Liang Zhenguo, Xie Hui, Wu Dongze
Department of Rheumatology and Immunology, The Fifth Affiliated Hospital, Sun Yat-Sen University, Zhuhai, Guangdong, China.
Department of Clinical Research and Development, Antengene Corporation, Shanghai, China.
Front Immunol. 2025 Apr 7;16:1520063. doi: 10.3389/fimmu.2025.1520063. eCollection 2025.
Despite the advancements in targeted biologic therapy for immune-mediated inflammatory diseases (IMIDs), significant challenges persist, including challenges in drug maintenance, primary and secondary non-responses, and adverse effects. Recent data have strengthened the evidence supporting stem cell therapy as an experimental salvage therapy into a standard treatment option. Recent preclinical and clinical studies suggested that chimeric antigen receptor T cell (CAR-T) therapy, which depleting tissue and bone marrow B cells, may lead to improvement, even inducing long-lasting remissions for patients with IMIDs. In this review, we address the unmet needs of targeted biologic therapy, delineate the critical differences between stem cell transplantation and CAR-T therapy, evaluate the current status of CAR-T therapy for IMIDs and explore its potential and existing limitations.
尽管免疫介导的炎症性疾病(IMIDs)的靶向生物疗法取得了进展,但重大挑战依然存在,包括药物维持、原发性和继发性无反应以及不良反应方面的挑战。最近的数据进一步证明了干细胞疗法作为一种实验性挽救疗法成为标准治疗选择的证据。最近的临床前和临床研究表明,嵌合抗原受体T细胞(CAR-T)疗法可消耗组织和骨髓中的B细胞,可能会使IMIDs患者病情改善,甚至实现长期缓解。在这篇综述中,我们阐述了靶向生物疗法未满足的需求,描述了干细胞移植和CAR-T疗法之间的关键差异,评估了IMIDs的CAR-T疗法的现状,并探讨了其潜力和现有局限性。