Key Laboratory for Regenerative Medicine of Ministry of Education, Institute of Hematology, School of Medicine, Jinan University, Guangzhou, China.
Department of Pathology, School of Medicine, Jinan University, Guangzhou, China.
Front Immunol. 2023 Jan 27;14:1110325. doi: 10.3389/fimmu.2023.1110325. eCollection 2023.
Hematological malignancy develops and applies various mechanisms to induce immune escape, in part through an immunosuppressive microenvironment. Adenosine is an immunosuppressive metabolite produced at high levels within the tumor microenvironment (TME). Adenosine signaling through the A receptor expressed on immune cells, such as T cells, potently dampens immune responses. Extracellular adenosine generated by ectonucleoside triphosphate diphosphohydrolase-1 (CD39) and ecto-5'-nucleotidase (CD73) molecules is a newly recognized 'immune checkpoint mediator' and leads to the identification of immunosuppressive adenosine as an essential regulator in hematological malignancies. In this Review, we provide an overview of the detailed distribution and function of CD39 and CD73 ectoenzymes in the TME and the effects of CD39 and CD73 inhibition on preclinical hematological malignancy data, which provides insights into the potential clinical applications for immunotherapy.
血液系统恶性肿瘤通过多种机制诱导免疫逃逸,部分机制是通过免疫抑制微环境。腺苷是肿瘤微环境(TME)中高水平产生的免疫抑制代谢物。腺苷通过表达在免疫细胞(如 T 细胞)上的 A 受体信号传导,可有效抑制免疫反应。细胞外核苷酸三磷酸二磷酸水解酶-1(CD39)和外核苷酸 5′- 磷酸酶(CD73)分子产生的细胞外腺苷是一种新发现的“免疫检查点调节剂”,并将免疫抑制性腺苷鉴定为血液系统恶性肿瘤中的一个重要调节因子。在这篇综述中,我们概述了 CD39 和 CD73 胞外酶在 TME 中的详细分布和功能,以及 CD39 和 CD73 抑制对临床前血液系统恶性肿瘤数据的影响,为免疫治疗的潜在临床应用提供了思路。