JP2017500889A - Pd−1抗体、その抗原結合性断片及びそれらの医学的使用 - Google Patents
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Abstract
Description
配列番号6、配列番号7または配列番号8に示される配列から選択される少なくとも1つのLCDRを含む軽鎖可変領域;及び
配列番号3、配列番号4または配列番号5に示される配列から選択される少なくとも1つのHCDRを含む重鎖可変領域。
本発明をより容易に理解するために、ある種の技術用語及び科学用語を具体的に以下で定義する。本明細書の他の個所で特に定義されない限り、本明細書で使用されるすべての他の技術用語及び科学用語は、本発明が属する分野の当業者によって一般に理解される意味を有する。
以下に、実施例を参照して本発明をさらに説明するが、本発明の範囲はそれらに限定されない。本発明の実施例では、特定の条件が説明されない場合、実験は、Antibody Tcchnology Laboratory Manual and Mecular Cloning Manual of Cold Spring Harborに記載されているような従来の条件下で、または材料もしくは製品の製造者が提案する条件下で、通常行われる。試薬の供給源が特に示されない場合は、その試薬は市販の従来の試薬である。
ヒトPD−1に対するマウスモノクローナル抗体を生成した。精製した組み換えPD−1細胞外ドメインFc融合タンパク質(PD−1 Fc)(配列番号1);またはPD−1をトランスフェクトしたCHO細胞(配列番号2)を抗原として使用して、Balb/Cマウス及びSJLマウスを免疫化した。ヒトPD−1抗原は、ORIGENE(カタログ番号SC117011、NCBI参照配列:NM_005018.1)から購入した。
インビトロでのPD−1抗体のELISA結合アッセイ:
PD−1抗体は、PD−1細胞外ドメインに結合することによって、PD−1及びそのリガンドのシグナル伝達経路をブロックする。インビトロでのELISAアッセイを使用して、PD−1抗体の結合特性を検出する。ビオチン標識したPD−1細胞外ドメインFC融合タンパク質(PD−1 FC)を、中和アビジンに結合させることによって96ウェルプレートにコーティングする。抗体添加後のシグナル強度を使用して、抗体及びPD−1の結合特性を決定する。
腫瘍細胞の表面のPD−L1は、T細胞の表面のPD−1に結合することによって、T細胞の増殖に対して抑制作用を示す。PD−1抗体は、T細胞増殖を刺激するために、PD−1に結合することによって、PD−L1/PD−1シグナル伝達経路をブロックする。PD−1/PD−L1結合ブロッキングアッセイを使用して、このシグナル伝達経路に対するPD−1抗体のブロッキング活性を検出する。
PD−1ファミリーの他のタンパク質へのPD−1抗体の特異的結合活性を検出するために、ヒトCTLA4及びヒトCD28を結合アッセイに使用した。その一方で、ヒト/サル以外の異なる種に対するPD−1抗体の多様性を確認するために、マウスのPD−1も結合アッセイに使用した。
FACS(蛍光活性化セルソーター)は、タンパク質と細胞の相互作用を検出する試験方法である。この試験を使用して、細胞表面で発現している天然のPD−1に対するPD−1抗体の結合活性を検出する。この試験で使用する細胞は、PD−1を高発現するCHO細胞である(実施例1、PD−1をトランスフェクトしたCHO細胞(配列番号2)を参照されたい)。
Biacore法は、タンパク質の相互作用的親和性及び動態を客観的に検出する、認められているアッセイである。本発明者らは、Biacore(GE)によって、本発明の試験PD−1抗体の特徴付けられた親和性及び結合動態を解析した。
抗体の影響を受ける、新鮮なヒト末梢血単核球(PBMC)の増殖アッセイを使用して、抗体mAb005の細胞活性を検出する。
mAb005抗体の軽鎖可変領域の配列(mAb005 LCVR、配列番号10)及び重鎖可変領域の配列(mAb005 HCVR、配列番号9)に関して、生殖細胞系データベースにおいてその非CDRと最もよく一致するヒト化鋳型を選択した。抗体重鎖の鋳型はIgHV3−7/JH6であり、ヒト生殖細胞系軽鎖IGKV1−39のFR1、FR2、FR3及びJK4のFR4について選択し、配列番号13の配列を有し;軽鎖の鋳型はIGKV1−39/JK4であり、ヒト生殖細胞系軽鎖IGKV1−39のFR1、FR2、FR3及びJK4のFR4について選択し、配列番号14の配列を有する。
ヒト生殖細胞系重鎖の鋳型(配列番号13):
ヒト生殖細胞系軽鎖の鋳型(配列番号14):
抗体の表示
ヒト化抗体を、インビトロで、ELISA結合アッセイ(方法は実施例2のものと同じである)、リガンド結合ブロッキングアッセイ(方法は実施例2のものと同じである)及び親和性動態実験(方法は実施例5のものと同じである)にかけた。結果を以下の表に示す:
