Identification and characterization of latency-associated peptide-expressing γδ T cells

潜伏期相关肽表达γδT细胞的鉴定和表征

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作者:Rafael M Rezende, Andre P da Cunha, Chantal Kuhn, Stephen Rubino, Hanane M'Hamdi, Galina Gabriely, Tyler Vandeventer, Shirong Liu, Ron Cialic, Natalia Pinheiro-Rosa, Rafael P Oliveira, Jellert T Gaublomme, Nikolaus Obholzer, James Kozubek, Nathalie Pochet, Ana M C Faria, Howard L Weiner

Abstract

γδ T cells are a subset of lymphocytes specialized in protecting the host against pathogens and tumours. Here we describe a subset of regulatory γδ T cells that express the latency-associated peptide (LAP), a membrane-bound TGF-β1. Thymic CD27+IFN-γ+CCR9+α4β7+TCRγδ+ cells migrate to the periphery, particularly to Peyer's patches and small intestine lamina propria, where they upregulate LAP, downregulate IFN-γ via ATF-3 expression and acquire a regulatory phenotype. TCRγδ+LAP+ cells express antigen presentation molecules and function as antigen presenting cells that induce CD4+Foxp3+ regulatory T cells, although TCRγδ+LAP+ cells do not themselves express Foxp3. Identification of TCRγδ+LAP+ regulatory cells provides an avenue for understanding immune regulation and biologic processes linked to intestinal function and disease.

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