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细胞因子装甲 CAR-T 细胞研发进展

英文原题:Progress in the development of cytokine armoured CAR T cells.

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Progress in the development of cytokine armoured CAR T cells.

PubMed 2026/03/06(内容时间) Nat Rev Immunol Q1 · IF 47.1(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T 细胞工程已从第一代构建体发展至复杂的第四代装甲型 CAR-T 细胞。这些先进细胞经工程化改造,可在表达 CAR 的同时共表达细胞因子、趋化因子或其他免疫调节因子,旨在增强 CAR-T 细胞在肿瘤微环境中的疗效、安全性和持续性。尤其是逆转免疫抑制的潜力,有望使其用于迫切需要新治疗选择的实体瘤。本文综述细胞因子增强型 CAR-T 细胞的临床与临床前研究发现,并讨论通过条件性细胞因子分泌降低全身毒性的策略。

展开英文摘要原文

The engineering of chimeric antigen receptor (CAR) T cells has evolved from first-generation constructs to sophisticated armoured CAR T cells of the fourth generation.

These advanced cellular constructs are engineered to co-express cytokines, chemokines or other immunomodulatory factors alongside CARs, aiming to enhance the efficacy, safety and persistence of CAR T cells within the tumour microenvironment. In particular, the potential for reversion of immunosuppression may allow for the treatment of solid tumours, which are in need of new therapeutic options.

Here, we explore clinical and preclinical findings with cytokine-enhanced CAR T cells and discuss strategies for conditional cytokine secretion to mitigate systemic toxicity.

论文信息

作者
Prasad K、Cross RS、Jenkins MR
第一作者单位
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.Australia
通讯作者单位
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia. Jenkins.m@wehi.edu.au.Australia
文献类型
综述
期刊
Nature reviews. Immunology2026 Jul
原文标识
PubMed 41792262 · DOI 10.1038/s41577-026-01280-8