Overview of LAG-3-Expressing, IL-10-Producing Regulatory T Cells

FOXP3型 白细胞介素2受体 生物 免疫系统 免疫学 周边公差 CD49b 肿瘤微环境 癌症研究 抗原提呈细胞 免疫耐受 细胞生物学 T细胞
作者
Keishi Fujio,Kazuhiko Yamamoto,Tomohisa Okamura
出处
期刊:Current Topics in Microbiology and Immunology 卷期号:: 29-45 被引量:36
标识
DOI:10.1007/82_2017_59
摘要

Regulatory T cells (Treg cells) play crucial roles in the induction of peripheral tolerance to self- and foreign-antigens. IL-10-producing regulatory T cells (IL-10-producing Treg cells) constitute a Treg cell subset characterized by the production of high amounts of IL-10, cytokine-mediated immunosuppressive capabilities, and independence of Foxp3 expression for their suppressive activity. In the past decade, identifying naturally occurring IL-10-producing Treg cells was difficult due to the lack of suitable surface markers. More recently, lymphocyte activation gene 3 (LAG-3) is a CD4 homologue that has been identified as a marker for IL-10-producing Treg cells. CD4+CD25−LAG3+ T cells produce large amounts of IL-10 and suppress colitis in a mouse model. These CD4+CD25−LAG3+ Treg cells also exhibit suppressive activity in murine models of lupus and humoral immunity in a TGF-β3-dependent manner. Moreover, the combined expression of LAG-3 and CD49b identifies IL-10-producing Treg cells in mice and humans more specifically. Recently, LAG-3 has gained more attention in the context of immune checkpoints because it believed to be related to T cell tolerance and exhausted T cells that infiltrate the tumor microenvironment. Tumors and the tumor microenvironment promote development of IL-10-producing Treg cells and foster tumor growth. This response might interfere with protective immune responses. Understanding LAG-3-expressing IL-10-producing Treg cells may contribute to the development of novel therapeutic strategies in immune-mediated diseases.
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