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CD19靶向嵌合抗原受体T细胞疗法后急性淋巴细胞白血病复发

Acute lymphoblastic leukemia relapse after CD19-targeted chimeric antigen receptor T cell therapy.

作者信息

Wang Jiasheng, Hu Yongxian, Huang He

机构信息

Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, Zhejiang, China.

Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, Zhejiang, China

出版信息

J Leukoc Biol. 2017 Dec;102(6):1347-1356. doi: 10.1189/jlb.5RU0817-315R. Epub 2017 Oct 10.

Abstract

CART19 therapy has revolutionized the treatment of CD19 acute lymphoblastic leukemia, demonstrating an unprecedented complete remission rate; however, as follow-up prolongs, a high relapse rate after CART19 therapy has emerged as one of the major problems. Relapse can be attributed to the loss of leukemic cell immunogenicity, diminished function and amount of CART19 cells, and the inhibitory bone marrow microenvironment. Although studies to prevent and treat relapse have begun, some encouraging results have demonstrated the possibility of decreasing the relapse rate. In this review, we focus on the possible mechanisms behind relapse. We will summarize and propose strategies to prevent and manage relapse on the basis of these potential mechanisms.

摘要

嵌合抗原受体T细胞(CART19)疗法彻底改变了CD19急性淋巴细胞白血病的治疗方式,展现出前所未有的完全缓解率;然而,随着随访时间的延长,CART19治疗后高复发率已成为主要问题之一。复发可归因于白血病细胞免疫原性丧失、CART19细胞功能和数量的减少以及抑制性骨髓微环境。尽管已经开始了预防和治疗复发的研究,一些令人鼓舞的结果已证明降低复发率的可能性。在本综述中,我们关注复发背后的可能机制。我们将基于这些潜在机制总结并提出预防和处理复发的策略。

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