WO2022039547A1 - 감마 불변부위(cγ1)와 엡실론 불변부위(cε2-4)가 융합된 중쇄와 경쇄의 불변부위로 이루어진 항체 단편 및 이의 용도 - Google Patents
감마 불변부위(cγ1)와 엡실론 불변부위(cε2-4)가 융합된 중쇄와 경쇄의 불변부위로 이루어진 항체 단편 및 이의 용도 Download PDFInfo
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- C—CHEMISTRY; METALLURGY
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- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/001—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof by chemical synthesis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6854—Immunoglobulins
- G01N33/6857—Antibody fragments
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/52—Constant or Fc region; Isotype
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
Definitions
- the present invention relates to an antibody fragment composed only of an antibody constant region, and more particularly, to an antibody fragment composed only of the heavy chain (CH) and light chain (CL) constant regions without the variable region of the antibody.
- an antibody fragment named IgCw- ⁇ 1 ⁇ 2-4/ ⁇ , abbreviated as IgCw- ⁇
- a nucleic acid encoding the same a kit comprising the same, and uses thereof.
- a reference antibody that is, a control antibody that does not bind to the target molecule (antigen) of the antibody to evaluate the efficacy.
- a reference antibody can be isolated from a polyclonal antibody or produced from the culture of cells transfected with expression constructs encoding the heavy and light chain regions of the antibody.
- the reference antibody does not bind to the target molecule to which the antibody binds to evaluate the efficacy, a noise positive signal is generated because the reference antibody also has a variable region involved in binding to any antigen.
- the possibility of cross-reactivity, in particular, the possibility of an off-target effect by reaction with other antigens cannot be completely excluded.
- immunoglobulin E is an antibody present in a very low concentration in the blood. Measuring the concentration of IgE in the blood is important for diagnosing IgE-related immune diseases and tracking the therapeutic effect. For quantification of IgE, a reference IgE protein is absolutely necessary. In addition, there is a need for IgE protein in various qualitative immunological experiments.
- IgE proteins are: 1) Monoclonal IgE purified from the blood of patients with high blood IgE concentrations (eg, patients with IgE myeloma) (eg Abcam, Athens Research & Technology, MyBioSource, Fitzgerald Industries International, Molecular) innovations, and products of Merck Millipore), 2) monoclonal IgE purified from a culture medium of hybridoma cells made by fusion of myeloma cells with B cells derived from healthy people, 3) cell line obtained by transfecting the IgE gene monoclonal IgE purified from the culture medium of
- IgE antibodies are more than 100 times more expensive than IgG, and contain variable regions (VH and VL).
- IgE 3rd International Reference Preparation
- coded 11/234 used for the quantification of total IgE in blood, and the concentration of IgE in the blood is high.
- Plasma (or serum) of patients from various countries is collected and put into each ampoule and freeze-dried. It contains blood components and is considered a biohazard and requires caution when used in a laboratory.
- WHO IRP 11/234 is polyclonal IgE. , there is a problem that the possibility of non-specific binding to an unknown antigen cannot be excluded.
- the present inventors tried to develop a new type of antibody fragment that can replace the IgE reference antibody while avoiding the disadvantages of the previously known IgE reference antibody.
- Fc ⁇ R Fc apsilon receptor
- a molecule consisting only of constant regions and not having variable regions, in particular, a heavy chain (C ⁇ 1-) in which a gamma constant region (C ⁇ 1)-hinge and an epsilon constant region (C ⁇ 2-4) are fused. hinge-C ⁇ 2-4) and an antibody fragment (IgCw- ⁇ ) composed of the light chain kappa constant region (C K ) was developed. It was confirmed that this IgCw- ⁇ molecule can be used as an IgE substitute in an IgE concentration measurement experiment and immunological studies by Fc ⁇ R-IgE interaction, and can inhibit IgE-mediated hypersensitivity disease, and completed the present invention. .
- the present invention provides a heavy chain constant region fragment of an IgG antibody and a heavy chain constant region fragment of an IgE antibody; And it provides an antibody fragment comprising a light chain constant region fragment linked to the heavy chain constant region fragment.
- the present invention also provides a nucleic acid encoding the antibody fragment.
- the present invention also provides a kit comprising the antibody fragment.
- the present invention also provides a composition for evaluating antibody efficacy comprising the antibody fragment.
- the present invention also provides a composition for measuring an antibody concentration comprising the antibody fragment.
- the present invention also provides a composition for inhibiting allergic reaction comprising the antibody fragment.
- the present invention also provides a composition for inhibiting IgE-mediated autoimmune reaction comprising the antibody fragment.
- IgCw- ⁇ 1 ⁇ 2-4/ ⁇ (simply IgCw- ⁇ ) protein structure.
- An antibody fragment (about 130 kDa) consisting of the human antibody C ⁇ 1-hinge region and C ⁇ 2-C ⁇ 3-C ⁇ 4 is shown.
