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超越肿瘤的 CAR-T 治疗:一种活体药物的演化

英文原题:CAR T therapy beyond cancer: the evolution of a living drug.

查看英文原题

CAR T therapy beyond cancer: the evolution of a living drug.

PubMed 2023/07/26(内容时间) Nature Q1 · IF 56.1(JCR 2025)

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中文摘要

将患者自身的T细胞工程化以选择性靶向并清除肿瘤细胞,已治愈了无法治疗的血系统恶性肿瘤患者。这些结果激励了整个肿瘤学领域应用嵌合抗原受体(CAR)T疗法。然而,来自临床和临床前研究的证据强调了CAR-T 疗法在肿瘤学之外治疗自身免疫、慢性感染、心脏纤维化、衰老相关疾病及其他病症的潜力。同时,新技术和平台的部署为CAR-T 疗法应用于非恶性病变提供了进一步的机会。在此,我们综述了CAR-T 疗法背后的原理、肿瘤学中当前面临的挑战、非恶性疾病初步报告的概要,以及相关新兴技术的讨论。我们考察了该疗法在广泛背景下的潜在应用。最后,我们强调了关于特异性和安全性的担忧,并概述了CAR-T 疗法超越癌症的前进路径。

展开英文摘要原文

Engineering a patient's own T cells to selectively target and eliminate tumour cells has cured patients with untreatable haematologic cancers. These results have energized the field to apply chimaeric antigen receptor (CAR) T therapy throughout oncology.

However, evidence from clinical and preclinical studies underscores the potential of CAR T therapy beyond oncology in treating autoimmunity, chronic infections, cardiac fibrosis, senescence-associated disease and other conditions. Concurrently, the deployment of new technologies and platforms provides further opportunity for the application of CAR T therapy to noncancerous pathologies.

Here we review the rationale behind CAR T therapy, current challenges faced in oncology, a synopsis of preliminary reports in noncancerous diseases, and a discussion of relevant emerging technologies.

We examine potential applications for this therapy in a wide range of contexts. Last, we highlight concerns regarding specificity and safety and outline the path forward for CAR T therapy beyond cancer.

论文信息

作者
Baker DJ、Arany Z、Baur JA、Epstein JA、June CH
第一作者单位
Center for Cellular Immunotherapies, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA. bakerda@pennmedicine.upenn.edu.United States
通讯作者单位
Center for Cellular Immunotherapies, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA. cjune@upenn.edu.United States
文献类型
综述 · 非美国政府资助研究 · 美国 NIH 资助研究
期刊
Nature2023 Jul
原文标识
PubMed 37495877 · DOI 10.1038/s41586-023-06243-w