NHC Key Laboratory of Carcinogenesis and Hunan Key Laboratory of Cancer Metabolism, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410013, China; Cancer Research Institute, Basic School of Medicine, Central South University, Changsha, Hunan 410078, China.
NHC Key Laboratory of Carcinogenesis and Hunan Key Laboratory of Cancer Metabolism, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410013, China.
Biomed Pharmacother. 2022 Sep;153:113395. doi: 10.1016/j.biopha.2022.113395. Epub 2022 Jul 11.
Cluster of differentiation 38 (CD38) is a multifunctional extracellular enzyme on the cell surface with NADase and cyclase activities. CD38 is not only expressed in human immune cells, such as lymphocytes and plasma cells, but also is abnormally expressed in a variety of tumor cells, which is closely related to the occurrence and development of tumors. T cells are one of the important immune cells in the body. As NAD consuming enzymes, CD38, ART2, SIRT1 and PARP1 are closely related to the number and function of T cells. CD38 may also influence the activity of ART2, SIRT1 and PARP1 through the CD38-NAD axis to indirectly affect the number and function of T cells. Thus, CD38-NAD axis has a profound effect on T cell activity. In this paper, we reviewed the role and mechanism of CD38 CD4 T cells / CD38 CD8 T cells in cellular immunity and the effects of the CD38-NAD axis on T cell activity. We also summarized the relationship between the CD38 expression level on T cell surface and disease prediction and prognosis, the effects of anti-CD38 monoclonal antibodies on T cell activity and function, and the role of anti-CD38 chimeric antigen receptor (CAR) T cell therapy in tumor immunity. This will provide an important theoretical basis for a comprehensive understanding of the relationship between CD38 and T cells.
分化群 38(CD38)是细胞表面具有 NADase 和环化酶活性的多功能细胞外酶。CD38 不仅在人类免疫细胞(如淋巴细胞和浆细胞)中表达,而且在各种肿瘤细胞中异常表达,与肿瘤的发生和发展密切相关。T 细胞是体内重要的免疫细胞之一。作为 NAD 消耗酶,CD38、ART2、SIRT1 和 PARP1 与 T 细胞的数量和功能密切相关。CD38 还可以通过 CD38-NAD 轴影响 ART2、SIRT1 和 PARP1 的活性,从而间接影响 T 细胞的数量和功能。因此,CD38-NAD 轴对 T 细胞活性有深远的影响。本文综述了 CD38+CD4 T 细胞/CD38+CD8 T 细胞在细胞免疫中的作用及机制,以及 CD38-NAD 轴对 T 细胞活性的影响。还总结了 T 细胞表面 CD38 表达水平与疾病预测和预后的关系、抗 CD38 单克隆抗体对 T 细胞活性和功能的影响以及抗 CD38 嵌合抗原受体(CAR)T 细胞治疗在肿瘤免疫中的作用,为全面了解 CD38 与 T 细胞的关系提供了重要的理论依据。