- Figure 2 shows the results of analyzing the purification purity and integrity (integrity) of the purified antibody proteins.
- IgCw- ⁇ has a molecular weight of about 130 kDa as expected.
- A is the result of Coomassie staining after SDS-PAGE.
- B shows the size exclusion chromatography results.
- FIG. 3 is a binding analysis of IgCw- ⁇ and Fc ⁇ R. Flow cytometry results showing that IgCw- ⁇ antibody fragment protein can bind as well as control IgE to the high affinity human Fc ⁇ receptor (Fc ⁇ R1) expressed on the RBL-2H3-Fc ⁇ RI ⁇ cell surface is shown.
- IgCw- ⁇ shows the results of confirming the degranulation reaction by cross-linking of IgCw- ⁇ .
- IgCw- ⁇ was at a level similar to that of full-size IgE as a control. This is an experimental result showing that beta-hexosaminidase release (degranulation reaction) can be induced.
- A shows the experimental design, and B shows the experimental results.
- A is the experimental design
- B is the measurement result of beta-hexosaminidase release from RBL-2H3-Fc ⁇ RI ⁇ cells treated with 6C407 IgE and IgCw- ⁇ mixture
- C is 6C407 IgE to RBL-2H3-Fc ⁇ RI cells After the pre-treatment, the beta-hexosaminidase release degree from the cells by treatment with IgCw- ⁇ is shown.
- IgCw- ⁇ is a result showing IgCw- ⁇ as a reference molecule for quantification of human IgE antibody. This is an ELISA result showing that the IgCw- ⁇ protein can be used as a reference for IgE antibody quantification.
- A is a standard curve generated using 6C407 IgE, and B is a standard curve generated using IgCw- ⁇ .
- the antibody fragment IgCw- ⁇ which consists of the constant regions of the heavy and light chains fused with the gamma constant region (C ⁇ 1)-hinge and the epsilon constant region (C ⁇ 2-4), disulfide bonds between the constant regions are normally formed, and the expression level and The purification yield was also similar to that of control 6C407 IgE. As such, the fusion of the gamma constant region (C ⁇ 1) and the epsilon constant region (C ⁇ 2-4) allows the IgCw- ⁇ protein to have structural stability and high purification yield.
- IgCw- ⁇ is an antibody fragment consisting of two C ⁇ 1-hinge-C ⁇ 2-4 hybrid heavy chains and two C ⁇ light chains, and consists only of constant regions, and variable regions ) is a molecule that does not have
- the present invention provides a heavy chain constant region fragment of an IgG antibody and a heavy chain constant region fragment of an IgE antibody; And it relates to an antibody fragment comprising a light chain constant region fragment linked to the heavy chain constant region fragment.
- antibody fragment refers to a novel antibody format, including a heavy chain constant region fragment of an IgG antibody and a heavy chain constant region fragment of an IgE antibody without an antibody variable region; And the development of an antibody fragment comprising a light chain constant region fragment linked to the heavy chain constant region fragment, IgCw- ⁇ having such a new structure has a variety of advantages, it was identified that can be widely used in clinical fields such as antibody efficacy evaluation did
- An unfragmented antibody comprises two heavy chains and two light chains linked by disulfide bonds. Each single light chain is linked to one of the heavy chains by a disulfide bond.
- the antibody heavy chain portion consists of a variable domain (V H ) at the N-terminus followed by a number of constant domains (depending on the antibody class, 3 or 4 constant domains, C H 1 , C H 2 , C H 3 and C H 4 ).
- each light chain portion has a variable region (VL) at its N-terminus and a constant region (CL) at its other end (C-terminus), the constant region of the light chain aligned with the first constant region of the heavy chain (CH1),
- the light chain variable region (V L ) is aligned with the variable region (V H ) of the heavy chain.
- the constant region refers to the sum of domains of an antibody other than the variable region. Although constant regions are not directly involved in the binding of an antibody to its target antigen, they are involved in various effector functions in vivo.
- the heavy and light chain constant regions are used to include all those derived from IgA, IgD, IgE, IgG and IgM as well as IgY, IgW and IgNAR.
- the IgG is a subtype, and may include IgG1, IgG2, IgG3, and IgG4.
- the heavy chain constant region fragment of the IgG antibody may include C ⁇ 1.
- the heavy chain constant region fragment of the IgE antibody may include at least one selected from the group consisting of C ⁇ 2, C ⁇ 3 and C ⁇ 4.
- the antibody fragment according to the present invention comprises heavy chain constant region fragment C ⁇ 1 of an IgG antibody, heavy chain constant region fragments C ⁇ 2, C ⁇ 3 and C ⁇ 4 of an IgE antibody, and a heavy chain constant region fragment of an IgG antibody and heavy chain constant region fragment of an IgE antibody
- the site fragment may be linked by C ⁇ 1-C ⁇ 2-C ⁇ 3-C ⁇ 4 in an N-terminal to C-terminal direction.
