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

Rezende, RM (author)
da Cunha, AP (author)
Kuhn, C (author)
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Rubino, S (author)
M'Hamdi, H (author)
Gabriely, G (author)
Vandeventer, T (author)
Liu, SR (author)
Cialic, R (author)
Pinheiro-Rosa, N (author)
Oliveira, RP (author)
Gaublomme, JT (author)
Obholzer, N (author)
Kozubek, J (author)
Pochet, N (author)
Faria, AMC (author)
Weiner, HL (author)
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2015-12-08
2015
English.
In: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 6, s. 8726-
  • Journal article (peer-reviewed)
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  • 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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