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CAR-T 细胞应用于实体瘤

英文原题:Chimeric antigen receptor T cells applied to solid tumors.

查看英文原题

Chimeric antigen receptor T cells applied to solid tumors.

PubMed 2022/10/31(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

CAR-T 细胞疗法是一种新型肿瘤免疫疗法,可使自体T细胞表达合成受体,特异性识别肿瘤相关表面抗原,进而发挥抗肿瘤作用,克服癌症耐药、转移和复发。CAR-T 细胞虽已成功清除血液系统恶性肿瘤,但由于免疫抑制性肿瘤微环境以及缺乏肿瘤特异性靶抗原等障碍,其用于实体瘤的应用尚未实现。本文介绍实体瘤CAR-T 细胞疗法开发进展,简要总结其挑战,以及克服这些障碍的新型工程和药物干预措施。展望未来,讨论预计未来几年进入临床研究的最新工作,包括基于CRISPR筛选的CAR改造,以及由祖细胞样T细胞制备CAR-T 细胞。总之,本文可能启发研究者和临床医生开发可在实体瘤中临床应用的CAR-T 细胞治疗策略。

展开英文摘要原文

Chimeric antigen receptor T cell (CAR-T) therapy is novel tumor immunotherapy that enables autologous T to express synthetic receptors to specifically recognize the surface tumor-associated antigens for exerting subsequent antitumor effects, and eliminating the resistance, metastases and recurrence of cancer. Although CAR T cells have exhibited success in eradicating hematologic malignancies, their applications to solid tumors has not yet been achieved due to obstacles such as the immune-suppressor tumor microenvironment and lack of tumor specific target antigens.

In this review, we presented advancements in the development of CAR T cell therapy in solid tumors, and offered a brief summary of the challenges, as well as novel engineering and pharmaceutical interventions to overcome these barriers.

Looking forward, we discussed the latest studies which are expected to reach the clinicals in the next few years, including CRISPR screens-based CAR modification and CAR T cells driven from progenitor-like T cells. Collectively, this review may inspire researchers and clinicians to develop clinical available strategies of CAR T cell therapies in solid tumor.

论文信息

作者
Zhou Z、Tao C、Li J、Tang JC、Chan AS、Zhou Y
第一作者单位
School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.Australia
通讯作者单位
School of Biomedical Engineering, Sun Yat-sen University, Guangzhou, Guangdong, China.China
文献类型
综述
期刊
Frontiers in immunology2022
原文标识
PubMed 36389701 · DOI 10.3389/fimmu.2022.984864