决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Bispecific antibodies for the treatment of neuroblastoma.
双特异性抗体(BsAb)是新一代基于抗体的疗法,可将人工特异性赋予多克隆 T 细胞或放射性半抗原。
双特异性抗体(BsAb)是新一代抗体类疗法,可赋予多克隆T细胞或放射性半抗原人工特异性。这些药物已成功用于治疗血液系统恶性肿瘤,目前也在实体瘤(包括高危神经母细胞瘤〔HRNB〕)中开展临床研究。旨在募集T细胞或提高放疗治疗指数的BsAb,有望通过缩小大体积肿瘤、更有效清除微转移并预防复发,显著改善HRNB患者的长期生存。BsAb还可用于武装T细胞,产生类似CAR-T细胞的产品,且安全性可能更好。审慎且务实地将这些疗法整合进标准治疗,有望使全球更多患者受益。本文介绍BsAb用于HRNB的近30年发展历程,讨论所有相关BsAb的优势和局限,包括T细胞连接器和放射免疫治疗药物,并强调结构设计及结构域间距对抗肿瘤疗效的重要性。
Bispecific antibodies (BsAb) are a new generation of antibody-based therapy, conveying artificial specificity to polyclonal T cells or radiohaptens. These drugs have been successfully implemented to cure hematologic malignancies and are under clinical investigation for solid tumors including HRNB. BsAbs designed to engage T cells or increase the therapeutic index of radiotherapy hold the potential to significantly improve the long-term survival of HRNB patients by shrinking bulky tumors and more effectively eliminating micrometastases and preventing relapse. BsAbs can also be used to arm T cells, yielding a product analogous to CAR T cells, possibly with an improved safety profile. A thoughtful and realistic integration of these therapies into the standard of care should benefit more patients worldwide. Here we describe the history of development of BsAbs for HRNB, which dates back almost three decades. We discuss the merits and pitfalls of all relevant BsAbs, including T cell-engagers and agents used for radioimmunotherapy, highlighting the importance of structural design and interdomain spacing for anti-tumor efficacy.
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