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Bispecific antibodies in cancer immunotherapy.
Current Opinion in Biotechnology ( IF 7.1 ) Pub Date : 2019-12-13 , DOI: 10.1016/j.copbio.2019.11.020
Christoph Rader 1
Affiliation  

Among antibody-based cancer therapies, bispecific antibodies (biAbs) have gained momentum in preclinical and clinical investigations following the regulatory approvals of the trailblazing T-cell engaging biAb (T-biAb) blinatumomab. Discussed herein are recent strategies that aim at boosting the potency and mitigating the toxicity of T-biAbs, broadening their therapeutic utility from hematologic to solid malignancies, and generating T-biAbs in situ. In cancer immunotherapy, T-biAbs are facing fierce competition with chimeric antigen receptor T cells (CAR-Ts), a battle for clinical and commercial viability that will be closely watched. However, innovative combinations of T-biAbs and CAR-Ts have also transpired. NK-cell engaging biAbs (NK-biAbs) are reemerging as an alternative that addresses liabilities of T-biAbs. Beyond NK-biAbs, other biAbs designed to recruit cellular and molecular components of the innate immune system will be covered in this reflection on new tools, technologies, and targets.

中文翻译:

癌症免疫治疗中的双特异性抗体。

在基于抗体的癌症疗法中,双特异性抗体 (biAb) 在开拓性 T 细胞结合 biAb (T-biAb) blinatumomab 获得监管批准后,在临床前和临床研究中获得了动力。本文讨论的是最近的策略,旨在提高 T-biAb 的效力并减轻其毒性,将其治疗效用从血液学扩展到实体恶性肿瘤,并原位生成 T-biAb。在癌症免疫治疗中,T-biAb 面临着与嵌合抗原受体 T 细胞 (CAR-T) 的激烈竞争,这是一场备受关注的临床和商业可行性之战。然而,T-biAbs 和 CAR-Ts 的创新组合也出现了。与 NK 细胞结合的双抗体 (NK-biAb) 正在重新出现,作为解决 T-biAb 缺陷的替代方案。除了 NK-biAbs,
更新日期:2020-04-20
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