Beyond Oncology: Exploring the Expanding Role of CAR T Cell Therapy in Autoimmune and Infectious Diseases-A Systematic Review.

Kawther Zaher, Jehan Alrahimi
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Abstract

Background: Chimeric antigen receptor (CAR) T cell therapy has revolutionized the treatment of select hematologic malignancies and is increasingly being explored for non-oncological indications, including autoimmune diseases and persistent infectious diseases. This systematic review synthesized current evidence on CAR T cell and CAR-Treg approaches beyond oncology, with emphasis on therapeutic targets, translational and clinical outcomes, safety, and implementation barriers. Methods: The review followed PRISMA 2020 guidelines. PubMed/MEDLINE, Scopus, Web of Science, Cochrane Library, ClinicalTrials.gov, and major trial registries were searched for studies published from 1 January 2010 to 31 March 2026. Eligible studies included clinical, preclinical, and translational investigations of CAR T cell or CAR-Treg strategies in autoimmune or infectious diseases. Results: Because of heterogeneity in disease indications, CAR constructs, endpoints, and study designs, findings were synthesized descriptively. The strongest early clinical signals were observed with B cell-directed CAR T cell therapy for severe, refractory autoimmune diseases, particularly systemic lupus erythematosus, systemic sclerosis, and inflammatory myopathies. Infectious disease applications, mainly HIV and hepatitis B, showed preliminary safety, persistence, and partial antiviral activity, but durable pathogen eradication remains unproven. Conclusion: Overall, CAR T cell therapy beyond oncology is promising but remains preliminary, requiring standardized reporting, long-term safety monitoring, scalable manufacturing, and carefully defined risk-benefit thresholds. Human clinical evidence was interpreted separately from preclinical and mechanistic evidence, and clinical conclusions were based primarily on human studies.

超越肿瘤学:探索CAR - T细胞治疗在自身免疫性和感染性疾病中的扩展作用-系统综述。
背景:嵌合抗原受体(CAR) T细胞疗法已经彻底改变了某些血液系统恶性肿瘤的治疗,并且越来越多地用于非肿瘤适应症的探索,包括自身免疫性疾病和持续性感染性疾病。本系统综述综合了目前肿瘤以外CAR-T细胞和CAR- treg方法的证据,重点是治疗靶点、转化和临床结果、安全性和实施障碍。方法:按照PRISMA 2020指南进行综述。检索了PubMed/MEDLINE、Scopus、Web of Science、Cochrane Library、ClinicalTrials.gov和主要试验注册库,检索了2010年1月1日至2026年3月31日发表的研究。符合条件的研究包括CAR-T细胞或CAR- treg策略在自身免疫性或感染性疾病中的临床、临床前和转化性研究。结果:由于疾病适应症、CAR结构、终点和研究设计的异质性,研究结果是描述性的。B细胞导向的CAR - T细胞治疗对严重的、难治性自身免疫性疾病,特别是系统性红斑狼疮、系统性硬化症和炎症性肌病,具有最强的早期临床信号。传染病应用,主要是HIV和乙型肝炎,显示出初步的安全性、持久性和部分抗病毒活性,但持久的病原体根除仍未得到证实。结论:总的来说,CAR - T细胞治疗超越肿瘤是有希望的,但仍处于初步阶段,需要标准化的报告、长期的安全性监测、可扩展的生产和仔细定义的风险-收益阈值。人类临床证据与临床前证据和机械证据分开解释,临床结论主要基于人类研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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