靶向巨噬细胞的癌症治疗策略
Macrophage-directed therapeutic strategies in cancer.
肿瘤相关巨噬细胞(TAMs)是肿瘤微环境的主要组成部分,具有显著的功能可塑性,根据所处的微环境信号,既可表现为促进肿瘤进展的免疫抑制细胞,也可表现为支持抗肿瘤免疫的免疫刺激细胞。
英文原题:T cell receptor therapeutics: immunological targeting of the intracellular cancer proteome.
T细胞受体(TCR)复合物是一种天然存在的抗原传感器,能够检测、放大并协调针对源自细胞表面和细胞内蛋白表位的细胞免疫应答。
T 细胞受体(TCR)复合物是一种天然存在的抗原传感器,能够检测、放大并协调针对源自细胞表面和细胞内蛋白表位的细胞免疫应答。因此,TCR 能够靶向癌细胞选择性表达的蛋白,包括新抗原、癌-睾丸抗原和病毒癌蛋白。正因如此,TCR 为新兴的一类肿瘤治疗药物奠定了基础。本文中,我们综述了当前利用 TCR 和 TCR 样分子进行癌症治疗的格局。这包括表达内源性或工程化 TCR 的 T 细胞的过继性细胞转移、TCR 双特异性衔接分子以及针对人白细胞抗原(HLA)结合肽的特异性抗体(TCR 模拟物)。我们讨论了与这些治疗药物临床开发相关的独特复杂性,如 HLA 限制性、TCR 获取、效力评估以及交叉反应的可能性。此外,我们重点介绍了确立基于 TCR 的疗法(包括TIL(肿瘤浸润淋巴细胞)抗肿瘤潜力的新兴临床数据,用于治疗多种人类恶性肿瘤。最后,我们探讨了 TCR 治疗药物的未来,包括新兴的基因组编辑方法以安全增强效力,以及简化患者识别的策略。
The T cell receptor (TCR) complex is a naturally occurring antigen sensor that detects, amplifies and coordinates cellular immune responses to epitopes derived from cell surface and intracellular proteins. Thus, TCRs enable the targeting of proteins selectively expressed by cancer cells, including neoantigens, cancer germline antigens and viral oncoproteins. As such, TCRs have provided the basis for an emerging class of oncology therapeutics. Herein, we review the current cancer treatment landscape using TCRs and TCR-like molecules. This includes adoptive cell transfer of T cells expressing endogenous or engineered TCRs, TCR bispecific engagers and antibodies specific for human leukocyte antigen (HLA)-bound peptides (TCR mimics). We discuss the unique complexities associated with the clinical development of these therapeutics, such as HLA restriction, TCR retrieval, potency assessment and the potential for cross-reactivity. In addition, we highlight emerging clinical data that establish the antitumour potential of TCR-based therapies, including tumour-infiltrating lymphocytes, for the treatment of diverse human malignancies. Finally, we explore the future of TCR therapeutics, including emerging genome editing methods to safely enhance potency and strategies to streamline patient identification.
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