consisting of: 28I, 28K, or 28M; 29Y or 29L; 30N; 32A; 50L; 52R; 53G; 55S or 55T; 94D; 96I; 97H, 97I, 97V or 97L; 98M, 98I or 98F; and/or the mutated TCR ⁇ chain variable domain comprises one or more selected from the group consisting of Amino acid residues: 27P or 27L; 28H, 28S, 28R or 28D; 29N, 29Y or 29D; 30P, 30T, 30I or 30L; 31R; 32L, 32A or 32I; 53V; 54R; 92S; 93Y; 95L.
  • the Thr48 of the wild type TCR alpha chain constant region TRAC*01 exon 1 was mutated to cysteine according to the method of site-directed mutagenesis well known to those skilled in the art, and the ⁇ -chain constant region TRBC1*01 or TRBC2*01 exon 1 was mutated.
  • the Ser57 is mutated to cysteine, which gives a reference TCR, the amino acid sequences of which are shown in Figures 7a and 7b, respectively, and the mutated cysteine residues are indicated by bold letters.
  • the above cysteine substitution can form an artificial interchain disulfide bond between the constant regions of the reference TCR and the ⁇ chain to form a more stable soluble TCR, thereby making it easier to evaluate the complexation of TCR with ILSLELMKL-HLA A0201. Binding affinity and/or binding half-life between the substances. It will be appreciated that the CDR regions of the TCR variable region determine its affinity for the pMHC complex and, therefore, the cysteine substitution of the above TCR constant region does not affect the binding affinity and/or binding half-life of the TCR.
  • the measured binding affinity between the reference TCR and the ILSLELMKL-HLA A0201 complex is considered to be the binding affinity between the wild-type TCR and the ILSLELMKL-HLA A0201 complex, ie, as described in the present invention.
  • the binding affinity between the wild-type TCR and the ILSLELMKL-HLA A0201 complex is equivalent to the binding affinity between the reference TCR and the ILSLELMKL-HLA A0201 complex.
  • the binding affinity between the TCR of the invention and the ILSLELMKL-HLA A0201 complex is determined to be at least 10 times the binding affinity between the reference TCR and the ILSLELMKL-HLA A0201 complex, ie equivalent to the TCR and ILSLELMKL of the invention
  • the binding affinity between the -HLA A0201 complex is at least 10-fold greater than the binding affinity between the wild-type TCR and the ILSLELMKL-HLA A0201 complex.
  • Binding may be measured by any suitable method, the affinity (dissociation equilibrium constant and inversely proportional to K D) and half-life of binding (expressed as T 1/2). It should be understood that doubling the affinity of the TCR will result in a halving of K D . T 1/2 is calculated as In2 divided by the dissociation rate (K off ). Therefore, doubling T 1/2 will cause K off to be halved.
  • the same test protocol is used to detect the binding affinity or binding half-life of a given TCR several times, for example 3 or more times, and the average of the results is taken. In a preferred embodiment, these measurements are performed using the surface plasmon resonance (BIAcore) method of the present invention.
  • the method of detecting the reference dissociation equilibrium constant K D is 270 m Solution TCR of ILSLELMKL-HLA A0201 complex than the present invention, i.e., that of wild-type TCR understanding of ILSLELMKL-HLA A0201 complex dissociation equilibrium constant K D is also 270 ⁇ M. Since the doubling of the affinity of the TCR will result in a halving of K D , if the dissociation equilibrium constant K D of the high affinity TCR to the ILSLELMKL-HLA A0201 complex is detected to be 27 ⁇ M, the high affinity TCR is described for the ILSLELMKL-HLA A0201 complex.
  • the affinity is 10 times the affinity of the wild-type TCR for the ILSLELMKL-HLA A0201 complex.
  • the binding affinity of the TCR to the ILSLELMKL-HLA A0201 complex is at least 2 times the binding affinity of the wild-type TCR to the ILSLELMKL-HLA A0201 complex using a preferred assay of the invention; At least 5 times; more preferably at least 10 times.
  • the binding affinity of the TCR to the ILSLELMKL-HLA A0201 complex is at least 100 times greater than the binding affinity of the wild-type TCR to the ILSLELMKL-HLA A0201 complex using a preferred assay of the invention; Preferably at least 10 3 fold; more preferably, at least 10 4 fold; most preferably, the binding affinity of the TCR of the invention to the ILSLELMKL-HLA A0201 complex is 10 5 of the binding affinity of the wild-type TCR to the ILSLELMKL-HLA A0201 complex. -10 6 times.
  • the present invention detects preferred embodiment, the solution of the TCR ILSLELMKL-HLA A0201 complex dissociation equilibrium constant K D ⁇ 100 ⁇ M; Preferably, 10 ⁇ M ⁇ K D ⁇ 100 ⁇ M; More preferably, [mu] M ⁇ K D ⁇ 10 ⁇ M.
  • the dissociation equilibrium constant K D of the TCR to the ILSLELMKL-HLA A0201 complex is ⁇ 1 ⁇ M using a preferred detection mode of the invention; preferably, 10 nM ⁇ K D ⁇ 1 ⁇ M; more preferably, 100 pM ⁇ K D ⁇ 10 nM.
  • Mutations can be carried out by any suitable method, including but not limited to those based on polymerase chain reaction (PCR), restriction enzyme-based cloning or linkage-independent cloning (LIC) methods. Many standard molecular biology textbooks detail these methods. For more details on polymerase chain reaction (PCR) mutagenesis and cloning based on restriction enzymes, see Sambrook and Russell, (2001) Molecular Cloning-A Laboratory Manual (Third Edition) CSHL Publishing house. More information on the LIC method can be found (Rashtchian, (1995) Curr Opin Biotechnol 6(1): 30-6).
  • PCR polymerase chain reaction
  • LIC linkage-independent cloning
  • the method of producing the TCR of the present invention may be, but is not limited to, screening for a TCR having high affinity for the ILSLELMKL-HLA A0201 complex from a diverse library of phage particles displaying such TCR, as in the literature (Li, et al ( 2005) Nature Biotech 23(3): 349-354).
  • genes expressing wild-type TCR alpha and beta chain variable domain amino acids or genes expressing the alpha and beta chain variable domain amino acids of the slightly modified wild-type TCR can be used to prepare template TCRs.
  • the changes required to produce the high affinity TCR of the invention are then introduced into the DNA encoding the variable domain of the template TCR.
  • the TCR of the invention is mutated in the alpha chain variable domain of SEQ ID NO: 36, the mutated amino acid residue sites comprising 28R, 29V, 30S, 32S, 50I Or one or more of 52S, 53N, 55D, 94S, 96Y, 97A or 98L, wherein the amino acid residue numbering is the number shown in SEQ ID NO: 36; and/or the TCR is in SEQ ID NO: 37 Mutations occur in the indicated beta chain variable domains, which include 27G, 28T, 29S, One or more of 30N, 31P, 32N, 53I, 54G, 92A, 93W or 95V, wherein the amino acid residue numbering is the number shown in SEQ ID NO:37.
  • the mutated TCR alpha chain variable domain comprises one or more amino acid residues selected from the group consisting of: 28I, 28K, or 28M; 29Y or 29L; 30N; 32A; 50L; 52R; 53G; 55S or 55T 94D; 96I; 97H, 97I, 97V or 97L; 98M, 98I or 98F; and/or the mutated TCR ⁇ chain variable domain comprises one or more amino acid residues selected from the group consisting of: 27P or 27L; 28H, 28S, 28R or 28D; 29N, 29Y or 29D; 30P, 30T, 30I or 30L; 31R; 32L, 32A or 32I; 53V; 54R; 92S; 93Y; 95L.
