JP7210818B2 - T細胞免疫療法のための組合せ及びその使用 - Google Patents
T細胞免疫療法のための組合せ及びその使用 Download PDFInfo
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Description
[6]本発明は、驚くべきことに、2重特異性T細胞活性化抗原結合分子はエフェクター記憶γ9δ2T細胞と一緒に患者に投与することができ、このような投与によって免疫療法の治療効果を相乗的に高めることができることを発見した。
[25]本明細書で使用する場合、用語「抗原結合分子」は、最も広い意味で、抗原決定基に特異的に結合する分子を意味する。抗原結合分子の例は、完全長又は完全な構造のイムノグロブリンの分子及び/又はその機能的断片及び/又は抗体から得られた可変重鎖(VH)及び/又は可変軽鎖(VL)ドメインなどの、イムノグロブリン及びそれらの誘導体である。したがって、抗原結合分子は特異的標的又は抗原に結合することができる。抗原結合分子は、少なくとも3つの軽鎖CDR(すなわち、VL領域のCDR1、CDR2及びCDR3)、及び/又は3つの重鎖CDR(すなわち、VH領域のCDR1、CDR2及びCDR3)を有し、並びに好ましくは6つのCDR全てを有している。抗原結合分子に基づいた抗体には、例えば、モノクローナル、組換え、キメラ、ヒト化及びヒト抗体が含まれる。
[51]本発明は、驚くべきことに、エフェクター記憶γ9δ2T細胞及び2重特異性T細胞活性化抗原結合分子を組み合わせて患者に投与したとき、2重特異性T細胞活性化抗原結合分子が媒介するT細胞免疫療法の治療効果を相乗的に増強することができることを見出した。したがって、本発明の実施形態の1つは、治療有効量の2重特異性T細胞活性化抗原結合分子及び治療有効量のエフェクター記憶γ9δ2T細胞を、それらを必要とする対象に投与し、それらを必要とする対象のがん、感染性疾患、及び/又は免疫障害などの疾患を治療するために使用することができる併用療法である。別の実施形態では、本発明は、疾患を治療するための医薬品の製造における、2重特異性T細胞活性化抗原結合分子と組み合わせたエフェクター記憶γ9δ2T細胞の使用を提供する。
(a)第1の抗原に特異的に結合する第1の抗原結合部分であって、第1の抗原がT細胞を活性化するCD3である、第1の抗原結合部分、並びに
(b)第2の抗原に特異的に結合する第2の抗原結合部分であって、第2の抗原が腫瘍細胞ネオ抗原、腫瘍ネオエピトープ、腫瘍特異的抗原、腫瘍関連抗原、組織特異的抗原、細菌抗原、ウイルス抗原、酵母抗原、真菌抗原、原生動物抗原及び寄生生物抗原からなる群から選択される、第2の抗原結合部分を含む。
[59]本発明は、治療有効量の2重特異性T細胞活性化抗原結合分子及び治療有効量のエフェクター記憶γ9δ2T細胞を含む組合せであって、2重特異性T細胞活性化抗原結合分子を対象にエフェクター記憶γ9δ2T細胞の投与と同時、前又は後に投与することができる組合せをさらに提供する。
[63]別の実施形態では、本発明は、前述のような疾患の治療のために適切な物質を含むキットを提供する。キットには、容器及び容器に入れた、又は付随した指示物又は添付文書が含まれる。適切な容器には、例えば、瓶、バイアル、シリンジ、IV溶液バッグなどが含まれる。容器は、ガラス又はプラスティックなどの種々の材料から形成することができる。容器は、組成物を単独又は疾患を治療するために有効な別の組成物と組み合わせて保持し、滅菌した接続口を有していてもよい(例えば、容器は皮下注射針によって貫通することができる栓を備えた静脈注射用溶液バッグ又はバイアルであってもよい)。組成物中の少なくとも1つの活性剤は、本発明の2重特異性T細胞活性化抗原結合分子又はエフェクター記憶γ9δ2T細胞である。指示物又は添付文書は、選択した症状を治療するために組成物を使用することを指示している。さらに、キットは、(a)キットに含有される第1の組成物を含む第1の容器であって、第1の組成物が本発明の2重特異性T細胞活性化抗原結合分子を含む容器、及び(b)キットに含有される第2の組成物を含む第2の容器であって、第2の組成物がエフェクター記憶γ9δ2T細胞を含む容器を含んでいてもよい。本発明のこの実施形態におけるキットは、組成物が特定の症状を治療するために使用することができることを指示している添付文書をさらに含んでいてもよい。或いは、又は追加的に、キットは免疫抑制剤を含む第3の容器をさらに含んでいてもよい。容器は、商用及び使用者の観点から所望される、その他の緩衝剤、希釈剤、充填剤、針及びシリンジを含むその他の材料をさらに含んでいてもよい。
