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重组抗 EGFR×抗 CD3 双特异性抗体武装的激活 T 细胞对实体瘤的广泛反应性和增强效力。

Broad reactivity and enhanced potency of recombinant anti-EGFR × anti-CD3 bispecific antibody-armed activated T cells against solid tumours.

机构信息

Department of Medicine, Division of Hematology and Oncology, University of Virginia Cancer Center, Charlottesville, VA, USA.

TransTarget, Inc., Sunnyvale, CA, USA.

出版信息

Ann Med. 2022 Dec;54(1):1047-1057. doi: 10.1080/07853890.2022.2059101.

Abstract

Bispecific antibody (BiAb)-armed activated T cells (BATs) comprise an adoptive T cell therapy platform for treating cancer. Arming activated T cells (ATC) with anti-CD3 x anti-tumour associated antigen (TAA) BiAbs converts ATC into non-major histocompatibility complex (MHC)-restricted anti-tumour cytotoxic T lymphocytes (CTLs). Binding of target antigens via the BiAb bridge enables specific anti-tumour cytotoxicity, Th1 cytokines release, and T cell proliferation. Clinical trials in breast, prostate, and pancreatic cancer using BATs armed with chemically heteroconjugated BiAbs demonstrated safety, feasibility, induction of anti-tumour immune responses and potential increases in overall survival (OS). The primary objective of this study was to develop a recombinant BiAb that confers enhanced anti-tumour activity of BATs against a broad range of solid tumours. A recombinant anti-epidermal growth factor receptor (EGFR) x anti-CD3 (OKT3) BiAb (rEGFRBi) was designed and expressed in CHO cells, used to arm ATC (rEGFR-BATs), and tested for specific cytotoxicity against breast, pancreatic and prostate cancers and glioblastoma. rEGFR-BATs exhibit remarkably enhanced specific cytotoxicity and T1 cytokine secretion against a wide range of solid tumour cell lines vs. their respective chemically-heteroconjugated BATs. rEGFR-BATs may provide a "universal" T cell therapy for treating a wide range of solid tumours. KEY MESSAGEA (Gly4Ser)6 linker between the variable light and heavy chains of an scFv fused to the N-terminus of a heavy chain antibody confers unexpected stability to the heavy chain fusion protein and supports the efficient expression of the bispecific antibody.Arming of activated T cells with the rEGFRBi greatly enhances the relative cytotoxicity and Th1 cytokine secretion of theT cells relative to a chemically heteroconjugated BiAbs.rEGFR-BATs are promising candidates for the treatment of a broad range of solid tumours.

摘要

双特异性抗体 (BiAb)-武装的激活 T 细胞 (BATs) 构成了一种过继性 T 细胞治疗平台,用于治疗癌症。用抗-CD3 x 抗肿瘤相关抗原 (TAA) BiAb 武装激活 T 细胞 (ATC) 将 ATC 转化为非主要组织相容性复合体 (MHC) 限制的抗肿瘤细胞毒性 T 淋巴细胞 (CTL)。通过 BiAb 桥结合靶抗原可实现特异性抗肿瘤细胞毒性、Th1 细胞因子释放和 T 细胞增殖。在乳腺癌、前列腺癌和胰腺癌中使用化学异质共轭 BiAb 武装的 BATs 的临床试验证明了其安全性、可行性、诱导抗肿瘤免疫反应和潜在的总生存期 (OS) 增加。本研究的主要目的是开发一种重组 BiAb,赋予 BATs 针对广泛的实体瘤的增强抗肿瘤活性。设计并在 CHO 细胞中表达了一种抗表皮生长因子受体 (EGFR) x 抗-CD3 (OKT3) BiAb (rEGFRBi),用于武装 ATC (rEGFR-BATs),并测试其针对乳腺癌、胰腺癌和前列腺癌和胶质母细胞瘤的特异性细胞毒性。rEGFR-BATs 对广泛的实体瘤细胞系表现出显著增强的特异性细胞毒性和 T1 细胞因子分泌,与各自的化学异质共轭 BATs 相比。rEGFR-BATs 可为治疗广泛的实体瘤提供一种“通用”T 细胞疗法。关键信息 scFv 的可变轻链和重链之间的 (Gly4Ser)6 接头融合到重链抗体的 N 端赋予重链融合蛋白意想不到的稳定性,并支持双特异性抗体的有效表达。用 rEGFRBi 武装激活的 T 细胞可大大增强 T 细胞的相对细胞毒性和 Th1 细胞因子分泌,与化学异质共轭 BiAb 相比。rEGFR-BATs 是治疗广泛的实体瘤的有前途的候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed34/9045764/286ce00edd64/IANN_A_2059101_F0001_B.jpg

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