- the heavy chain constant region fragment of the IgG antibody and the heavy chain constant region fragment of the IgE antibody may be linked through a hinge.
- the light chain constant region may include C ⁇ or C ⁇ .
- the light chain constant region fragment linked to the heavy chain constant region fragment may be bonded by, for example, a disulfide bond or a peptide linker.
- Recombinant antibody formats have frequently encountered difficulties due to low purification yields that can affect utility and cost effectiveness.
- the production yield of the antibody depends on the characteristics (amino acid sequence) of the heavy chain variable region (V H ) and the light chain variable region (V L ). Therefore, the production yield of a recombinant antibody can be quite variable depending on the amino acid sequence of the variable domain (V domain) even in a well-established manufacturing process.
- the antibody fragment consisting only of the antibody constant region according to the present invention can be produced in high yield.
- the present invention relates to a nucleic acid encoding the antibody fragment.
- Antibody fragments can be recombinantly produced by isolating the nucleic acid.
- the nucleic acid is isolated and inserted into a replicable vector for further cloning (amplification of the DNA) or further expression. Based on this, the present invention relates to a vector comprising the nucleic acid from another aspect.
- Nucleic acid has a meaning comprehensively encompassing DNA (gDNA and cDNA) and RNA molecules, and nucleotides, which are the basic building blocks of nucleic acids, include natural nucleotides as well as analogues in which sugar or base regions are modified. .
- the sequences of the nucleic acids encoding the heavy and light chain variable regions of the present invention may be modified. Such modifications include additions, deletions, or non-conservative or conservative substitutions of nucleotides.
- Vector components generally include, but are not limited to, one or more of the following: a signal sequence, an origin of replication, one or more marker genes, an enhancer element, a promoter, and a transcription termination sequence.
- the term "vector” refers to a means for expressing a target gene in a host cell, including a plasmid vector; cozmid vector; viral vectors such as bacteriophage vectors, adenoviral vectors, retroviral vectors and adeno-associated viral vectors, and the like.
- the nucleic acid encoding the antibody fragment is operably linked with a promoter.
- “Operably linked” refers to a functional association between a nucleic acid expression control sequence (eg, a promoter, signal sequence, or array of transcriptional regulator binding sites) and another nucleic acid sequence, whereby the control sequence is linked to the other nucleic acid. to regulate the transcription and/or translation of the sequence.
- a nucleic acid expression control sequence eg, a promoter, signal sequence, or array of transcriptional regulator binding sites
- a strong promoter capable of propagating transcription eg, tac promoter, lac promoter, lacUV5 promoter, lpp promoter, pL ⁇ promoter, pR ⁇ promoter, rac5 promoter, amp promoter, recA promoter, SP6 promoter, trp promoter and T7 promoter
- a ribosome binding site for initiation of translation e.g, lac promoter, lacUV5 promoter, lpp promoter, pL ⁇ promoter, pR ⁇ promoter, rac5 promoter, amp promoter, recA promoter, SP6 promoter, trp promoter and T7 promoter
- a promoter derived from the genome of a mammalian cell eg, a metallotionine promoter, a ⁇ -actin promoter, a human heglobin promoter, and a human muscle creatine promoter
- a mammalian cell eg, a metallotionine promoter, a ⁇ -actin promoter, a human heglobin promoter, and a human muscle creatine promoter
- Promoters derived from animal viruses e.g., adenovirus late promoter, vaccinia virus 7.5K promoter, SV40 promoter, cytomegalovirus (CMV) promoter, tk promoter of HSV, mouse mammary tumor virus (MMTV) promoter, LTR promoter of HIV , the promoter of Moloney virus, the promoter of Epstein Barr virus (EBV) and the promoter of Loose sarcoma virus (RSV)), and generally has a polyadenylation sequence as a transcription termination sequence.
- animal viruses e.g., adenovirus late promoter, vaccinia virus 7.5K promoter, SV40 promoter, cytomegalovirus (CMV) promoter, tk promoter of HSV, mouse mammary tumor virus (MMTV) promoter, LTR promoter of HIV , the promoter of Moloney virus, the promoter of Epstein Barr virus (EBV) and the promoter of Loose sarcom
- the vector may be fused with other sequences to facilitate purification of the antibody fragment expressed therefrom.
- the sequence to be fused includes, for example, glutathione S-transferase (Pharmacia, USA), maltose binding protein (NEB, USA), FLAG (IBI, USA) and 6x His (hexahistidine; Quiagen, USA).
- the vector contains an antibiotic resistance gene commonly used in the art as a selection marker, and for example, ampicillin, gentamicin, carbenicillin, chloramphenicol, streptomycin, kanamycin, geneticin, neomycin and tetracycline. There is a resistance gene.
