← 返回

克服癌细胞对 CAR-T 细胞杀伤的内在耐药

英文原题:Overcoming Intrinsic Resistance of Cancer Cells to CAR T-Cell Killing.

查看英文原题

Overcoming Intrinsic Resistance of Cancer Cells to CAR T-Cell Killing.

PubMed 2021/07/12(内容时间) Clin Cancer Res Q1 · IF 10.9(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

近几年,嵌合抗原受体(CAR)T 细胞疗法已成为标准治疗失败癌症的一种有前景疗法,并已获批用于 B 细胞白血病和淋巴瘤等血液癌症。尽管取得这些进展,相当比例患者仍对 CAR-T 治疗产生原发性或继发性耐药。本文综述 CAR-T 细胞清除靶细胞的机制,以及癌细胞可能对这种杀伤不敏感的情形(本文称为内在耐药)。近期研究提示,通过死亡受体信号激活细胞凋亡,是 CAR-T 体内细胞毒作用的重要机制。确实,凋亡机制异常的癌细胞可能对 CAR-T 杀伤不敏感。这种癌细胞对 CAR-T 杀伤的内在耐药,可能导致相当一部分治疗失败。最后,本文讨论可能用于克服此类耐药、增强 CAR-T 疗效的策略。

展开英文摘要原文

In the past few years, chimeric antigen receptor (CAR) T-cell therapy has emerged as a promising treatment for cancers that failed standard treatments. Such therapies have already been approved in several blood cancers, such as B-cell leukemia and lymphoma. Despite this progress, a significant proportion of patients experience primary or secondary resistance to CAR T-cell therapy.

Here, we review the mechanisms by which CAR T cells eliminate their target and how cancer cells may be insensitive to such killing (here referred to as intrinsic resistance).

Recent studies suggest that the activation of apoptosis through death receptor signaling is responsible for a major part of CAR T-cell cytotoxicity in vivo Indeed, cancer cells harboring aberrant apoptotic machinery may be insensitive to CAR T-cell killing. This intrinsic resistance of cancer cells to CAR T-cell killing could be responsible for a significant portion of treatment failure.

Finally, we discuss strategies that may be envisioned to overcome such resistance to enhance CAR T-cell efficacy.

论文信息

作者
Lemoine J、Ruella M、Houot R
第一作者单位
AP-HP, Department of Hematology, Université de Paris, Paris, France.France
通讯作者单位
Department of Hematology, CHU de Rennes, Université de Rennes, INSERM U1236, Rennes, France. roch.houot@chu-rennes.fr.France
文献类型
综述
期刊
Clinical cancer research : an official journal of the American Association for Cancer Research2021 Dec 1
原文标识
PubMed 34253582 · DOI 10.1158/1078-0432.CCR-21-1559