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延长 CAR-T 细胞持久性的制备策略

英文原题:Manufacturing strategies for prolonged CAR-T cell persistence.

查看英文原题

Manufacturing strategies for prolonged CAR-T cell persistence.

PubMed 2026/03/11(内容时间) Cytotherapy Q1 · IF 4.5(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞疗法已彻底改变血液系统恶性肿瘤的治疗,使对常规疗法难治的患者获得持久缓解。然而,输注的CAR-T 细胞持久性有限,原因包括T细胞耗竭及CAR-T 细胞丢失,这仍是实现持续疗效的主要障碍。近期研究显示,与常规CAR-T 产品相比,富集低分化记忆T细胞亚群的产品具有更好的长期持久性、更强的细胞毒性和更佳的临床结局。研究者已在制造流程的不同环节探索多种富集低分化记忆T细胞的策略,包括选择富含低分化记忆T细胞的细胞来源,以及通过调节信号通路、重塑表观遗传状态和调控代谢,延缓其向终末分化状态转变。本综述概述了当前及新兴的CAR-T 细胞制造策略,重点在于增强其长期持久性。仍需进一步研究,以确定不同临床情境下CAR-T 产品中已分化与低分化T细胞的最佳组成,从而推动产品个体化制造并最大限度提高疗效。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment of hematologic malignancies, achieving durable remission in patients who are refractory to conventional therapies.

However, the limited persistence of infused CAR-T cells, due to T-cell exhaustion and the loss of CAR-T cells, remains a major obstacle to sustained therapeutic efficacy. Recent studies have demonstrated that CAR-T cell products enriched for less-differentiated memory T cell subsets exhibit superior long-term persistence, greater cytotoxicity, and improved clinical outcomes compared with conventional CAR-T cell products.

To enrich for less-differentiated memory T cells, various strategies have been explored throughout the manufacturing process. These strategies include selecting cell sources enriched for less-differentiated memory T cells and delaying their differentiation into terminally differentiated states by regulating signaling pathways, remodeling epigenetics, and modulating metabolism. This review provides an overview of current and emerging manufacturing strategies for CAR-T cells, focusing on enhancing their prolonged persistence.

Further investigations are warranted to determine the optimal composition of differentiated and less-differentiated T cells in CAR-T cell products under the respective clinical conditions. This could facilitate the personalized manufacturing of CAR-T cell products with the ideal cell composition, thereby maximizing the efficacy of CAR-T cell therapy.

论文信息

作者
Shimasaki N
单位
Children's Cancer Center, Nagoya University Hospital, Nagoya, Aichi, Japan; Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Department of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan. Electronic address: shimasaki.noriko.t7@f.mail.nagoya-u.ac.jp.Japan
文献类型
综述
期刊
Cytotherapy2026 Aug
原文标识
PubMed 42250542 · DOI 10.1016/j.jcyt.2026.102778