- the present invention relates to a cell transformed with the above-mentioned vector.
- the cells used to produce the antibody fragments of the invention can be, but are not limited to, prokaryotic, yeast or higher eukaryotic cells.
- Bacillus genus strains such as Escherichia coli, Bacillus subtilis and Bacillus thuringiensis, Streptomyces, Pseudomonas (eg Pseudomonas putida), Proteus Prokaryotic host cells such as Proteus mirabilis and Staphylococcus (eg, Staphylocus carnosus) can be used.
- animal cells are of greatest interest, and examples of useful host cell lines include COS-7, BHK, CHO, CHOK1, DXB-11, DG-44, CHO/-DHFR, CV1, COS-7, HEK293, BHK, TM4, VERO, HELA, MDCK, BRL 3A, W138, Hep G2, SK-Hep, MMT, TRI, MRC 5, FS4, 3T3, RIN, A549, PC12, K562, PER.C6, SP2/0, NS-0 , U20S, or may be HT1080, but is not limited thereto.
- the present invention (a) culturing the cell; and (b) recovering the antibody fragment from the cultured cells.
- the cells may be cultured in various media. Among commercially available media, it can be used as a culture medium without limitation. All other essential supplements known to those skilled in the art may be included in appropriate concentrations. Culture conditions, such as temperature, pH, etc., are already in use with the host cells selected for expression, as will be apparent to those skilled in the art.
- the antibody fragment may be recovered, for example, by centrifugation or ultrafiltration to remove impurities, and the resultant product may be purified using, for example, affinity chromatography. Additional other purification techniques may be used, such as anion or cation exchange chromatography, hydrophobic interaction chromatography, hydroxylapatite chromatography, and the like.
- the present invention relates to a kit comprising an antibody fragment.
- the kit may include a container including the antibody fragment and a container including other reagents or samples.
- the kit is suitable for containing one or more containers, such as bottles and tubes, each container containing independent components for use in the method of the present invention.
- containers such as bottles and tubes
- each container containing independent components for use in the method of the present invention.
- one of ordinary skill in the art can readily dispense the required formulation in a container.
- the present invention relates to a composition for evaluating antibody efficacy comprising the antibody fragment.
- a reference (or irrelevant isotype control) antibody is commonly used as a negative control to distinguish a non-specific background signal from an antigen-specific antibody signal.
- existing reference antibodies may still give unwanted noise signals due to the as yet unknown cross-reactivity.
- the antibody fragment according to the present invention lacks antigen-binding ability and can exclude the possibility of unpredictable cross-reactivity, it can be a better reference antibody in many experimental environments and situations compared to irrelevant IgE controls.
- the present invention relates to a composition for measuring an antibody concentration comprising the antibody fragment.
- the antibody fragment according to the present invention can be used as a reference for measuring the concentration of immunoglobulin in a biological sample.
- the present invention relates to a composition for inhibiting allergic reaction comprising an antibody fragment.
- IgE immunoglobulin E
- IgE immunoglobulin E
- IgE is an antibody that is normally present in very low concentrations in serum. IgE is also normally produced by harmless antigens, and there are cases where IgE is increased without special stimulation, and in this case, allergic disease can be caused.
- Abnormally increased IgE can bind to the high affinity IgE Fc receptor (Fc ⁇ RI) expressed on the surface of mast cells and basophils and the like.
- Fc ⁇ RI IgE Fc receptor
- mast cells or basophilic granulocytes release chemical mediators such as histamine, leukotriene, prostaglandin, bradykinin and platelet-activating factor. Allergic symptoms are caused by the release of these chemical mediators.
- the antibody fragment according to the present invention can be used as a blocking agent of Fc epsilon receptor (Fc ⁇ RI) for suppressing allergic reactions.
- the present invention relates to a composition for inhibiting an autoimmune reaction comprising an antibody fragment.
- autoimmune diseases such as systemic lupus erythematosus (SLE) is a large amount of inflammatory cytokines (IFN- ⁇ , TNF, IL-6) caused by plasmacytoid dendritic cells (pDC). ) is secreted.
- pDC cells Like mast cells, pDC cells express Fc ⁇ RI on their surface, and upon activation, they can secrete 1,000 times more IFN- ⁇ than in other cell types.
- the complex (immune complex) of the IgE isotype autoantibody and DNA antigen binds to Fc ⁇ RI on the pDC surface, the immune complex enters the cell through Fc ⁇ RI and enters the cell.
- the immune complex that enters the cell stimulates intracellular receptors such as Toll-like receptor (TLR)-7 and -9 to activate pDC cells.
- TLR Toll-like receptor
- the antibody fragment according to the present invention may be used as a blocking agent of Fc epsilon receptor (Fc ⁇ RI) for suppressing autoimmune responses mediated by IgE autoantibodies.
