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来自新型来源的 CAR 产品:肿瘤免疫治疗突破的新途径

英文原题:CAR products from novel sources: a new avenue for the breakthrough in cancer immunotherapy.

查看英文原题

CAR products from novel sources: a new avenue for the breakthrough in cancer immunotherapy.

PubMed 2024/04/11(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T 细胞疗法已改变癌症免疫治疗,但其应用仍局限于 B 细胞相关恶性肿瘤之外的领域,主要挑战包括临床疗效有限、毒性较高,以及自体细胞产品生产复杂。尽管人们不断努力改善 CAR-T 疗效,使用其他免疫细胞开发 CAR 细胞的兴趣日益增加。这些细胞具有多项优势,如不依赖主要组织相容性复合体(MHC)的作用、调节肿瘤微环境(TME)以及更强的组织浸润能力。目前正在探索多种 CAR 产品,包括不同 T 细胞亚型、先天免疫细胞、造血祖细胞,甚至外泌体来源的产品。这些 CAR 产品往往显示出更强的抗肿瘤疗效、更低的毒性和更优的肿瘤穿透能力。基于这些优势,许多临床试验正在评估新型 CAR 细胞的潜力。本综述全面审视这些新型 CAR 产品用于癌症治疗的优势、挑战和现有认识。

展开英文摘要原文

Chimeric antigen receptor (CAR) T cell therapy has transformed cancer immunotherapy.

However, significant challenges limit its application beyond B cell-driven malignancies, including limited clinical efficacy, high toxicity, and complex autologous cell product manufacturing. Despite efforts to improve CAR T cell therapy outcomes, there is a growing interest in utilizing alternative immune cells to develop CAR cells. These immune cells offer several advantages, such as major histocompatibility complex (MHC)-independent function, tumor microenvironment (TME) modulation, and increased tissue infiltration capabilities.

Currently, CAR products from various T cell subtypes, innate immune cells, hematopoietic progenitor cells, and even exosomes are being explored. These CAR products often show enhanced antitumor efficacy, diminished toxicity, and superior tumor penetration. With these benefits in mind, numerous clinical trials are underway to access the potential of these innovative CAR cells. This review aims to thoroughly examine the advantages, challenges, and existing insights on these new CAR products in cancer treatment.

论文信息

作者
Huang J、Yang Q、Wang W、Huang J
单位
Department of Hematology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.China
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2024
原文标识
PubMed 38665921 · DOI 10.3389/fimmu.2024.1378739