  • specific forms of the mutation in the alpha chain variable domain include R28I/K/M, V29Y/L, S30N, S32A, I50L, S52R, N53G, D55S/T, S94D, Y96I, A97H/I/V One or more groups in /L or L98M/I/F; specific forms of the mutation in the ⁇ -chain variable domain include G27P/L, T28H/S/R/D, S29N/Y/D, N30P/T One or several groups of /I/L, P31R, N32L/A/I, I53V, G54R, A92S, W93Y or V95L.
  • the high affinity TCR of the invention comprises an alpha chain variable domain amino acid sequence of SEQ ID NO: 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54
  • the TCR alpha chain of the alpha chain variable domain amino acid sequence (SEQ ID NO: 36) containing the wild-type TCR can comprise SEQ ID NO: 57, 58, 59, 60, 61, 62, 63, 64, 65, 66
  • the TCR beta chains of one of 67, 68 and 69 combine to form a heterodimeric TCR or single chain TCR molecule.
  • the TCR ⁇ chain comprising the ⁇ -variable domain amino acid sequence of wild-type TCR can comprise SEQ ID NO: 40, 41, 42, 43, 44, 45, 46, 47, 48, 49,
  • the TCR alpha chains of one of 50, 51, 52, 53, 54, 55 and 56 combine to form a heteromeric TCR or single chain TCR molecule.
  • TCR alpha chain comprising one of the TCR alpha chain variable domain amino acid sequences SEQ ID NO: 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 and 56
  • the TCR alpha chain can be combined with a TCR beta chain comprising one of the TCR beta chain variable domain amino acid sequences SEQ ID NO: 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68 and 69.
  • a TCR of the invention is a moiety having at least one TCR alpha and/or TCR beta chain variable domain. They usually comprise both a TCR alpha chain variable domain and a TCR beta chain variable domain. They may be alpha beta heterodimers or single stranded forms or any other form that is stable. In adoptive immunotherapy, the full length strand of the alpha beta heterodimeric TCR (including the cytoplasmic and transmembrane domains) can be transfected.
  • the TCR of the present invention can be used as a targeting agent for delivering a therapeutic agent to an antigen presenting cell or in combination with other molecules to prepare a bifunctional polypeptide to direct effector cells, in which case the TCR is preferably in a soluble form.
  • the TCR of the invention may be a TCR that introduces an artificial interchain disulfide bond between the residues of its alpha and beta chain constant domains.
  • the cysteine residue forms an artificial interchain disulfide bond between the alpha and beta chain constant domains of the TCR.
  • a cysteine residue can replace other amino acid residues at a suitable position in the native TCR to form an artificial interchain disulfide bond.
  • a Thr248 of the exon 1 of TRAC*01 is substituted and Ser57 of exon 1 of TRBC1*01 or TRBC2*01 is substituted to form a disulfide bond.
  • Other sites for introducing a cysteine residue to form a disulfide bond may also be: Thr45 of TRAC*01 exon 1 and Ser77 of TRBC1*01 or TRBC2*01 exon 1; TRAC*01 exon 1 of Tyr10 and TRBC1*01 or TRBC2*01 exon 1 of Ser17; TRAC*01 exon 1 of Thr45 and TRBC1*01 or TRBC2*01 exon 1 Asp59; Ser15 of TRAC*01 exon 1 and Glu15 of exon 1 of TRBC2*01; Arg53 of TRAC*01 exon 1 and Ser54 of TRBC1*01 or TRBC2*01 exon 1 ; Pro89 and TRBC1*01 of exon 1 of TRAC*01 or Ala19 of exon 1 of TRBC2*01;
  • a cysteine residue replaces any of the above-mentioned sites in the ⁇ and ⁇ chain constant domains.
  • a maximum of 15, or a maximum of 10, or a maximum of 8 or fewer amino acids may be truncated at one or more C-termini of the TCR constant domain of the invention such that it does not include a cysteine residue to achieve deletion of the native
  • the purpose of the interchain disulfide bond can also be achieved by mutating a cysteine residue forming a natural interchain disulfide bond to another amino acid.
  • the TCR of the present invention may comprise an artificial interchain disulfide bond introduced between residues of its ⁇ and ⁇ chain constant domains.
  • the constant domains may or may not contain the introduced artificial disulfide bonds as described above, and the TCRs of the present invention may each contain alpha and beta chain constant domain sequences.
  • the alpha and beta chain constant domain sequences of TCR can be joined by a natural interchain disulfide bond present in the TCR.
  • Patent Document 201510260322.4 also discloses that introduction of an artificial interchain disulfide bond between the ⁇ chain variable region of the TCR and the ⁇ chain constant region can significantly improve the stability of the TCR. Therefore, the ⁇ chain variable region of the high affinity TCR of the present invention and the ⁇ chain constant region may further contain an artificial interchain disulfide bond.
  • cysteine residue forming an artificial interchain disulfide bond between the ⁇ chain variable region of the TCR and the ⁇ chain constant region is substituted with: amino acid 46 of TRAV and TRBC1*01 or TRBC2* 01 amino acid at position 60 of exon 1; amino acid at position 47 of TRAV and amino acid at position 61 of exon 1 of TRBC1*01 or TRBC2*01; amino acid at position 46 of TRAV and TRBC1*01 or TRBC2*01 The amino acid at position 61 of the 1st; or the amino acid at position 47 of TRAV and the amino acid at position 60 of exon 1 of TRBC1*01 or TRBC2*01.
  • such a TCR may comprise (i) all or part of a TCR alpha chain other than its transmembrane domain, and (ii) all or part of a TCR beta chain other than its transmembrane domain, wherein (i) and (ii) Both comprise a variable domain of the TCR chain and at least a portion of the constant domain, the alpha chain forming a heterodimer with the beta chain. More preferably, such a TCR may comprise an alpha chain variable domain and a beta chain variable domain and all or part of a beta chain constant domain other than a transmembrane domain, but which does not comprise an alpha chain constant domain, said TCR alpha The chain variable domain forms a heterodimer with the beta chain.
  • the TCR of the present invention further comprises a TCR having a mutation in its hydrophobic core region, and the mutation of these hydrophobic core regions is preferably a mutation capable of increasing the stability of the TCR of the present invention, as in the publication number It is described in the patent document of WO2014/206304.
  • Such a TCR can be mutated at its position in the following variable domain hydrophobic core: (alpha and/or beta chain) variable region amino acids 11, 13, 19, 21, 53, 76, 89, 91, 94, and / Or the ⁇ -chain J gene (TRAJ) short peptide amino acid position reciprocal position 3, 5, 7 and/or ⁇ chain J gene (TRBJ) short peptide amino acid position reciprocal position 2, 4, 6 where the amino acid sequence position number The location number listed in the International Immunogenetics Information System (IMGT).
  • IMGT International Immunogenetics Information System
  • the TCR in which the hydrophobic core region is mutated in the present invention may be a high-stability single-chain TCR composed of a flexible peptide chain linking the variable domains of the ⁇ and ⁇ chains of the TCR.
  • the CDR region of the TCR variable region determines its affinity for the short peptide-HLA complex, and the hydrophobic core mutation can make the TCR more stable, but does not affect its affinity with the short peptide-HLA complex.
  • the flexible peptide chain of the present invention may be any peptide chain suitable for linking the TCR alpha and beta chain variable domains.
  • the template strand for screening high-affinity TCRs constructed in Example 1 of the present invention is the above-described high-stability single-chain TCR containing a hydrophobic core mutation.
  • TCR and ILSLELMKL-HLA A0201 complexes can be more conveniently evaluated using a more stable TCR Affinity between.