- Fc ⁇ RI Fc epsilon receptor
- KV10-IgCw- ⁇ vector that simultaneously expresses human C ⁇ 1/ ⁇ 2-4 and human C ⁇ having a leader sequence by controlling two CMV promoters
- NcoI and NcoI of KV10-IgCW ⁇ vector A DNA fragment encoded by the hybridization of human heavy chain constant regions C ⁇ 1 and ⁇ 2-4 between the BamHI restriction sites was cloned.
- V H and V K domains were encoded. The fragment was cloned.
- a DNA fragment encoding human Fc ⁇ RI ⁇ was cloned between EcoI and BamHI restriction sites in pCDH-CMV-MCS-EF1-Puro vector.
- Example 1-2 Preparation of immunoglobulin protein using HEK293F cells
- a FreeStyleTM 293-F cell line (Thermo Fisher Scientific) adapted to grow in suspension culture in serum-free conditions was used for antibody production.
- FreeStyle HEK293F cells were placed in a 500ml flask (Corning Cat# 431145) and cultured at 1 ⁇ 10 6 cells/ml .
- FreeStyle 293-F cells were cultured by shaking at 130 rpm in a serum-free FreeStyle 293 medium (Invitrogen Cat# 12338) at 8% CO 2 , 37° C. in an incubator.
- IgCw- ⁇ , IgCw- ⁇ proteins 200 ⁇ g of KV plasmid encoding each gene and 400 ⁇ g of polyethyleneimine (PEI) reagent (Polyscience Cat# 23966-2) were placed in 5 ml of FreeStyle 293 medium, respectively, and placed at room temperature. was held for 10 min. Then, 5 ml of the medium containing DNA was filtered through a 0.22 ⁇ m syringe filter (Syringe filter, Millipore Cat# SLGV033RB), mixed with 5 ml of the medium containing polyethyleneimine, and placed at room temperature for 10 minutes.
- PEI polyethyleneimine
- transient transfection was performed on 100 ml of Freestyle 293-F cells so that the concentration of polyethyleneimine could be 4 ⁇ g/ml.
- the culture medium was centrifuged at 400g at 4°C for 20 minutes to obtain a supernatant, filtered through a 0.45 ⁇ m cellulose acetate filter (Sartorius Cat# 11106-47-N), and then CaptureSelectTM KappaXP (Thermo Fisher Scientific; Cat). # 2943212005) column or CaptureSelectTM IgG-CH1 (Thermo Fisher Scientific; Cat# 194320005) column.
- the protein was eluted with 0.1M glycine solution (glycine-HCl, pH 3.0).
- the eluted protein was concentrated using Vivaspin 20 (molecular cut-off 50,000, Sartorius Cat# VS2032) (4° C., 1500 g).
- the concentration of the purified protein was determined using absorbance at 280 nm and extinction coefficient. At 280 nm, the molar extinction coefficients were 1.49 for 6C407 IgE, 1.34 for IgCw- ⁇ , and 1.17 for IgCw- ⁇ , respectively, and were calculated from each amino acid sequence through http://web.expasy.org/protparam/ webpage.
- the RBL-2H3 (ATCC® number: CRL-2256TM) cell line derived from rat basophilic leukemia cells and the human embryonic kidney 293 cell line HEK293T (ATCC® number: CRL-3216TM) were obtained from Dulbecco's Modified Eagle's (DMEM). Medium, Welgene Inc.) cultured in medium. 10% fetal bovine serum (Sigma Inc.), 100 U/ml penicillin (penicillin, Welgene Inc.), and 100 ⁇ g/ml streptomycin (streptomycin, Welgene Inc.) were added to DMEM medium and used. All cells were cultured in 5% CO 2 , 37° C. incubator.
- DMEM Dulbecco's Modified Eagle's
- the human embryonic kidney 293 cell line HEK293T was used for the production of supernatant containing a lentivirus expressing Fc ⁇ RI ⁇ .
- HEK293T cells In order to have a cell number of 3 ⁇ 10 6 cells at the time of transfection, 24 hours before transfection, incubate HEK293T cells in a 60 mm 2 culture dish (SPL; Cat# 11060) at 1.5 ⁇ 10 6 cells/well in DMEM medium. 4 ml was added and cultured.
- a lentivirus-containing supernatant was prepared for expression of a receptor that recognizes human IgE in RBL-2H3 cells.
- RBL-2H3 cells were cultured in a 60 mm 2 culture dish with 4 ml of DMEM medium at 1 ⁇ 10 6 cells/well. After 24 hours, the medium was removed and the cells were washed once with PBS (phosphate-buffered saline, pH 7.4), mixed with 3 ml of DMEM and 1 ml of the lentivirus-containing supernatant, and then Polybrene (Sigma-Aldrich; Cat# H9268) concentration was added to be 10 ⁇ g/ml.
