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CAR-T 细胞效力:从结构元件到载体骨架组件

英文原题:CAR-T cell potency: from structural elements to vector backbone components.

查看英文原题

CAR-T cell potency: from structural elements to vector backbone components.

PubMed 2022/09/19(内容时间) Biomark Res Q1 · IF 14.6(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞疗法通过改造患者自身的T淋巴细胞使其能够识别并杀伤癌细胞,在部分血液系统恶性肿瘤的临床前和临床试验中取得了显著成功,目前已有六种FDA批准的CAR-T 产品上市。一旦装备了CAR构建体,T细胞便充当活体药物,以MHC非依赖的方式识别并清除靶肿瘤细胞。在本综述中,我们首先详细描述了CAR的所有结构模块,重点关注较新的发现。随后,我们指出了影响CAR表达的幕后因素,并综述了嵌入病毒载体骨架中的元件如何能够显著影响CAR的表达。

展开英文摘要原文

Chimeric antigen receptor (CAR) T cell therapy, in which a patient's own T lymphocytes are engineered to recognize and kill cancer cells, has achieved remarkable success in some hematological malignancies in preclinical and clinical trials, resulting in six FDA-approved CAR-T products currently available in the market.

Once equipped with a CAR construct, T cells act as living drugs and recognize and eliminate the target tumor cells in an MHC-independent manner. In this review, we first described all structural modular of CAR in detail, focusing on more recent findings.

We then pointed out behind-the-scene elements contributing to CAR expression and reviewed how CAR expression can be drastically affected by the elements embedded in the viral vector backbone.

论文信息

作者
Mazinani M、Rahbarizadeh F
第一作者单位
Department of Medical Biotechnology, Faculty of Medical Sciences, Tarbiat Modares University, P.O. Box 14115-111, Tehran, Iran.Iran
通讯作者单位
Department of Medical Biotechnology, Faculty of Medical Sciences, Tarbiat Modares University, P.O. Box 14115-111, Tehran, Iran. rahbarif@modares.ac.ir.Iran
文献类型
综述
期刊
Biomarker research2022 Sep 19
原文标识
PubMed 36123710 · DOI 10.1186/s40364-022-00417-w