1.実験材料:
U87MG 細胞(神経膠腫細胞):Chinese Academy of Sciences Cell Bankから購入した(カタログ番号TCHu138);
Shanghai Blood Centerから購入したPBMC(末梢血単核球);
CD3:Miltenyi Biotecから購入した(カタログ番号130−093−387);
CD28:Miltenyi Biotecから購入した(カタログ番号130−093−375);
細胞計数キット−8:DOJINDO LABORATORIESから入手可能(カタログ番号CK04);
mIgG(陰性対照):SANTA CRUZから購入した(カタログ番号sc−2025);1660ng/mlの用量を使用。
1)10%FBS及び1%P/Sを含むEMEM培地中でU87MG細胞を培養し、96ウェルプレート(ウェルあたり1×104細胞)でインキュベートした。
2)H005−1抗体をPBSで異なる濃度勾配(図3の横軸に示す)に希釈し、10ul/ウェルで96ウェルプレートに加え、37℃、5%CO2のインキュベーター中で4時間インキュベートした。
3)細胞が接着した後、2×104細胞/ウェルの細胞密度で80ulのPBMC細胞懸濁液を各ウェルに加え、10ulのCD3抗体及びCD28抗体を各ウェルに加え、CD3及びCD28抗体の終濃度は両方とも500ng/mlであった。
4)37℃、5%CO2のインキュベーター中で72時間インキュベートした後、10ulのCCK8を各ウェルに加えて顕色させ、2時間後、OD450を測定した。
結果を図3に示した。mIgG(陰性対照)と比較した場合、異なる濃度のPD−1抗体(H005−1)がU87MG細胞の成長に対して有意な阻害作用を有しており、最高濃度の阻害率は約30%であった。
インビトロでのツベルクリン刺激性のPBMC増殖に対するヒト化抗体H005−1の活性を検出した。
ツベルクリン刺激性のPBMC増殖及びIFN−γ分泌に対する試験試料の活性化作用
100ulのU87細胞(5×106細胞)をSCID−Beigeマウスの右肋骨部に皮下接種した。7〜10日後に腫瘍が80〜100mm3に成長した時に、大きすぎるまたは小さすぎる体重または腫瘍を有するものを除いて、腫瘍体積に従って、SCID−BeigeマウスをH005−1の10mg/kg群とヒトIgGの10mg/kg群にランダムに分け、各群は7匹のマウスとした(D0)。3日間CD3抗体で刺激した2種類のPBMCを1:1の比で混合し、5×105細胞/60ulで腫瘍組織に注射し、その間に、試験抗体を、全部で3回の投与にわたって7日に1回皮下に注射した。週2回、マウスを腫瘍体積について測定し、計量した。データを記録した。腫瘍体積(V)を、V=1/2×a×b2(式中、a及びbはそれぞれ長さ及び幅を表す)として計算した。
Claims (27)
- 以下を含む、PD−1抗体またはその抗原結合性断片:
配列番号6、配列番号7または配列番号8に示される配列から選択される少なくとも1つのLCDRを含む軽鎖可変領域;及び
配列番号3、配列番号4または配列番号5に示される配列から選択される少なくとも1つのHCDR領域を含む重鎖可変領域。 - 前記軽鎖可変領域が配列番号6に示されるLCDR1を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記軽鎖可変領域が配列番号7に示されるLCDR2を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記軽鎖可変領域が配列番号8に示されるLCDR3を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記重鎖可変領域が配列番号3に示されるHCDR1を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記重鎖可変領域が配列番号4に示されるHCDR2を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記重鎖可変領域が配列番号5に示されるHCDR3を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記軽鎖可変領域が、それぞれ配列番号6、配列番号7及び配列番号8に示されるLCDR1、LCDR2及びLCDR3を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記重鎖可変領域が、それぞれ配列番号3、配列番号4及び配列番号5に示されるHCDR1、HCDR2及びHCDR3を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記軽鎖可変領域が、それぞれ配列番号6、配列番号7及び配列番号8に示されるLCDR1、LCDR2及びLCDR3を含み;前記重鎖可変領域が、それぞれ配列番号3、配列番号4及び配列番号5に示されるHCDR1、HCDR2及びHCDR3を含む、請求項1に記載のPD−1抗体またはその抗原結合性断片。
