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

Adv Exp Med Biol

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

Published: February 2020

AI Article Synopsis

  • * The CD200-CD200 receptor (CD200R) interaction is highlighted as a critical pathway that regulates TAMCs and the TME, potentially affecting tumor progression and T-cell responses.
  • * Understanding the CD200-CD200R axis could lead to important breakthroughs in cancer immunotherapy by offering new strategies to target these pathways for improved treatment outcomes.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7339106PMC
http://dx.doi.org/10.1007/978-3-030-35582-1_8DOI Listing

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