Bao Yu-Tong, Lv Meng, Huang Xiao-Jun, Zhao Xiang-Yu
Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Cell and Gene Therapy for Hematologic Malignancies, Beijing, China.
Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Cell and Gene Therapy for Hematologic Malignancies, Beijing, China; Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Cancer Lett. 2025 Aug 28;626:217771. doi: 10.1016/j.canlet.2025.217771. Epub 2025 May 2.
Chimeric antigen receptor (CAR) T cell therapy has emerged as a groundbreaking treatment for hematological malignancies, particularly B-cell malignancies. However, its high risk of relapse and low efficacy in malignancies such as chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML) have limited its clinical utility. The expansion, infiltration and persistence of CAR-T cells are key determinants of their efficacy. It has been recognized that limited expansion and lack of persistence are major contributors to non-remission and early relapse, highlighting the need to elucidate their mechanisms and countermeasures. In this review, we described features of CAR-T cell expansion and persistence in various hematogenic malignancies and solid tumors. Then, current knowledge on the mechanisms underlying deficiency in CAR-T cell expansion and persistence is presented, focusing on the intrinsic deficiency of CAR-T cells as well as their interaction with the systemic and local immune environment. Finally, we summarize approaches to enhance CAR-T cell expansion and persistence by improving CAR-T cell quality and overcoming the immunosuppressive environment.
嵌合抗原受体(CAR)T细胞疗法已成为治疗血液系统恶性肿瘤,尤其是B细胞恶性肿瘤的开创性疗法。然而,其在慢性淋巴细胞白血病(CLL)和急性髓系白血病(AML)等恶性肿瘤中复发风险高且疗效低,限制了其临床应用。CAR-T细胞的扩增、浸润和持久性是其疗效的关键决定因素。人们已经认识到,扩增受限和缺乏持久性是导致未缓解和早期复发的主要因素,这凸显了阐明其机制和应对措施的必要性。在这篇综述中,我们描述了CAR-T细胞在各种血液系统恶性肿瘤和实体瘤中的扩增和持久性特征。然后,介绍了目前关于CAR-T细胞扩增和持久性不足的潜在机制的知识,重点关注CAR-T细胞的内在缺陷及其与全身和局部免疫环境的相互作用。最后,我们总结了通过提高CAR-T细胞质量和克服免疫抑制环境来增强CAR-T细胞扩增和持久性的方法。