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T 细胞衰老和嵌合抗原受体 T 细胞耗竭在血液恶性肿瘤中的作用。

T cell senescence and CAR-T cell exhaustion in hematological malignancies.

机构信息

Key Laboratory for Regenerative Medicine of Ministry of Education, Institute of Hematology, School of Medicine, Jinan University, Guangzhou, 510632, China.

Department of Anatomy and Molecular Embryology, Institute of Anatomy, Ruhr-University Bochum, 44801, Bochum, Germany.

出版信息

J Hematol Oncol. 2018 Jul 4;11(1):91. doi: 10.1186/s13045-018-0629-x.

Abstract

T cell senescence has been recognized to play an immunosuppressive role in the aging population and cancer patients. Strategies dedicated to preventing or reversing replicative and premature T cell senescence are required to increase the lifespan of human beings and to reduce the morbidity from cancer. In addition, overcoming the T cell terminal differentiation or senescence from lymphoma and leukemia patients is a promising approach to enhance the effectiveness of adoptive cellular immunotherapy (ACT). Chimeric antigen receptor T (CAR-T) cell and T cell receptor-engineered T (TCR-T) cell therapy highly rely on functionally active T cells. However, the mechanisms which drive T cell senescence remain unclear and controversial. In this review, we describe recent progress for restoration of T cell homeostasis from age-related senescence as well as recovery of T cell activation in hematological malignancies.

摘要

T 细胞衰老已被认为在老年人群体和癌症患者中发挥免疫抑制作用。需要专门的策略来预防或逆转复制性和过早的 T 细胞衰老,以延长人类的寿命并降低癌症的发病率。此外,克服淋巴瘤和白血病患者的 T 细胞终末分化或衰老,是增强过继细胞免疫治疗(ACT)效果的一种有前途的方法。嵌合抗原受体 T(CAR-T)细胞和 T 细胞受体工程化 T(TCR-T)细胞治疗高度依赖于功能活跃的 T 细胞。然而,导致 T 细胞衰老的机制尚不清楚且存在争议。在这篇综述中,我们描述了从与年龄相关的衰老中恢复 T 细胞动态平衡以及恢复血液恶性肿瘤中 T 细胞激活的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62e6/6032767/e2fababa63e1/13045_2018_629_Fig1_HTML.jpg

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