  • the CDR regions of the alpha chain variable domain and the beta chain variable domain of the single chain template TCR are identical to the CDR regions of the wild type TCR. That is, the three CDRs of the ⁇ chain variable domain are CDR1 ⁇ : DRVSQS, CDR2 ⁇ : IYSNGD, CDR3 ⁇ : AATNSGYALN; the three CDRs of the ⁇ chain variable domain are CDR1 ⁇ : GTSNPN, CDR2 ⁇ : SVGIG, CDR3 ⁇ : AWSVDGAEQY, respectively.
  • the amino acid sequence (SEQ ID NO: 1) and nucleotide sequence (SEQ ID NO: 2) of the single-stranded template TCR are shown in Figures 1a and 1b, respectively.
  • the three CDRs of the single-chain template TCR alpha chain variable domain SEQ ID NO: 3, CDR1, CDR2 and CDR3, are located at positions 27-32, 50-55 and 90-99 of SEQ ID NO: 3, respectively.
  • Bit. the amino acid residue number is the number shown in SEQ ID NO: 3, 28R is the second position R of CDR1 ⁇ , 29V is the third position V of CDR1 ⁇ , and 30S is the fourth position S of CDR1 ⁇ , 32S is It is the 6th position S of CDR1 ⁇ , 50I is the 1st position I of CDR2 ⁇ , 52S is the 3rd position S of CDR2 ⁇ , 53N is the 4th position N of CDR2 ⁇ , 55D is the 6th position D of CDR2 ⁇ , 94S is It is the 5th position S of CDR3 ⁇ , 96Y is the 7th position Y of CDR3 ⁇ , 97A is the 8th position A of CDR3 ⁇ , and 98L is the 9th position L of CDR3
  • the three CDRs of the single-chain template TCR ⁇ chain variable domain SEQ ID NO: 4, ie, CDR1, CDR2 and CDR3 are located at positions 27-32, 50-54 and SEQ ID NO: 4, respectively. 92-101.
  • the amino acid residue number is the number shown in SEQ ID NO: 4, 27G is the first position G of CDR1 ⁇ , 28T is the second position T of CDR1 ⁇ , and 29S is the third position S of CDR1 ⁇ , 30N is The fourth position N, 31P of CDR1 ⁇ is the 5th position P of CDR1 ⁇ , 32N is the 6th position N of CDR1 ⁇ , 53I is the 4th position of CDR2 ⁇ , and 54G is the 5th position G of CDR2 ⁇ , 92A is The first position A, 93W of CDR3 ⁇ is the second position W of CDR3 ⁇ , and 95V is the fourth position V of CDR3 ⁇ .
  • the ⁇ heterodimer of the present invention having high affinity for the ILSLELMKL-HLA A0201 complex is obtained by transferring the CDR regions of the selected high-affinity single-stranded TCR to the wild type by site-directed mutagenesis.
  • the TCR alpha chain variable domain (SEQ ID NO: 36) is obtained from the corresponding position of the beta chain variable domain (SEQ ID NO: 37).
  • the alpha-chain variable domain hydrophobic core amino acid residue 19A of the TCR of the invention is employed, using the numbering set forth in SEQ ID NO: 36 (ie, the 19th position of the alpha chain variable region listed in IMGT) , 21L (ie, the 21st position of the alpha chain variable region listed in IMGT) and 79S (ie, the 94th position of the alpha chain variable region listed in IMGT) have one or more mutations and/or SEQ ID NO: 37, the TCR ⁇ chain variable domain hydrophobic core amino acid residue 13Q (ie, the 13th position of the ⁇ chain variable region listed in IMGT), 19L (ie, the ⁇ chain listed in IMGT can be Variable region 19th), 64L (ie, 76th position of the beta chain variable region listed in IMGT), 78S (ie, 91th position of the beta chain variable region listed in IMGT) and 81L (ie listed in IMGT)
  • the alpha chain variable domain hydrophobic core of the invention comprises one or more of amino acid residues 119V, 21I and 79I, using the numbering set forth in SEQ ID NO:36. / or using the number shown in SEQ ID NO: 37
  • the TCR ⁇ variable domain hydrophobic core comprises one or more of amino acid residues 13V, 19V, 64Y, 78I and 81V.
  • the mutated form of the TCR ⁇ variable domain hydrophobic core comprises one or more of A19V, L21I and S79I; the mutant forms of the TCR ⁇ variable domain hydrophobic core include Q13V, L19V, L64Y, S78I and L81V One or several groups in .
  • the high affinity TCR of the present invention further comprises an alpha chain variable domain amino acid sequence of SEQ ID NO: 6, 7, 8, Amino acid sequences of one of 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 and 22 and/or ⁇ chain variable domain SEQ ID NO: 23, 24, 25, 26 One of 27, 28, 29, 30, 31, 32, 33, 34 and 35.
  • SEQ ID NO: 3 as a template strand can be SEQ ID NO: 23, 24, 25, 26, 27, 28, 29, 30, 31 with the amino acid sequence.
  • the TCR ⁇ chain variable domains of 32, 33, 34 or 35 are combined to form the single chain TCR molecule.
  • the above-described high-stability single-chain TCR ⁇ chain variable domain (SEQ ID NO: 4) as a template strand may be SEQ ID NO: 6, 7, 8, 9, 10, 11, 12, 13, 14 with amino acid sequences.
  • the TCR alpha chain variable domains of 15, 16, 17, 18, 19, 20, 21 or 22 are combined to form the single chain TCR molecule.
  • the TCR alpha chain variable domain SEQ ID NO: 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 or 22 is variable with the TCR ⁇ chain
  • the domain SEQ ID NO: 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34 or 35 combines to form the single chain TCR molecule.
  • the amino acid sequences of the ⁇ -chain variable domain and the ⁇ -chain variable domain of the high-affinity single-chain TCR molecule are preferably selected from the following Table 1:
  • the TCR of the present invention can also be provided in the form of a multivalent complex.
  • the multivalent TCR complex of the present invention comprises a polymer formed by combining two, three, four or more TCRs of the present invention, such as a tetrameric domain of p53 to produce a tetramer, or more A complex formed by combining a TCR of the invention with another molecule.
  • the TCR complexes of the invention can be used to track or target cells that present a particular antigen in vitro or in vivo, as well as intermediates that produce other multivalent TCR complexes for such applications.
  • the TCR of the present invention may be used singly or in combination with the conjugate in a covalent or other manner, preferably in a covalent manner.
  • the conjugate comprises a detectable label (for diagnostic purposes, wherein the TCR is used to detect the presence of a cell presenting the ILSLELMKL-HLA A0201 complex), a therapeutic agent, a PK (protein kinase) modified moiety or any of these substances The combination is combined or coupled.
  • Detectable labels for diagnostic purposes include, but are not limited to, fluorescent or luminescent labels, radioactive labels, MRI (magnetic resonance imaging) or CT (electron computed tomography) contrast agents, or capable of producing detectable products Enzyme.
  • Therapeutic agents that can be combined or coupled to the TCRs of the invention include, but are not limited to: 1. Radionuclides (Koppe et al, 2005, Cancer metastasis reviews 24, 539); 2. Biotoxicity (Chaudhary et al, 1989) , Nature 339, 394; Epel et al, 2002, Cancer Immunology and Immunotherapy 51, 565); 3. Cytokines such as IL-2, etc.
  • liposomes (Mamot et al, 2005, Cancer research 65, 11631); 9. nanomagnetic particles; 10. prodrug activating enzymes (eg, DT-diaphorase) (DTD) or biphenyl hydrolase-like protein (BPHL); 11. chemotherapeutic agent (eg, cisplatin) or any form of nanoparticles, and the like.