- PBS phosphate-buffered saline, pH 7.4
- the cells (1 ⁇ 10 6 cells) were washed with cold PBS and then diluted with 4% paraformaldehyde in PBS. was treated and fixed in the cells at room temperature for 20 minutes.
- the detection antibody APC-conjugated mouse anti-human Fc epsilon RI Ab (Abcam; Cat# 155369) was diluted in buffer S (0.5% BSA diluted in PBS, 2 mM EDTA, pH 8.5) and used. After standing at 4°C for 1 hour, it was washed three times with cold PBS. Analysis was performed via a FACS CantoII analyzer (BD Biosciences).
- the immunoglobulin protein was added to Fc ⁇ R-RBL-2H3, Fc ⁇ R+ RBL-2H3-hFc ⁇ RI ⁇ cells (1 ⁇ 10 6 cells) at a final concentration of 1 ⁇ M at 37°C. was treated for 3 hours. After washing the cells with cold PBS, the cells were treated with 4% paraformaldehyde diluted in PBS for 20 minutes at room temperature and fixed.
- RBL-2H3 and RBL-2H3-hFc ⁇ RI ⁇ cells were used as primary antibodies with goat anti-Human IgE ( ⁇ -chain specific) antibody (Sigma-Aldrich; Cat# I6284) and PE-conjugated donkey anti-goat IgG antibody (Abcam) as secondary antibodies. ; Cat# Ab7004) was diluted in buffer S and used. And it was washed three times with cold PBS for each fermentation step (4 °C, 1 hour). Each sample was analyzed through a FACS CantoII analyzer (BD Biosciences).
- Example 2-2 Enzyme-linked immunosorbent assay (ELISA) for measuring IgE concentration
- the wells of a 96-well polystyrene plate were treated with a coating antibody and coated at 4° C. for 16 hours. After that, each fermentation step (room temperature) was washed four times using TBS (TRIS-buffered saline; 50 mM TRIS-Cl, 50 mM NaCl, pH 7.4) containing 0.05% Tween-20. In order to block the binding of non-specific antibodies, 3% BSA (bovine serum albumin) was treated at room temperature for 2 hours.
- TBS TriS-buffered saline; 50 mM TRIS-Cl, 50 mM NaCl, pH 7.4
- BSA bovine serum albumin
- Human polyclonal IgE and IgCw- ⁇ were serially diluted two-fold at a starting concentration of 250 ng/ml, respectively, and the wells were treated at room temperature for 2 hours, and the detection antibody was treated at room temperature for 1 hour. Finally, the reaction substrate solution was added to each well, and absorbance was measured at 450 nm using a microplate reader (Molecular Devices Inc.).
- the coated antibody was coated on the wells of a 96-well polystyrene plate at 4°C for 16 hours. After treatment with monoclonal 6C407 IgE or 3D8 IgE, the detection antibody was treated (both treated at room temperature for 1 hour). The concentration of the IgE sample was determined by interpolation of Y-axis values from two different standard curves made using human IgE and IgCw- ⁇ , respectively, of known concentrations.
- Example 2-3 beta-hexosaminidase secretion measurement (Degranulation assay: beta hexosaminidase release assay)
- Beta-hexosaminidase secretion was measured to confirm whether the complex to which IgE and Fc ⁇ receptors are bound exhibits degranulation.
- RBL-2H3-hFc ⁇ RI ⁇ cells 5 ⁇ 10 5 cells/well, 24 hours before, 2.5 ⁇ 10 5 cells/well were cultured in a 24-well plate (SPL; Cat# 30024) with 400 ⁇ l of DMEM medium.
- IgE was added to 400 ⁇ l of DMEM medium without fetal bovine serum, penicillin, and streptomycin at a concentration of 10 nM and cultured for 3 hours.
- Siraganian buffer 119 mM NaCl, 5 mM KCl, 5.6 mM glucose, 0.4 mM MgCl 2 , 25 mM PIPES, 40 mM NaOH, 1 mM CaCl 2 , 0.1% BSA, pH 7.2. washed. 160 ⁇ l of Siraganian buffer was placed in an incubator at 5% CO 2 , 37° C. for 10 minutes. Goat anti-Human Kappa Light chain antibody (Invitrogen; Cat# 31129) was mixed with Siraganian buffer to a final concentration of 10 ⁇ g/ml, then 20 ⁇ l of each was added to the well and allowed to stand for 20 minutes.
- Siraganian buffer 119 mM NaCl, 5 mM KCl, 5.6 mM glucose, 0.4 mM MgCl 2 , 25 mM PIPES, 40 mM NaOH, 1 mM CaCl 2 , 0.1% BSA, pH 7.2.
