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T 细胞受体(TCR)衍生疗法的优化策略和规则。

Strategies and rules for tuning TCR-derived therapy.

机构信息

State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Department of Immunology/Guangdong Provincial Key Laboratory of Proteomics, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, People's Republic of China.

出版信息

Expert Rev Mol Med. 2023 Dec 14;26:e4. doi: 10.1017/erm.2023.27.

Abstract

Manipulation of T cells has revolutionized cancer immunotherapy. Notably, the use of T cells carrying engineered T cell receptors (TCR-T) offers a favourable therapeutic pathway, particularly in the treatment of solid tumours. However, major challenges such as limited clinical response efficacy, off-target effects and tumour immunosuppressive microenvironment have hindered the clinical translation of this approach. In this review, we mainly want to guide TCR-T investigators on several major issues they face in the treatment of solid tumours after obtaining specific TCR sequences: (1) whether we have to undergo affinity maturation or not, and what parameter we should use as a criterion for being more effective. (2) What modifications can be added to counteract the tumour inhibitory microenvironment to make our specific T cells to be more effective and what is the safety profile of such modifications? (3) What are the new forms and possibilities for TCR-T cell therapy in the future?

摘要

T 细胞的操控革新了癌症免疫疗法。值得注意的是,携带工程化 T 细胞受体(TCR-T)的 T 细胞的应用提供了一种有利的治疗途径,特别是在治疗实体瘤方面。然而,诸如临床疗效有限、脱靶效应和肿瘤免疫抑制微环境等主要挑战阻碍了这种方法的临床转化。在这篇综述中,我们主要想为 TCR-T 研究人员提供一些指导,在获得特定 TCR 序列后,他们在治疗实体瘤时面临的几个主要问题:(1)我们是否必须进行亲和力成熟,如果要进行,应该使用什么参数作为更有效的标准。(2)可以添加哪些修饰来对抗肿瘤抑制微环境,以使我们的特异性 T 细胞更有效,以及此类修饰的安全性如何?(3)未来 TCR-T 细胞疗法有哪些新形式和可能性?

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e530/11062142/2bee07071d5f/S1462399423000273_fig1.jpg

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