  • prodrug activating enzymes eg, DT-diaphorase) (DTD) or biphenyl hydrolase-like protein (BPHL)
  • chemotherapeutic agent eg, cisplatin or any form of nanoparticles, and the like.
  • the antibody or fragment thereof to be combined with the TCR of the present invention includes an anti-T cell or an NK-cell determining antibody, such as an anti-CD3 or an anti-CD28 or an anti-CD16 antibody, and the binding of the above antibody or a fragment thereof to the TCR can effect the effector cell. Orientation to better target target cells.
  • a preferred embodiment is the TCR and anti-drug of the present invention.
  • - CD3 antibody or a functional fragment or variant of the anti-CD3 antibody binds.
  • the fusion molecule of the TCR of the present invention and the anti-CD3 single-chain antibody comprises a TCR ⁇ chain variable domain amino acid sequence selected from the group consisting of SEQ ID NOs: 6, 7, 8, 9, 10, 11, 12, 13, 14 , 15, 16, 17, 18, 19, 20, 21, 22, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56 And a TCR ⁇ chain variable domain amino acid sequence selected from the group consisting of SEQ ID NOs: 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 57, 58, 59, 60 , 61, 62, 63, 64, 65, 66, 67, 68, 69.
  • the amino acid sequence of the high affinity single chain TCR molecule of the invention and the anti-CD3 single chain antibody fusion molecule is selected from the group consisting of SEQ ID NOs: 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80 , 81, 82.
  • the invention also relates to nucleic acid molecules encoding the TCRs of the invention.
  • the nucleic acid molecule of the invention may be in the form of DNA or in the form of RNA.
  • the DNA can be a coding strand or a non-coding strand.
  • a nucleic acid sequence encoding a TCR of the invention may be the same or a degenerate variant of the nucleic acid sequence set forth in the Figures of the invention.
  • degenerate variant refers in the present invention to a protein sequence having SEQ ID NO: 1, but to the sequence of SEQ ID NO: Differential nucleic acid sequences.
  • the full length sequence of the nucleic acid molecule of the present invention or a fragment thereof can generally be obtained by, but not limited to, PCR amplification, recombinant methods or synthetic methods. At present, it has been possible to obtain a DNA sequence encoding the TCR (or a fragment thereof, or a derivative thereof) of the present invention completely by chemical synthesis. The DNA sequence can then be introduced into various existing DNA molecules (or vectors) and cells known in the art.
  • the invention also relates to vectors comprising the nucleic acid molecules of the invention, as well as host cells genetically engineered using the vectors or coding sequences of the invention.
  • the invention also encompasses isolated cells, particularly T cells, which express the TCR of the invention.
  • isolated cells particularly T cells, which express the TCR of the invention.
  • T cells There are a number of methods suitable for T cell transfection with DNA or RNA encoding the high affinity TCR of the invention (e.g., Robbins et al., (2008) J. Immunol. 180: 6116-6131).
  • T cells expressing the high affinity TCR of the invention can be used in adoptive immunotherapy.
  • Those skilled in the art will be aware of many suitable methods for performing adoptive therapy (e.g., Rosenberg et al., (2008) Nat Rev Cancer 8(4): 299-308).
  • the present invention also provides a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a TCR of the present invention, or a TCR complex of the present invention, or a cell which presents the TCR of the present invention.
  • the invention also provides a method of treating a disease comprising administering to a subject in need of treatment an appropriate amount of a TCR of the invention, or a TCR complex of the invention, or a cell presenting a TCR of the invention, or a pharmaceutical composition of the invention.
  • amino acid names in this article are identified by the international common single letter, and the corresponding amino acid names are abbreviated as: Ala (A), Arg (R), Asn (N), Asp (D), Cys (C), Gln(Q), Glu(E), Gly(G), His(H), Ile(I), Leu(L), Lys(K), Met(M), Phe(F), Pro (P), Ser(S), Thr(T), Trp(W), Tyr(Y), Val(V); in the present invention, Pro60 or 60P means the 60th proline, and so on.
  • R28I represents that the R at position 28 is substituted by I
  • R28I/K/M represents that the R at position 28 is substituted by I or by K. Substituted or replaced by M. Others and so on.
  • the TCR of the present invention further includes up to five TCRs of the present invention, preferably to More than 3, more preferably up to 2, optimally 1 amino acid (especially amino acids located outside of the CDR regions), replaced by amino acids of similar or similar nature, and still retain their functional TCR.
  • the present invention also encompasses a TCR slightly modified for the TCR of the present invention.
  • Modifications include: chemically derivatized forms of the TCRs of the invention, such as acetylation or carboxylation.
  • Modifications also include glycosylation, such as those produced by glycosylation modifications in the synthesis and processing of the TCRs of the invention or in further processing steps. Such modification can be accomplished by exposing the TCR to an enzyme that performs glycosylation, such as a mammalian glycosylation enzyme or a deglycosylation enzyme.
  • Modified forms also include sequences having phosphorylated amino acid residues such as phosphotyrosine, phosphoserine, phosphothreonine.
  • TCRs that have been modified to enhance their anti-proteolytic properties or to optimize solubility properties.
  • the TCR, TCR complexes of the invention or TCR transfected T cells of the invention can be provided in a pharmaceutical composition together with a pharmaceutically acceptable carrier.
  • the TCR, multivalent TCR complex or cell of the invention is typically provided as part of a sterile pharmaceutical composition, which typically comprises a pharmaceutically acceptable carrier.
  • the pharmaceutical composition can be in any suitable form (depending on the method desired for administration to a patient). It can be provided in unit dosage form, usually in a sealed container, and can be provided as part of a kit. Such kits (but not required) include instructions for use. It can include a plurality of said unit dosage forms.
  • the TCRs of the invention may be used alone or in combination or in combination with other therapeutic agents (e.g., formulated in the same pharmaceutical composition).
  • the pharmaceutical composition may also contain a pharmaceutically acceptable carrier.
  • pharmaceutically acceptable carrier refers to a carrier for the administration of a therapeutic agent.
  • pharmaceutical carriers which do not themselves induce the production of antibodies harmful to the individual receiving the composition and which are not excessively toxic after administration. These vectors are well known to those of ordinary skill in the art. A full discussion of pharmaceutically acceptable excipients can be found in Remington's Pharmaceutical Sciences (Mack Pub. Co., N. J. 1991).
  • Such carriers include, but are not limited to, saline, buffer, dextrose, water, glycerol, ethanol, adjuvants, and combinations thereof.
  • the pharmaceutically acceptable carrier in the therapeutic composition may contain a liquid such as water, saline, glycerol and ethanol.
  • auxiliary substances such as wetting or emulsifying agents, pH buffering substances and the like may also be present in these carriers.
  • the therapeutic compositions can be formulated as injectables, such as liquid solutions or suspensions; solid forms such as liquid carriers, which may be formulated in solution or suspension prior to injection.
  • composition of the invention can be administered by conventional routes including, but not limited to, intraocular, intramuscular, intravenous, subcutaneous, intradermal, or topical administration, preferably gastrointestinal.
  • External includes subcutaneous, intramuscular or intravenous.
  • the subject to be prevented or treated may be an animal; especially a human.
  • a pharmaceutical composition of various dosage forms may be employed depending on the use.
  • an injection, an oral preparation, or the like can be exemplified.
  • compositions can be formulated by mixing, diluting or dissolving according to conventional methods, and occasionally adding suitable pharmaceutical additives such as excipients, disintegrating agents, binders, lubricants, diluents, buffers, isotonicity Isotonicities, preservatives, wetting agents, emulsifiers, dispersing agents, stabilizers and solubilizers, and the formulation process can be carried out in a customary manner depending on the dosage form.