γ9δ2T細胞の単離及び同定
[65]本発明のために、血液がん細胞を殺滅する能力を有するエフェクター記憶γ9δ2T細胞を増殖させることが最初に必要である。γ9δ2T細胞は、抗CD3抗体、抗γ9抗体及び抗δ2抗体を使用したフローサイトメトリーによって同定することができる。エフェクター記憶γ9δ2T細胞の特徴の1つは、細胞表面にCD27及びCD45RA分子がないことである。
血液がん細胞の殺滅に対するγ9δ2T細胞及びBLINCYTO(登録商標)(BiTE)の活性のインビトロアッセイ
[68]実験は、Sheehyら(J Immunol Methods、249、99~110(2001))で開示された方法に従って実施した。
[72]実験は、Sheehyら(J Immunol Methods、249、99~110(2001))で開示された方法に従って実施した。BCMA-BiTEは、国際公開第2013/072415号に従って調製した。
免疫不全NOGマウスモデルにおける血液がん細胞の殺滅に対するγ9δ2T細胞及びBLINCYTO(登録商標)の活性のインビボアッセイ
[76]この実験は、T細胞が欠如している免疫不全NOGマウス(Hippら、Leukemia、31、1~9(2017)及びMonjeziら、Leukemia、30、1~9(2016)を参照のこと)において実施した。
γ9δ2T細胞及びBLINCYTO(登録商標)で治療した免疫不全NOGマウスの生存についての研究
[79]この実験では、T細胞が欠如している免疫不全NOGマウスを、骨髄移植を受けた後に早期再発している(T細胞の数が非常に少ないか、又は機能性T細胞(例えば、記憶T細胞)が欠如している)患者をシミュレートするために使用した。
免疫不全NOGマウスにおける骨髄外疾患のためのγ9δ2T細胞及びBLINCYTO(登録商標)の併用療法についての研究
[84]BLINCYTO(登録商標)は、合衆国において2年超に亘って販売されている。臨床適用におけるBLINCYTO(登録商標)の効果を分析したとき、Aldossら(AM J Hematol.、92、858~865(2017))は、もし患者がBLINCYTO(登録商標)による治療の前に骨髄外疾患を有していたならば、BLINCYTO(登録商標)の臨床治療効果は不十分であることを発見した。さらに、BLINCYTO(登録商標)による治療を受けた後再発した患者の最高40%が骨髄外疾患を有していた。
Claims (10)
- 治療を必要とする対象の血液がんの治療において使用するための医薬組成物であって、
治療有効量のブリナツモマブを含み、
治療有効量のCD27(-)及びCD45RA(-)エフェクター記憶γ9δ2T細胞と組み合わせて使用することを特徴とし、
前記エフェクター記憶γ9δ2T細胞がプログラム死-1(PD-1)を発現しておらず、前記エフェクター記憶γ9δ2T細胞がエキソビボにおいて増殖するものである、医薬組成物。 - 前記エフェクター記憶γ9δ2T細胞がそれらを必要とする前記対象に対して自己由来又は同種である、請求項1に記載の医薬組成物。
- ブリナツモマブが医薬組成物に製剤化されている、請求項1又は2に記載の医薬組成物。
- 前記エフェクター記憶γ9δ2T細胞が医薬組成物に製剤化されている、請求項1~3のいずれか一項に記載の医薬組成物。
- 前記血液がんが、非ホジキンリンパ腫又は急性リンパ芽球性白血病又は慢性リンパ性白血病である、請求項1~4のいずれか一項に記載の医薬組成物。
- 前記急性リンパ芽球性白血病が再燃性又は治療抵抗性急性リンパ芽球性白血病である、請求項5に記載の医薬組成物。
- 治療を必要とする対象の血液がんの治療において使用するためのキットであって、
ブリナツモマブ、CD27(-)及びCD45RA(-)エフェクター記憶γ9δ2T細胞及びそれらを必要とする対象の治療するべき血液がんを指示している添付文書を含み、
前記エフェクター記憶γ9δ2T細胞がプログラム死-1(PD-1)を発現しておらず、前記エフェクター記憶γ9δ2T細胞がエキソビボにおいて増殖するものである、キット。 - 前記エフェクター記憶γ9δ2T細胞がそれらを必要とする前記対象に対して自己由来又は同種である、請求項7に記載のキット。
- ブリナツモマブが医薬組成物に製剤化されている、請求項7又は8に記載のキット。
- 前記エフェクター記憶γ9δ2T細胞が医薬組成物に製剤化されている、請求項7又は8に記載のキット。
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