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CD200-CD200R 通路在肿瘤免疫微环境调控及免疫治疗中的作用

CD200-CD200R Pathway in the Regulation of Tumor Immune Microenvironment and Immunotherapy.

机构信息

Department of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.

Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Adv Exp Med Biol. 2020;1223:155-165. doi: 10.1007/978-3-030-35582-1_8.

Abstract

Tumor-associated inflammation and immune responses are key components in the tumor microenvironment (TME) which regulate tumor growth, progression, and metastasis. Tumor-associated myeloid cells (TAMCs) are a group of cells that play multiple key roles including induction of tumor-associated inflammation/angiogenesis and regulation of tumor-specific T-cell responses. Thus, identification and characterization of key pathways that can regulate TAMCs are of critical importance for developing cancer immunotherapy. Recent studies suggest that CD200-CD200 receptor (CD200R) interaction may be important in regulating the TME via affecting TAMCs. In this chapter, we will give a brief overview of the CD200-CD200R axis, including the biology behind CD200-CD200R interaction and the role(s) it plays in tumor microenvironment and tumor growth, and activation/effector functions of T cells. We will also discuss CD200-CD200R's role as potential checkpoint molecules for cancer immunotherapy. Further investigation of the CD200-CD200R pathway will not only advance our understanding of tumor pathogenesis and immunity but also provide the rationale for CD200-CD200R-targeted immunotherapy of human cancer.

摘要

肿瘤相关炎症和免疫反应是肿瘤微环境(TME)的关键组成部分,调节肿瘤的生长、进展和转移。肿瘤相关髓系细胞(TAMCs)是一组细胞,它们发挥多种关键作用,包括诱导肿瘤相关炎症/血管生成和调节肿瘤特异性 T 细胞反应。因此,鉴定和表征可调节 TAMCs 的关键途径对于开发癌症免疫疗法至关重要。最近的研究表明,CD200-CD200 受体(CD200R)相互作用可能通过影响 TAMCs 在调节 TME 中起重要作用。在本章中,我们将简要概述 CD200-CD200R 轴,包括 CD200-CD200R 相互作用背后的生物学以及它在肿瘤微环境和肿瘤生长中的作用,以及 T 细胞的激活/效应功能。我们还将讨论 CD200-CD200R 作为癌症免疫治疗潜在检查点分子的作用。对 CD200-CD200R 途径的进一步研究不仅将推进我们对肿瘤发病机制和免疫的理解,而且为针对人类癌症的 CD200-CD200R 靶向免疫治疗提供了依据。

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