  • suitable pharmaceutical additives such as excipients, disintegrating agents, binders, lubricants, diluents, buffers, isotonicity Isotonicities, preservatives, wetting agents, emulsifiers, dispersing agents, stabilizers and solubilizers, and the formulation process can be carried out in a customary manner depending on the dosage form.
  • compositions of the invention may also be administered in the form of sustained release agents.
  • the TCR of the present invention can be incorporated into a pill or microcapsule in which the sustained release polymer is used as a carrier, and then the pill or microcapsule is surgically implanted into the tissue to be treated.
  • the sustained-release polymer an ethylene-vinyl acetate copolymer, polyhydrometaacrylate, polyacrylamide, polyvinylpyrrolidine can be exemplified.
  • a ketone, a methyl cellulose, a lactic acid polymer, a lactic acid-glycolic acid copolymer or the like is preferably exemplified by a biodegradable polymer such as a lactic acid polymer and a lactic acid-glycolic acid copolymer.
  • the TCR or TCR complex of the present invention as an active ingredient or the cell presenting the TCR of the present invention may be based on the body weight, age, sex, and degree of symptoms of each patient to be treated. And reasonable to determine, and ultimately the doctor determines the reasonable amount.
  • the present invention screens for a TCR having high affinity for the ILSLELMKL-HLA A0201 complex.
  • the affinity and/or binding half-life of the TCR of the present invention to the ILSLELMKL-HLA A0201 complex is at least 2-fold greater than that of the wild-type TCR.
  • the affinity and/or binding half-life of the high affinity TCR of the present invention to the ILSLELMKL-HLA A0201 complex can reach 10 3 -10 6 times that of the wild type TCR.
  • E. coli DH5 ⁇ is purchased from Tiangen, E. coli BL21 (DE3) and purchased from Tiangen, E. coli Tuner (DE3).
  • plasmid pET28a was purchased from Novagen.
  • the present invention utilizes a method of site-directed mutagenesis, according to the patent document WO2014/206304, to construct a stable single-chain TCR molecule composed of a flexible short peptide linked to a TCR ⁇ and a ⁇ -chain variable domain, the amino acid and the DNA thereof.
  • the sequences are SEQ ID NO: 1 and SEQ ID NO: 2, respectively, as shown in Figures 1a and 1b.
  • the single-chain TCR molecule was used as a template for screening high affinity TCR molecules.
  • amino acid sequences of the alpha variable domain (SEQ ID NO: 3) and the beta variable domain (SEQ ID NO: 4) of the template strand are shown in Figures 2a and 2b; the amino acid sequence of the flexible short linker is SEQ ID NO: 5, as shown in Figure 3.
  • the target gene carrying the template strand was digested with NcoI and NotI, and ligated with the pET28a vector digested with NcoI and NotI.
  • the ligation product was transformed into E. coli DH5 ⁇ , coated with kanamycin-containing LB plate, inverted culture at 37 ° C overnight, and the positive clones were picked for PCR screening.
  • the positive recombinants were sequenced to determine the correct sequence and the recombinant plasmid was extracted.
  • E. coli BL21 (DE3) for expression.
  • Example 2 Expression, renaturation and purification of single-chain TCR constructed in Example 1
  • the BL21(DE 3) colonies containing the recombinant plasmid pET28a-template strand prepared in Example 1 were all inoculated into LB medium containing kanamycin, and cultured at 37 ° C until the OD 600 was 0.6-0.8, and IPTG was added to the end. The concentration was 0.5 mM, and incubation was continued for 4 h at 37 °C.
  • the cell pellet was harvested by centrifugation at 5000 rpm for 15 min, the cell pellet was lysed with Bugbuster Master Mix (Merck), and the inclusion bodies were recovered by centrifugation at 6000 rpm for 15 min, and then washed with Bugbuster (Merck) to remove cell debris and membrane fraction, centrifuged at 6000 rpm for 15 min, and collected for inclusion. body.
  • the inclusion body was dissolved in a buffer (20 mM Tris-HCl pH 8.0, 8 M urea), and the insoluble matter was removed by high-speed centrifugation. The supernatant was fractionated by the BCA method, and then stored at -80 ° C until use.
  • the reconstituted solution was placed in a cellulose membrane dialysis bag with a cut-off amount of 4 kDa, and the dialysis bag was placed in 1 L of pre-cooled water and slowly stirred at 4 ° C overnight. After 17 hours, the dialysate was changed to 1 L of pre-cooled buffer (20 mM Tris-HCl pH 8.0), dialysis was continued for 8 h at 4 ° C, and the dialysate was replaced with the same fresh buffer to continue dialysis overnight.
  • pre-cooled buffer 20 mM Tris-HCl pH 8.0
  • the sample was filtered through a 0.45 ⁇ m filter, and the protein was purified by vacuum degassing through an anion exchange column (HiTrap Q HP, GE Healthcare) in a linear gradient of 0-mM NaCl prepared with 20 mM Tris-HCl pH 8.0.
  • the collected fractions were subjected to SDS-PAGE analysis, and the fractions containing the single-chain TCR were concentrated and further purified by a gel filtration column (Superdex 75 10/300, GE Healthcare), and the target components were also subjected to SDS-PAGE analysis.
  • the eluted fraction for BIAcore analysis was further tested for purity using gel filtration.
  • the conditions were as follows: column Agilent Bio SEC-3 (300A, ⁇ 7.8 ⁇ 300 mm), mobile phase 150 mM phosphate buffer, flow rate 0.5 mL/min, column temperature 25 ° C, UV detection wavelength 214 nm.
  • the binding activity of the TCR molecule to the ILSLELMKL-HLA A0201 complex was detected using a BIAcore T200 real-time assay system.
  • the anti-streptavidin antibody (GenScript) was added to a coupling buffer (10 mM sodium acetate buffer, pH 4.77), and then the antibody was passed through a CM5 chip previously activated with EDC and NHS to immobilize the antibody on the surface of the chip. Finally, the unreacted activated surface was blocked with a solution of ethanolamine in hydrochloric acid to complete the coupling process at a coupling level of about 15,000 RU.
  • a low concentration of streptavidin is passed over the surface of the coated antibody chip, then the ILSLELMKL-HLA A0201 complex is flowed through the detection channel, the other channel is used as a reference channel, and 0.05 mM biotin is then added at 10 ⁇ L/min.
  • the flow rate was passed through the chip for 2 min, blocking the remaining binding sites of streptavidin.
  • the affinity was determined by single-cycle kinetic analysis.
  • TCR was diluted to several different concentrations with HEPES-EP buffer (10 mM HEPES, 150 mM NaCl, 3 mM EDTA, 0.005% P20, pH 7.4) at a flow rate of 30 ⁇ L/min.
  • the bonding time of each injection is 120s, and let it dissociate for 600s after the last injection.
  • the chip was regenerated with 10 mM Gly-HCl, pH 1.75, after each round of assay.
  • Kinetic parameters were calculated using BIAcore Evaluation software.
  • E. coli bacterial solution inducing expression of heavy or light chain 100 ml of E. coli bacterial solution inducing expression of heavy or light chain was collected, and the cells were washed once with 8000 g of PBS at 10 ° C for 10 min, and then resuspended by vigorous shaking with 5 ml of BugBuster Master Mix Extraction Reagents (Merck). Incubate for 20 min at room temperature, then centrifuge at 6000 g for 15 min at 4 ° C, discard the supernatant, and collect inclusion bodies.
