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利用无病毒技术拓展瞬时 CAR-T 治疗的边界

英文原题:Expanding the horizon of transient CAR T therapeutics using virus-free technology.

查看英文原题

Expanding the horizon of transient CAR T therapeutics using virus-free technology.

PubMed 2024/03/26(内容时间) Biotechnol Adv Q1 · IF 14.1(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞疗法多年来在对抗血液系统恶性肿瘤方面取得的非凡成功,已由市场上六款获FDA批准的产品所证明。CAR-T 疗法永远改变了我们对细胞免疫疗法的理解,因为该领域的当前研究甚至正在扩展到癌症领域之外,并取得了非常有前景的结果。迄今为止,基于病毒的策略一直被用于CAR-T 细胞制造。然而,这种方法存在相关局限性,需要在将该技术广泛推广至其他病理之前加以解决,并且为了优化当前的癌症治疗。目前正在探索多种方法来克服这些挑战,例如无病毒替代方案,此外还提供了开发瞬时CAR表达或体内T细胞修饰的可能性。在这篇综述中,我们旨在聚焦医学史上的一个关键节点,即正在发生重大观点转变的时刻。我们回顾了基于病毒的CAR-T 疗法当前取得的进展及其局限性,并讨论了无病毒CAR-T 策略的未来前景,以克服当前挑战并为包括癌症在内的多种病理实现可负担的免疫疗法。

展开英文摘要原文

The extraordinary success that chimeric antigen receptor (CAR) T cell therapies have shown over the years on fighting hematological malignancies is evidenced by the six FDA-approved products present on the market. CAR T treatments have forever changed the way we understand cellular immunotherapies, as current research in the topic is expanding even outside the field of cancer with very promising results. Until now, virus-based strategies have been used for CAR T cell manufacturing.

However, this methodology presents relevant limitations that need to be addressed prior to wide spreading this technology to other pathologies and in order to optimize current cancer treatments. Several approaches are being explored to overcome these challenges such as virus-free alternatives that additionally offer the possibility of developing transient CAR expression or in vivo T cell modification. In this review, we aim to spotlight a pivotal juncture in the history of medicine where a significant change in perspective is occurring.

We review the current progress made on viral-based CAR T therapies as well as their limitations and we discuss the future outlook of virus-free CAR T strategies to overcome current challenges and achieve affordable immunotherapies for a wide variety of pathologies, including cancer.

论文信息

作者
Enriquez-Rodriguez L、Attia N、Gallego I、Mashal M、Maldonado I、Puras G、Pedraz JL
第一作者单位
NanoBioCel Research Group, Laboratory of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Spain; Networking Research Centre of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Institute of Health Carlos III, Vitoria-Gasteiz, Spain; Bioaraba, NanoBioCel Research Group, Vitoria-Gasteiz, Spain.Spain
通讯作者单位
NanoBioCel Research Group, Laboratory of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Spain; Networking Research Centre of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Institute of Health Carlos III, Vitoria-Gasteiz, Spain; Bioaraba, NanoBioCel Research Group, Vitoria-Gasteiz, Spain. Electronic address: joseluis.pedraz@ehu.eus.Spain
文献类型
综述 · 非美国政府资助研究
期刊
Biotechnology advances2024 May-Jun
原文标识
PubMed 38537878 · DOI 10.1016/j.biotechadv.2024.108350