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嵌合抗原受体 T 细胞疗法治疗实体瘤患者:需要汲取和摒弃的关键经验。

CAR T cell therapy for patients with solid tumours: key lessons to learn and unlearn.

机构信息

Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Pulmonary and Critical Care Division, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Nat Rev Clin Oncol. 2024 Jan;21(1):47-66. doi: 10.1038/s41571-023-00832-4. Epub 2023 Oct 30.

DOI:10.1038/s41571-023-00832-4
PMID:37904019
Abstract

Chimeric antigen receptor (CAR) T cells have been approved for use in patients with B cell malignancies or relapsed and/or refractory multiple myeloma, yet efficacy against most solid tumours remains elusive. The limited imaging and biopsy data from clinical trials in this setting continues to hinder understanding, necessitating a reliance on imperfect preclinical models. In this Perspective, I re-evaluate current data and suggest potential pathways towards greater success, drawing lessons from the few successful trials testing CAR T cells in patients with solid tumours and the clinical experience with tumour-infiltrating lymphocytes. The most promising approaches include the use of pluripotent stem cells, co-targeting multiple mechanisms of immune evasion, employing multiple co-stimulatory domains, and CAR ligand-targeting vaccines. An alternative strategy focused on administering multiple doses of short-lived CAR T cells in an attempt to pre-empt exhaustion and maintain a functional effector pool should also be considered.

摘要

嵌合抗原受体 (CAR) T 细胞已获准用于治疗 B 细胞恶性肿瘤或复发和/或难治性多发性骨髓瘤患者,但针对大多数实体瘤的疗效仍难以捉摸。该治疗领域临床试验的有限影像学和活检数据继续阻碍人们的理解,这需要依赖不完善的临床前模型。在本观点中,我重新评估了当前的数据,并从少数成功的在实体瘤患者中测试 CAR T 细胞的临床试验和肿瘤浸润淋巴细胞的临床经验中提出了一些可能的成功途径。最有前途的方法包括使用多能干细胞、共同靶向多种免疫逃逸机制、使用多个共刺激结构域以及 CAR 配体靶向疫苗。另一种策略侧重于多次给予短寿命的 CAR T 细胞,试图先发制人地阻止衰竭并维持功能性效应细胞池,也应加以考虑。

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Nat Med. 2023 Aug;29(8):2099-2109. doi: 10.1038/s41591-023-02452-y. Epub 2023 Jul 27.
3
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