Department of Medicine, Division of Hematology and Oncology, University of Virginia Cancer Center, Charlottesville, VA, USA.
TransTarget, Inc., Sunnyvale, CA, USA.
Ann Med. 2022 Dec;54(1):1047-1057. doi: 10.1080/07853890.2022.2059101.
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.
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。