From concept to cure: The evolution of CAR-T cell therapy.

IF 12.1 1区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Molecular Therapy Pub Date : 2025-05-07 Epub Date: 2025-03-10 DOI:10.1016/j.ymthe.2025.03.005
Kisha K Patel, Mito Tariveranmoshabad, Siddhant Kadu, Nour Shobaki, Carl June
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引用次数: 0

Abstract

Chimeric antigen receptor (CAR)-T cell therapy has revolutionized cancer immunotherapy in the 21st century, providing innovative solutions and life-saving therapies for previously untreatable diseases. This approach has shown remarkable success in treating various hematological malignancies and is now expanding into clinical trials for solid tumors, such as prostate cancer and glioblastoma, as well as infectious and autoimmune diseases. CAR-T cell therapy involves harvesting a patient's T cells, genetically engineering them with viral vectors to express CARs targeting specific antigens and reinfusing the modified cells into the patient. These CAR-T cells function independently of major histocompatibility complex (MHC) antigen presentation, selectively identifying and eliminating target cells. This review highlights the key milestones in CAR-T cell evolution, from its invention to its clinical applications. It outlines the historical timeline leading to the invention of CAR-T cells, discusses the major achievements that have transformed them into a breakthrough therapy, and addresses remaining challenges, including high manufacturing costs, limited accessibility, and toxicity issues such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. Additionally, the review explores future directions and advances in the field, such as developing next-generation CAR-T cells aiming to maximize efficacy, minimize toxicity, and broaden therapeutic applications.

从概念到治愈:CAR-T细胞疗法的演变。
嵌合抗原受体(CAR)-T细胞疗法在21世纪彻底改变了癌症免疫疗法,为以前无法治愈的疾病提供了创新的解决方案和挽救生命的疗法。这种方法在治疗各种血液恶性肿瘤方面取得了显著的成功,现在正在扩展到实体肿瘤的临床试验,如前列腺癌和胶质母细胞瘤,以及感染性和自身免疫性疾病。CAR-T细胞疗法包括收集患者的T细胞,用病毒载体对其进行基因改造,以表达针对特定抗原的CAR-T细胞,然后将修饰后的细胞重新注入患者体内。这些CAR-T细胞独立于主要组织相容性复合体(MHC)抗原呈递,选择性地识别和消除靶细胞。本文回顾了CAR-T细胞从发明到临床应用的发展历程。它概述了导致CAR-T细胞发明的历史时间线,讨论了将其转化为突破性疗法的主要成就,并解决了仍然存在的挑战,包括高制造成本,有限的可及性和毒性问题,如细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性综合征(ICANS)。此外,该综述还探讨了该领域的未来方向和进展,例如开发下一代CAR-T细胞,旨在最大限度地提高疗效,减少毒性,扩大治疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Therapy
Molecular Therapy 医学-生物工程与应用微生物
CiteScore
19.20
自引率
3.20%
发文量
357
审稿时长
3 months
期刊介绍: Molecular Therapy is the leading journal for research in gene transfer, vector development, stem cell manipulation, and therapeutic interventions. It covers a broad spectrum of topics including genetic and acquired disease correction, vaccine development, pre-clinical validation, safety/efficacy studies, and clinical trials. With a focus on advancing genetics, medicine, and biotechnology, Molecular Therapy publishes peer-reviewed research, reviews, and commentaries to showcase the latest advancements in the field. With an impressive impact factor of 12.4 in 2022, it continues to attract top-tier contributions.
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