  • the above-mentioned inclusion weight was suspended in 5 ml BugBuster Master Mix, and incubated at room temperature for 5 min; 30 ml of BugBuster diluted 10 times, mixed, centrifuged at 6000 g for 15 min at 4 ° C; the supernatant was discarded, and 30 ml of BugBuster resuspended inclusion body was diluted 10 times.
  • the synthesized short peptide ILSLELMKL (Beijing Saibaisheng Gene Technology Co., Ltd.) was dissolved in DMSO to a concentration of 20 mg/ml.
  • the inclusion bodies of the light and heavy chains were dissolved with 8 M urea, 20 mM Tris pH 8.0, 10 mM DTT, and further denatured by adding 3 M guanidine hydrochloride, 10 mM sodium acetate, 10 mM EDTA before renaturation.
  • the ILSLELMKL peptide was added to the refolding buffer (0.4 M L-arginine, 100 mM Tris pH 8.3, 2 mM EDTA, 0.5 mM oxidized glutathione, 5 mM reduced glutathione, at 25 mg/L (final concentration), 0.2 mM PMSF, cooled to 4 ° C), then add 20 mg / L light chain and 90 mg / L heavy chain (final concentration, heavy chain added three times, 8h / time), renaturation at 4 ° C for at least 3 days By the time of completion, SDS-PAGE can be used to detect renaturation.
  • the refolding buffer 0.4 M L-arginine, 100 mM Tris pH 8.3, 2 mM EDTA, 0.5 mM oxidized glutathione, 5 mM reduced glutathione, at 25 mg/L (final concentration), 0.2 mM PMSF, cooled to 4 ° C
  • the renaturation buffer was replaced with 10 volumes of 20 mM Tris pH 8.0 for dialysis, and at least two buffers were exchanged to substantially reduce the ionic strength of the solution.
  • the protein solution was filtered through a 0.45 ⁇ m cellulose acetate filter and then loaded onto a HiTrap Q HP (GE General Electric Company) anion exchange column (5 ml bed volume).
  • the protein was eluted using a linear gradient of 0-400 mM NaCl prepared by an Akta Purifier (GE General Electric Company), 20 mM Tris pH 8.0, pMHC was eluted at approximately 250 mM NaCl, peak fractions were collected, and purity was determined by SDS-PAGE.
  • the purified pMHC molecule was concentrated using a Millipore ultrafiltration tube while the buffer was replaced with 20 mM Tris pH 8.0, followed by biotinylation reagent 0.05M Bicine pH 8.3, 10 mM ATP, 10 mM MgOAc, 50 ⁇ M D-Biotin, 100 ⁇ g/ml BirA
  • the enzyme (GST-BirA) was incubated overnight at room temperature and SDS-PAGE was used to determine if biotinylation was complete.
  • the biotinylated labeled pMHC molecule was concentrated to 1 ml using a Millipore ultrafiltration tube, biotinylated pMHC was purified by gel filtration chromatography, and HiPrep was pre-equilibrated with filtered PBS using an Akta Purifier (GE General Electric Company).
  • Akta Purifier GE General Electric Company
  • a TM 16/60 S200 HR column (GE General Electric Company) was loaded with 1 ml of concentrated biotinylated pMHC molecules and then eluted with PBS at a flow rate of 1 ml/min.
  • the biotinylated pMHC molecule appeared as a single peak elution at about 55 ml.
  • the protein-containing fractions were pooled, concentrated using a Millipore ultrafiltration tube, protein concentration was determined by BCA method (Thermo), and biotinylated pMHC molecules were dispensed at -80 °C by adding protease inhibitor cocktail (Roche).
  • Phage display technology is a means of generating TCR high affinity variant libraries to screen for high affinity variants.
  • the TCR phage display and screening method described by Li et al. ((2005) Nature Biotech 23(3): 349-354) was applied to the single-chain TCR template of Example 1.
  • a library of high affinity TCRs was created and panned by mutating the CDR regions of the template strand.
  • Those skilled in the art can obtain the library construction and screening method by reading the above documents. That is by using one or more codon changes that are required Primers and plasmids containing relevant DNA as templates are implemented. After several rounds of panning, the phage library specifically binds to the corresponding antigen, picks up the monoclonal and performs sequence analysis.
  • the BIAcore method of Example 3 was used to analyze the interaction of the TCR molecule with the ILSLELMKL-HLA A0201 complex, and the high affinity TCR with affinity and/or binding half-life of at least 2 times that of the wild-type TCR was screened, ie, the selected high solution binding affinity TCR ILSLELMKL-HLA A0201 complex dissociation equilibrium constant K D or less of wild-type TCR binding solution ILSLELMKL-HLA A0201 complex equilibrium constant K D from one-half, the results shown in table 2 below.
  • the alpha chain variable domains of these high affinity TCR mutants are mutated at one or more of the following amino acids: 28R, 29V, 30S, 32S, 50I, 52S, 53N, 55D, 94S, 96Y, 97A and 98L and/or the numbering of the ⁇ -chain variable domains of these high-affinity TCR mutants at one or more of the following positions using the numbering shown in SEQ ID NO:37 Mutations 27G, 28T, 29S, 30N, 31P, 32N, 53I, 54G, 92A, 93W and 95V occurred.
  • the alpha chain variable domains of these high affinity TCRs comprise one or more amino acid residues 28I, 28K, or 28M selected from the group consisting of 29Y or 29L; 30N ; 32A; 50L; 52R; 53G; 55S or 55T; 94D; 96I; 97H, 97I, 97V or 97L; 98M, 98I or 98F; and/or using the number shown in SEQ ID NO: 37, these high affinity TCR
  • the ⁇ chain variable domain comprises one or more amino acid residues 27P or 27L selected from the group consisting of 28H, 28S, 28R or 28D; 29N, 29Y or 29D; 30P, 30T, 30I or 30L; 31R; 32L, 32A or 32I; 53V; 54R; 92S; 93Y; 95L.
  • the CDRs of the ⁇ and ⁇ chain variable domains of the high-affinity single-stranded TCRs screened in Example 4 were transferred to the corresponding sites of the variable domains of ⁇ heterodimeric TCR, respectively, and detected by BIAcore. Affinity of the ILSLELMKL-HLA A0201 complex.
  • the introduction of high affinity mutation points in the above CDR regions employs a method of site-directed mutagenesis well known to those skilled in the art. Since the CDR regions of the TCR variable region determine their affinity to the pMHC complex, one skilled in the art can predict that a high affinity alpha beta heterodimeric TCR can be obtained upon introduction of the above-described selected CDR region mutations.
  • the alpha chain and beta chain variable domain amino acid sequences of the above wild type TCR are shown in Figures 6a (SEQ ID NO: 36) and 6b (SEQ ID NO: 37), respectively.
  • the ⁇ heterodimeric TCR may be constant in the ⁇ and ⁇ chains.
  • a cysteine residue was introduced into the region to form a TCR of an artificial interchain disulfide bond.
  • the amino acid sequences of the TCR ⁇ and ⁇ chain after introducing a cysteine residue in this example are shown in Figure 7a (SEQ ID). NO: 38) and 7b (SEQ ID NO: 39), the introduced cysteine residues are indicated by bold letters.
  • the extracellular sequence genes of the TCR ⁇ and ⁇ chains to be expressed are synthesized and inserted into the expression vector by standard methods described in the Molecular Cloning a Laboratory Manual (3rd edition, Sambrook and Russell).
  • pET28a+ Novagene
  • the upstream and downstream cloning sites are NcoI and NotI, respectively.
  • Mutations in the CDR regions are introduced by overlapping PCR (overlap PCR) well known to those skilled in the art. The insert was sequenced to confirm that it was correct.