- Triton X-100 used as a control was placed in an incubator at 5% CO 2 , 37° C. for 1 hour. After incubation for 20 minutes in 5% CO 2 , 37°C incubator, 50 ⁇ l of each was added to the wells of a 96-well polystyrene plate, and then 1 mM p-NAG (p-nitrophenyl N-acetyl-beta-D-glucosamine) was added. in 0.1 M citrate buffer, pH 4.5) was added 50 ⁇ l each. After treatment at 37° C.
- Example 2-4 beta-hexosaminidase secretion measurement to confirm the role of a blocker of the Fc ⁇ receptor
- Beta-hexosaminidase secretion was measured to determine whether the complex in which the IgE and Fc ⁇ receptors are combined acts as a blocker of the Fc ⁇ receptor, which serves to prevent degranulation by other IgE.
- 400 ⁇ l of DMEM medium was added to a 24-well plate at 2.5 ⁇ 10 5 cells/well 24 hours before incubation.
- IgCw- ⁇ consisting only of the constant regions of the epsilon heavy chain and the kappa light chain did not form a disulfide bond between the heavy and light chain constant regions, so only the kappa constant region could be purified ( FIG. 2 ).
- the antibody fragment IgCw- ⁇ which consists of the constant regions of the heavy and light chains fused with the gamma constant region (C ⁇ 1) and the epsilon constant region (C ⁇ 2-4), disulfide bonds between the constant regions are normally formed, and the expression level is also control 6C407 Similar to IgE (Fig.
- the average yield is ⁇ 17 mg/L, the same as 6C407 IgE, when purified with KappaXP-agarose, and ⁇ 27 mg/L when purified with IgG-CH1-agarose (Table 1) ).
- the anti-Fc ⁇ antibody did not bind to wild-type RBL-2H3 cells, but bound to RBL-2H3-hFc ⁇ RI ⁇ cells expressing Fc ⁇ receptors ( FIG. 3 ). This means that human Fc ⁇ receptor is not expressed in wild-type RBL-2H3 cells, but is present only in RBL-2H3-hFc ⁇ RI ⁇ cells expressing human Fc ⁇ receptor.
- IgCw- ⁇ binds to RBL-2H3-hFc ⁇ RI ⁇ cells made to express hFc ⁇ RI ⁇ , but not to RBL-2H3 cells lacking any hFc ⁇ RI ⁇ ( FIG. 3 ). This means that IgCw- ⁇ can recognize Fc ⁇ receptors like full-size IgE.
- Example 6 Use of IgCw- ⁇ as a reference for degranulation experiments using IgE
- IgCw- ⁇ could be used instead of full-size IgE in experiments in which IgE is used, such as degranulation assay experiments, was confirmed by beta-hexosaminidase secretion experiments.
- Example 7 Use of IgCw- ⁇ as a blocker of Fc ⁇ receptors
- IgCw- ⁇ could be used as a blocker of the Fc ⁇ receptor.
- IgCw- ⁇ does not have a variable region, it cannot bind to Protein L, so the activation signal of RBL-2H3-hFc ⁇ RI ⁇ cells can be observed only when full-size IgE binds to Fc ⁇ .
- FIG. 5B When 6C407 IgE and IgCw- ⁇ mixture was treated in RBL-2H3-hFc ⁇ RI ⁇ cells (FIG. 5B), as well as when 6C407 IgE was pretreated in RBL-2H3-hFc ⁇ RI ⁇ cells and then treated with IgCw- ⁇ (FIG. 5C)
- the concentration of IgCw- ⁇ increased, the signal for 6C407 IgE decreased ( FIG. 5 ). This indicates that IgCw- ⁇ could be used as a blocker of the Fc ⁇ receptor because it means that IgCw- ⁇ prevented the binding of full-size IgE to the Fc ⁇ receptor.
- Example 8 Use of IgCw- ⁇ as a reference for quantification of IgG concentration
- IgCw- ⁇ could be used as a substitute for full-size IgE, a reference used to determine the IgG concentration.
- Normalized concentrations of 6C407 IgE and 3D8 IgE were 75.366 ng/ml and 24.737 ng/ml, respectively, which were determined by a standard curve using human polyclonal antibodies (6C407 IgE: 70.42 ng/ml, 3D8 IgE: 25.01 ng/ml). ml) is very similar. This indicates that IgCw- ⁇ can be used as a reference molecule for determining human IgE concentrations.
- the antibody fragment according to the present invention can be widely used as a substitute for the IgE reference antibody used in various immunological studies. It can be used as a reference molecule for measuring the concentration of IgE antibody in a sample, and can be used as a blocking agent of Fc epsilon receptor (Fc ⁇ RI) for suppressing type 1 allergic reaction.
- Fc ⁇ RI Fc epsilon receptor
- the antibody fragment according to the present invention can be used as a blocking agent for suppressing autoimmune reactions related to autoantibodies of the IgE isotype.
