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Identification and characterization of latency-associated peptide-expressing γδT cells

  • 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

Research output: Contribution to journal › Article › peer-review

Abstract

γδT cells are a subset of lymphocytes specialized in protecting the host against pathogens and tumours. Here we describe a subset of regulatory γδT cells that express the latency-associated peptide (LAP), a membrane-bound TGF-β1. Thymic CD27+IFN-γ+CCR9+α 4 β 7 +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.

Original languageEnglish (US)
Article number8726
JournalNature communications
Volume6
DOIs
StatePublished - Dec 8 2015
Externally publishedYes

ASJC Scopus subject areas

  • General Chemistry
  • General Biochemistry, Genetics and Molecular Biology
  • General
  • General Physics and Astronomy

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