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嵌合抗原受体T细胞疗法治疗自身免疫性疾病。

Chimeric antigen receptor T cell therapy for autoimmune disease.

作者信息

Chung James B, Brudno Jennifer N, Borie Dominic, Kochenderfer James N

机构信息

Kyverna Therapeutics Inc., Emeryville, CA, USA.

Surgery Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

出版信息

Nat Rev Immunol. 2024 Nov;24(11):830-845. doi: 10.1038/s41577-024-01035-3. Epub 2024 Jun 3.

Abstract

Infusion of T cells engineered to express chimeric antigen receptors (CARs) that target B cells has proven to be a successful treatment for B cell malignancies. This success inspired the development of CAR T cells to selectively deplete or modulate the aberrant immune responses that underlie autoimmune disease. Promising results are emerging from clinical trials of CAR T cells targeting the B cell protein CD19 in patients with B cell-driven autoimmune diseases. Further approaches are being designed to extend the application and improve safety of CAR T cell therapy in the setting of autoimmunity, including the use of chimeric autoantibody receptors to selectively deplete autoantigen-specific B cells and the use of regulatory T cells engineered to express antigen-specific CARs for targeted immune modulation. Here, we highlight important considerations, such as optimal target cell populations, CAR construct design, acceptable toxicities and potential for lasting immune reset, that will inform the eventual safe adoption of CAR T cell therapy for the treatment of autoimmune diseases.

摘要

输注经工程改造以表达靶向B细胞的嵌合抗原受体(CAR)的T细胞已被证明是治疗B细胞恶性肿瘤的成功方法。这一成功激发了CAR T细胞的研发,以选择性地消除或调节自身免疫性疾病所基于的异常免疫反应。针对B细胞驱动的自身免疫性疾病患者的靶向B细胞蛋白CD19的CAR T细胞临床试验正在产生有前景的结果。正在设计进一步的方法来扩展CAR T细胞疗法在自身免疫性疾病中的应用并提高其安全性,包括使用嵌合自身抗体受体来选择性消除自身抗原特异性B细胞,以及使用经工程改造以表达抗原特异性CAR的调节性T细胞进行靶向免疫调节。在此,我们强调了一些重要的考虑因素,如最佳靶细胞群体、CAR构建体设计、可接受的毒性以及持久免疫重置的可能性,这些因素将为最终安全采用CAR T细胞疗法治疗自身免疫性疾病提供参考。

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