- the antibody fragment according to the present invention does not include a variable region, the non-specific cross-reaction, which is a disadvantage of the full-length isotype control antibody used in the past, that is, the off-target effect caused by the reaction with other antigens is completely eliminated.
- the non-specific cross-reaction which is a disadvantage of the full-length isotype control antibody used in the past, that is, the off-target effect caused by the reaction with other antigens is completely eliminated.
- it can be used more suitably in quantitative and qualitative experiments of IgE, and can be used as an isotype control antibody in the evaluation of effectiveness for the activity of experimental/therapeutic antibodies.
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Abstract
Description
Claims (14)
- IgG 항체의 중쇄 불변부위(constant region) 단편 및 IgE 항체의 중쇄 불변부위 단편; 및 상기 중쇄 불변부위 단편과 연결된 경쇄 불변부위 단편을 포함하는 항체 단편.
- 제1항에 있어서, 항체의 가변부위(variable domains)를 포함하지 않는 것을 특징으로 하는 항체 단편.
- 제1항에 있어서, 상기 IgG 항체의 중쇄 불변부위 단편은 Cγ1을 포함하는 항체 단편.
- 제1항에 있어서, 상기 IgE 항체의 중쇄 불변부위 단편은 Cε2, Cε3 및 Cε4로 구성된 군에서 선택되는 하나 이상을 포함하는 항체 단편.
- 제1항에 있어서, 상기 IgG 항체의 중쇄 불변부위(constant region) 단편 및 IgE 항체의 중쇄 불변부위 단편은 힌지 (hinge)를 통해 연결되는 것을 특징으로 하는 항체 단편.
- 제1항에 있어서, 상기 IgG 항체의 중쇄 불변부위 단편 및 IgE 항체의 중쇄 불변부위 단편은 N 말단에서 C 말단 방향으로 Cγ1-Cε2-Cε3-Cε4로 연결되는 것을 특징으로 하는 항체 단편.
- 제1항에 있어서, 상기 경쇄 불변부위는 Cκ 또는 Cλ를 포함하는 것을 특징으로 하는 항체 단편.
- 제1항에 있어서, 상기 중쇄 불변부위 단편과 연결된 경쇄 불변부위 단편은 이황화결합(disulfide bond)에 의해 결합되거나, 또는 펩티드 링커(linker)로 결합된 것을 특징으로 하는 항체 단편.
- 제1항 내지 제8항 중 어느 한 항의 항체 단편을 코딩하는 핵산.
- 제1항 내지 제8항 중 어느 한 항의 항체 단편을 포함하는 키트.
- 제1항 내지 제8항 중 어느 한 항의 항체 단편을 포함하는 항체 효능 평가용 조성물.
- 제1항 내지 제8항 중 어느 한 항의 항체 단편을 포함하는 항체 농도 측정용 조성물.
- 제1항 내지 제8항 중 어느 한 항의 항체 단편을 포함하는 알러지 반응 억제용 조성물.
- 제1항 내지 제8항 중 어느 한 항의 항체 단편을 포함하는 자가면역 반응 억제용 조성물.
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AU2021329742A AU2021329742A1 (en) | 2020-08-21 | 2021-08-20 | Antibody fragment consisting of heavy chain and light chain constant regions in which gamma constant region (CΓ1) and epsilon constant region (CE2-4) are fused, and use thereof |
CN202180063851.9A CN116194487A (zh) | 2020-08-21 | 2021-08-20 | 由重链恒定区和轻链恒定区组成的γ恒定区(Cγ1)和ε恒定区(Cε2-4)融合的抗体片段及其用途 |
CA3189721A CA3189721A1 (en) | 2020-08-21 | 2021-08-20 | Antibody fragment consisting of heavy chain and light chain constant regions in which gamma constant region (c.gamma.1) and epsilon constant reggion (c.epsilon.2-4) are fused, and use thereof |
US18/022,394 US20230322860A1 (en) | 2020-08-21 | 2021-08-20 | ANTIBODY FRAGMENT CONSISTING OF HEAVY CHAIN AND LIGHT CHAIN CONSTANT REGIONS IN WHICH GAMMA CONSTANT REGION (Cgamma1) AND EPSILON CONSTANT REGION (CE2-4) ARE FUSED, AND USE THEREOF |
JP2023512658A JP2023538927A (ja) | 2020-08-21 | 2021-08-20 | ガンマ定常領域(Cγ1)とイプシロン定常領域(Cε2-4)とが融合された重鎖及び軽鎖の定常領域からなる抗体断片及びその用途 |
EP21858634.5A EP4201962A1 (en) | 2020-08-21 | 2021-08-20 | Antibody fragment consisting of heavy chain and light chain constant regions in which gamma constant region (c?1) and epsilon constant region (c?2-4) are fused, and use thereof |
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2021
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- 2021-08-20 EP EP21858634.5A patent/EP4201962A1/en active Pending
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