Author
Listed:
- Rafael M. Rezende
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Andre P. da Cunha
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Chantal Kuhn
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Stephen Rubino
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Hanane M’Hamdi
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School
Rheumatology Unit, Karolinska Institute)
- Galina Gabriely
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Tyler Vandeventer
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Shirong Liu
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Ron Cialic
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
- Natalia Pinheiro-Rosa
(Institute of Biological Sciences, Federal University of Minas Gerais)
- Rafael P. Oliveira
(Institute of Biological Sciences, Federal University of Minas Gerais)
- Jellert T. Gaublomme
(Harvard University
Harvard University)
- Nikolaus Obholzer
(Program in Translational NeuroPsychiatric Genomics, Institute for the Neurosciences, Brigham and Women’s Hospital)
- James Kozubek
(Program in Translational NeuroPsychiatric Genomics, Institute for the Neurosciences, Brigham and Women’s Hospital)
- Nathalie Pochet
(Program in Translational NeuroPsychiatric Genomics, Institute for the Neurosciences, Brigham and Women’s Hospital
Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard)
- Ana M. C. Faria
(Institute of Biological Sciences, Federal University of Minas Gerais)
- Howard L. Weiner
(Ann Romney Center for Neurologic Diseases, Brigham and Women’s Hospital, Harvard Medical School)
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.
Suggested Citation
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 & J, 2015.
"Identification and characterization of latency-associated peptide-expressing γδ T cells,"
Nature Communications, Nature, vol. 6(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms9726
DOI: 10.1038/ncomms9726
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