- 前記抗体または前記その抗原結合性断片がマウス抗体またはその断片である、請求項1〜10のいずれか1項に記載のPD−1抗体またはその抗原結合性断片。
- 前記抗体または前記その抗原結合性断片がキメラ抗体またはその断片である、請求項1〜10のいずれか1項に記載のPD−1抗体またはその抗原結合性断片。
- 前記キメラ抗体の前記軽鎖可変領域配列が配列番号10である、請求項12に記載のPD−1抗体またはその抗原結合性断片。
- 前記キメラ抗体の前記重鎖可変領域配列が配列番号9である、請求項12に記載のPD−1抗体またはその抗原結合性断片。
- 前記抗体または前記抗原結合性断片がヒト化抗体またはその断片である、請求項1〜10のいずれか1項に記載のPD−1抗体またはその抗原結合性断片。
- 前記ヒト化抗体の前記軽鎖可変領域の前記軽鎖FR配列が、IGKV1−39のFR1、FR2及びFR3並びにJK4のFR4を含む、配列番号14に示される、ヒト生殖細胞系軽鎖IGKV1−39とJK4の組み合わせ配列に由来する、請求項15に記載のPD−1抗体またはその抗原結合性断片。
- 前記ヒト化抗体の軽鎖の前記配列が、配列番号12に示される配列またはその変異体であり;ここでは、前記変異体が、好ましくは、前記軽鎖可変領域中に0〜10個のアミノ酸変異、より好ましくはA43Sを含む、請求項15に記載のPD−1抗体またはその抗原結合性断片。
- 前記ヒト化抗体の前記重鎖可変領域が、ヒトのIgG1、IgG2、IgG3もしくはIgG4またはそれらの変異体の重鎖FR、好ましくはヒトのIgG2またはIgG4の重鎖FRをさらに含む、請求項15に記載のPD−1抗体またはその抗原結合性断片。
- 前記ヒト化抗体の前記重鎖可変領域の前記重鎖FR配列が、IgHV3−7のFR1、FR2及びFR3並びにJH6のFR4を含む、配列番号13で示される、ヒト生殖細胞系重鎖IgHV3−7とJH6の組み合わせ配列に由来する、請求項15に記載のPD−1抗体またはその抗原結合性断片。
- 前記ヒト化抗体重鎖の前記配列が、配列番号11に示される配列またはその変異体であり;ここでは、前記変異体が、好ましくは前記重鎖可変領域中に0〜10個のアミノ酸変異、より好ましくはG44Rを含む、請求項15に記載のPD−1抗体またはその抗原結合性断片。
- 請求項1〜20のいずれか1項に記載の抗体をコードするDNA分子。
- 請求項21に記載のDNA分子を含む発現ベクター。
- 請求項22に記載の発現ベクターで形質転換された宿主細胞。
- 前記宿主細胞が細菌、好ましくは大腸菌(E.coli)である、請求項23に記載の宿主細胞。
- 前記宿主細胞が酵母、好ましくはピキア・パストリス(Pichia pastoris)である、請求項23に記載の宿主細胞。
- 請求項1〜20のいずれか1項に記載のPD−1抗体または抗原結合性断片及び医薬的に許容可能な賦形剤、希釈剤または担体を含む、医薬組成物。
- PD−1媒介性の疾患または障害を処置するための医薬の調製における、請求項1〜20のいずれか1項に記載のPD−1抗体または抗原結合性断片及び請求項26に記載の医薬組成物の使用であって、前記疾患または障害が、好ましくは癌、より好ましくはPD−L1を発現している癌、最も好ましくは乳癌、肺癌、胃癌、腸癌、腎臓癌、黒色腫及び非小細胞肺癌、最も好ましくは非小細胞肺癌、黒色腫及び腎臓癌である、使用。
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JP2020505386A (ja) * | 2017-01-20 | 2020-02-20 | タユー ファシャ バイオテック メディカル グループ カンパニー, リミテッド | 抗pd−1抗体およびその使用 |
JP7275030B2 (ja) | 2017-01-20 | 2023-05-17 | タユー ファシャ バイオテック メディカル グループ カンパニー, リミテッド | 抗pd-1抗体およびその使用 |
JP2021508699A (ja) * | 2017-12-29 | 2021-03-11 | 江蘇恒瑞医薬股▲ふん▼有限公司 | トリプルネガティブ乳がんを処置するためのpd−1抗体及びアパチニブの併用処置の使用 |
JP2022514962A (ja) * | 2018-12-21 | 2022-02-16 | 神州細胞工程有限公司 | ヒト化抗pd-1抗体及びこの使用 |
JP7358478B2 (ja) | 2018-12-21 | 2023-10-10 | 神州細胞工程有限公司 | ヒト化抗pd-1抗体及びこの使用 |
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