  • TCR ⁇ and ⁇ chain were transformed into expression plasmid BL21(DE3) by chemical transformation, respectively, and the bacteria were grown in LB medium.
  • the resulting inclusion bodies were extracted by BugBuster Mix (Novagene) and washed repeatedly with BugBuster solution.
  • the inclusion bodies were finally dissolved in 6 M guanidine hydrochloride, 10 mM dithiothreitol (DTT), 10 mM ethylenediaminetetraacetic acid (EDTA). ), in 20 mM Tris (pH 8.1).
  • the dissolved TCR ⁇ and ⁇ chains are rapidly mixed in 5M urea at a mass ratio of 1:1, 0.4M fine A solution of 20 mM Tris (pH 8.1), 3.7 mM cystamine, 6.6 mM ⁇ -mercapoethylamine (4 ° C) at a final concentration of 60 mg/mL. After mixing, the solution was dialyzed against 10 volumes of deionized water (4 ° C), and after 12 hours, deionized water was exchanged for buffer (20 mM Tris, pH 8.0) and dialysis was continued at 4 ° C for 12 hours.
  • the solution after completion of dialysis was filtered through a 0.45 ⁇ M filter, and then purified by an anion exchange column (HiTrap Q HP, 5 ml, GE Healthcare).
  • the TCR containing the refolding successful alpha and beta dimers was confirmed by SDS-PAGE gel.
  • the TCR was then further purified by gel filtration chromatography (HiPrep 16/60, Sephacryl S-100 HR, GE Healthcare).
  • the purified TCR purity was determined by SDS-PAGE to be greater than 90%, and the concentration was determined by the BCA method.
  • Example 7 Expression, renaturation and purification of fusions of anti-CD3 antibodies with high affinity single chain TCR
  • the high affinity single-chain TCR molecule of the present invention is fused with a single-stranded molecule (scFv) of an anti-CD3 antibody to construct a fusion molecule.
  • scFv single-stranded molecule
  • primers were designed, the anti-CD3 antibody and the gene of the high-affinity single-chain TCR molecule were ligated, and the intermediate linker was designed as GGGGS, and the gene fragment of the fusion molecule was brought on. Restriction enzyme sites NcoI and NotI.
  • the PCR amplification product was digested with NcoI and NotI and ligated with the pET28a vector digested with NcoI and NotI. The ligation product was transformed into E.
  • coli DH5 ⁇ competent cells coated with kanamycin-containing LB plates, and cultured overnight at 37 ° C. Positive clones were picked for PCR screening, positive recombinants were sequenced, and the sequence was determined to be correct. The recombinant plasmid was transformed into E. coli BL21 (DE3) competent cells for expression.
  • the expression plasmid containing the gene of interest was transformed into Escherichia coli strain BL21 (DE3), and LB plate (kanamycin 50 ⁇ g/ml) was applied and cultured at 37 ° C overnight. On the next day, the clones were inoculated into 10 ml of LB liquid medium (kanamycin 50 ⁇ g/ml) for 2-3 h, and inoculated into 1 L of LB medium (kanamycin 50 ⁇ g/ml) at a volume ratio of 1:100. The culture was carried out until the OD 600 was 0.5-0.8, and then the expression of the protein of interest was induced using IPTG at a final concentration of 0.5 mM.
  • the cells were harvested by centrifugation at 6000 rpm for 10 min.
  • the cells were washed once in PBS buffer, and the cells were dispensed, and the cells corresponding to 200 ml of the bacterial culture were lysed with 5 ml of BugBuster Master Mix (Novagen), and the inclusion bodies were collected by centrifugation at 6000 g for 15 minutes.
  • a detergent wash was then performed 4 times to remove cell debris and membrane components.
  • the inclusion bodies are then washed with a buffer such as PBS to remove detergent and salt.
  • the inclusion bodies were dissolved in a Tris buffer solution containing 8 M urea, and the inclusion body concentration was measured, and the package was divided and stored at -80 ° C for cryopreservation.
  • inclusion bodies were taken out from the -80 ° C ultra-low temperature freezer and thawed, and dithiothreitol (DTT) was added to a final concentration of 10 mM, and incubated at 37 ° C for 30 minutes to 1 hour to ensure complete opening of the disulfide bond. Then, the inclusion body sample solution was separately dropped into 200 ml of 4 ° C pre-cooled refolding buffer (100 mM Tris pH 8.1, 400 mM L-arginine, 2 mM EDTA, 5 M urea, 6.5 mM ⁇ -mercapthoethylamine, 1.87 mM Cystamine), 4 ° C Stir slowly for about 30 minutes.
  • DTT dithiothreitol
  • the renaturation solution was dialyzed against 8 volumes of pre-cooled H 2 O for 16-20 hours. It was further dialyzed twice with 8 volumes of 10 mM Tris pH 8.0, and dialysis was continued at 4 ° C for about 8 hours. After dialysis, the sample was filtered and subjected to the following purification.
  • the dialyzed heavy fold (10 mM Tris pH 8.0) was eluted with a gradient of 0-600 mM NaCl using an POROS HQ/20 anion exchange chromatography prepacked column (Applied Biosystems) on an AKTA Purifier (GE Healthcare). Each component was analyzed by Coomassie-stained SDS-PAGE, then merge.
  • the first step of the purified sample solution was concentrated for purification in this step, and the fusion protein was purified by Superdex 75 10/300 GL gel filtration chromatography prepacked column (GE Healthcare) pre-equilibrated in PBS buffer, Coomassie Brilliant Blue The fractions of the peaks were analyzed by stained SDS-PAGE and then combined.
  • Example 8 Expression, renaturation and purification of fusions of anti-CD3 antibodies with high affinity ⁇ heterodimeric TCRs
  • a fusion molecule is prepared by fusing an anti-CD3 single-chain antibody (scFv) with an ⁇ heterodimeric TCR.
  • the anti-CD3 scFv is fused to the ⁇ chain of the TCR, and the TCR ⁇ chain may comprise the ⁇ chain variable domain of any of the above high affinity ⁇ heterodimeric TCRs, and the TCR ⁇ chain of the fusion molecule may comprise any of the above high affinity
  • the target gene carrying the ⁇ chain of the ⁇ heterodimeric TCR was digested with NcoI and NotI, and ligated with the pET28a vector digested with NcoI and NotI.
  • the ligation product was transformed into E. coli DH5 ⁇ , plated on LB plate containing kanamycin, and cultured overnight at 37 ° C.
  • the positive clones were picked for PCR screening, and the positive recombinants were sequenced to determine the correct sequence and the recombinant plasmid was extracted. Transformed to E. coli Tuner (DE3) for expression.
  • the primers were designed to ligate the anti-CD3 scFv and the high-affinity heterodimeric TCR ⁇ chain gene by overlapping PCR, the intermediate linker was GGGGS, and the anti-CD3 scFv was The gene fragment of the fusion protein of the high affinity heterodimeric TCR ⁇ chain carries the restriction enzyme sites NcoI (CCATGG) and NotI (GCGGCCGC).
  • the PCR amplification product was digested with NcoI and NotI and ligated with the pET28a vector digested with NcoI and NotI.
  • the ligation product was transformed into E. coli DH5 ⁇ competent cells, coated with kanamycin-containing LB plates, and cultured overnight at 37 ° C. Positive clones were picked for PCR screening, positive recombinants were sequenced, and the sequence was determined to be correct.
  • the recombinant plasmid was transformed into E. coli Tuner (DE3) competent cells for expression.
