| Literature DB >> 32030689 |
Jin-Qing Liu1, Aiyan Hu1,2, Jianmin Zhu1,2, Jianyu Yu1,3, Fatemeh Talebian1, Xue-Feng Bai4.
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.Entities:
Keywords: CD200; CD200 receptor; Cytotoxic T lymphocytes (CTLs); Dendritic cells (DCs); Immunotherapy; Myeloid derived suppressor cells (MDSCs); Regulatory T cells (Tregs); Tumor immunity; Tumor microenvironment; Tumor-associated macrophages (TAMs); Tumor-associated myeloid cells (TAMCs)
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Year: 2020 PMID: 32030689 PMCID: PMC7339106 DOI: 10.1007/978-3-030-35582-1_8
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622