  • the expression plasmids were separately transformed into E. coli Tuner (DE3) competent cells, and LB plates (kanamycin 50 ⁇ g/mL) were applied and cultured at 37 ° C overnight. On the next day, the clones were inoculated into 10 mL LB liquid medium (kanamycin 50 ⁇ g/mL) for 2-3 h, inoculated into 1 L LB medium at a volume ratio of 1:100, and the culture was continued until the OD600 was 0.5-0.8. The final concentration of 1 mM IPTG induced the expression of the protein of interest. After 4 hours of induction, the cells were harvested by centrifugation at 6000 rpm for 10 min.
  • the cells were washed once in PBS buffer, and the cells were dispensed, and the cells corresponding to 200 mL of the bacterial culture were lysed with 5 mL of BugBuster Master Mix (Merck), and the inclusion bodies were collected by centrifugation at 6000 g for 15 minutes. A detergent wash was then performed 4 times to remove cell debris and membrane components. The inclusion bodies are then washed with a buffer such as PBS to remove detergent and salt.
  • a buffer such as PBS to remove detergent and salt.
  • inclusion bodies were dissolved in a buffer solution containing 6 M guanidine hydrochloride, 10 mM dithiothreitol (DTT), 10 mM ethylenediaminetetraacetic acid (EDTA), 20 mM Tris, pH 8.1, and the inclusion body concentration was determined and dispensed. It was then stored frozen at -80 °C.
  • the dissolved TCR ⁇ chain and anti-CD3(scFv)- ⁇ chain were rapidly mixed in a mass ratio of 2:5 to 5M urea (urea), 0.4M L-arginine (L-arginine), 20mM Tris pH 8.1, 3.7 mM Cystamine, 6.6 mM ⁇ -mercapoethylamine (4 ° C), final concentration ⁇ chain and anti-CD3 (scFv)- ⁇ chain were 0.1 mg/mL, 0.25 mg/mL, respectively.
  • the solution was dialyzed against 10 volumes of deionized water (4 ° C), and after 12 hours, deionized water was exchanged for buffer (10 mM Tris, pH 8.0) and dialysis was continued at 4 ° C for 12 hours.
  • the solution after completion of dialysis was filtered through a 0.45 ⁇ M filter, and then purified by an anion exchange column (HiTrap Q HP 5 ml, GE healthcare).
  • the TCR of the eluted peak containing the reconstituted TCR alpha chain and the anti-CD3 (scFv)-beta chain dimer was confirmed by SDS-PAGE gel.
  • the TCR fusion molecule was then further purified by size exclusion chromatography (S-100 16/60, GE healthcare) and anion exchange column (HiTrap Q HP 5 ml, GE healthcare). The purity of the purified TCR fusion molecule was determined by SDS-PAGE to be greater than 90%, and the concentration was determined by the BCA method.
  • This example demonstrates that fusions of anti-CD3 antibodies with high affinity single chain TCRs are capable of mediating effector cell recognition and activation of RHAMM antigen positive cancer cells.
  • the fusion of the anti-CD3 antibody prepared in Example 7 with the high-affinity single-chain TCR was tested for its function and specificity in the cells by ELISPOT assay.
  • Methods for detecting cellular function using ELISPOT assays are well known to those skilled in the art.
  • the effector cells used in the IFN- ⁇ ELISPOT assay of this example were CD8+ T cells isolated from the blood of healthy volunteers, and the target cell lines were antigenic (RHAMM)-positive IM9 (674) and Mel 526 (390) cells.
  • the group was HLA-negative (A2-) SK-BR-3 cells.
  • ELISPOT tablet On day 0 of the experiment, ELISPOT plate ethanol was coated with activation at 4 ° C overnight. On the first day of the experiment, the coating solution was removed, washed and blocked, and incubated at room temperature for two hours to remove the blocking solution. The components of the assay were added to the ELISPOT plate in the following order: medium adjusted CD8+ T cells to 8 ⁇ 10 4 cells/ml. The medium was adjusted to 2 ⁇ 105 cells/ml for each target cell line, and the medium was diluted to a concentration of 0.04 ⁇ M, and serially diluted by 10 times, for a total of 6 concentration gradients.
  • Example 10 Cellular function and specificity of fusion of anti-CD3 antibody with high affinity ⁇ heterodimeric TCR
  • This example demonstrates that fusions of an anti-CD3 antibody with a high affinity alpha beta heterodimeric TCR can mediate effector cell recognition of RHAMM antigen positive cancer cell recognition and activation functions.
  • the fusion of the anti-CD3 antibody prepared in Example 8 and the high affinity ⁇ heterodimeric TCR was tested for its function and specificity in the cells by ELISPOT assay.
  • Methods for detecting cellular function using ELISPOT assays are well known to those skilled in the art.
  • the effector cells used in the IFN- ⁇ ELISPOT assay of this example are CD8+ T cells isolated from the blood of healthy volunteers, and the target cell line is an antigen. (RHAMM) positive IM9 (674) and Mel 526 (390) cells, and control group were HLA negative (A2-) SK-BR-3 cells.
  • ELISPOT tablet On day 0 of the experiment, ELISPOT plate ethanol was coated with activation at 4 ° C overnight. On the first day of the experiment, the coating solution was removed, washed and blocked, and incubated at room temperature for two hours to remove the blocking solution. The components of the assay were added to the ELISPOT plate in the following order: medium adjusted CD8+ T cells to 8 ⁇ 10 4 cells/ml. The medium was adjusted to 2 ⁇ 105 cells/ml for each target cell line, and the medium was diluted to a concentration of 0.04 ⁇ M, and serially diluted by 10 times, for a total of 6 concentration gradients.
  • the anti-CD3 antibody and the high affinity ⁇ heterodimeric TCR fusion mediated effector cells were positive for antigen (RHAMM).
  • the IM9 and Mel526 cell lines have a specific response.

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Abstract

La présente invention concerne récepteur de lymphocyte T (TCR) ayant les caractéristiques de liaison au complexe ILSLELMKL-HLA A0201. L'affinité du TCR pour la liaison au complexe ILSLELMKL-HLA A0201 est au moins deux fois l'affinité d'un TCR sauvage pour la liaison au complexe ILSLELMKL-HLA A0201. L'invention concerne en outre une molécule de fusion de TCR et d'un agent thérapeutique. Le TCR peut être utilisé indépendamment ou en combinaison avec un agent thérapeutique pour présenter de façon ciblée le complexe ILSLELMKL-HLA A0201 à une cellule tumorale.
PCT/CN2016/098248 2015-09-09 2016-09-06 Récepteur de lymphocyte t ayant une affinité élevée de ciblage de polypeptide à chaîne courte d'antigène rhamm WO2017041704A1 (fr)

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WO2022262842A1 (fr) * 2021-06-18 2022-12-22 香雪生命科学技术（广东）有限公司 Récepteur de lymphocytes t à haute affinité pour antigène afp

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CN104684926A (zh) * 2012-07-27 2015-06-03 伊利诺伊州大学理事会 工程化t细胞受体

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CN104684926A (zh) * 2012-07-27 2015-06-03 伊利诺伊州大学理事会 工程化t细胞受体

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GREINER J; ET AL: "Identification and Characterization of Epitopes of the Receptor for Hyaluronic Acid-Mediated Motility (RHAMM/ CD 168) Recognized by CD 8+ T Cells of HLA-A2-Positive Patients with Acute Myeloid Leukemia", BLOOD, vol. 106, no. 3, 12 April 2005 (2005-04-12), pages 938 - 945, XP055329472 *
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WO2022262842A1 (fr) * 2021-06-18 2022-12-22 香雪生命科学技术（广东）有限公司 Récepteur de lymphocytes t à haute affinité pour antigène afp

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