Author
Listed:
- Matthew R. Hepworth
(Perelman School of Medicine, University of Pennsylvania
Institute for Immunology, Perelman School of Medicine, University of Pennsylvania)
- Laurel A. Monticelli
(Institute for Immunology, Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- Thomas C. Fung
(Perelman School of Medicine, University of Pennsylvania
Institute for Immunology, Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- Carly G. K. Ziegler
(ImmunoDynamics Group, Programs in Computational Biology and Immunology, Memorial Sloan-Kettering Cancer Center)
- Stephanie Grunberg
(Perelman School of Medicine, University of Pennsylvania)
- Rohini Sinha
(Perelman School of Medicine, University of Pennsylvania)
- Adriana R. Mantegazza
(Perelman School of Medicine, University of Pennsylvania)
- Hak-Ling Ma
(Inflammation and Immunology Research Unit, Biotherapeutics Research and Development, Pfizer Worldwide R&D, Cambridge, Massachusetts 02140, USA)
- Alison Crawford
(Institute for Immunology, Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- Jill M. Angelosanto
(Institute for Immunology, Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- E. John Wherry
(Institute for Immunology, Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- Pandelakis A. Koni
(Cancer Immunology, Inflammation & Tolerance Program, Georgia Health Sciences University Cancer Center)
- Frederic D. Bushman
(Perelman School of Medicine, University of Pennsylvania)
- Charles O. Elson
(University of Alabama at Birmingham)
- Gérard Eberl
(Lymphoid Tissue Development Unit, Institute Pasteur, 75724 Paris, France
Centre National de la Recherche Scientifique, URA 1961, 75724 Paris, France)
- David Artis
(Institute for Immunology, Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania
School of Veterinary Medicine, University of Pennsylvania)
- Gregory F. Sonnenberg
(Perelman School of Medicine, University of Pennsylvania
Institute for Immunology, Perelman School of Medicine, University of Pennsylvania)
Abstract
Group 3 innate lymphoid cells are shown to process and present antigen and to control CD4+ T-cell responses to intestinal commensal bacteria through an MHC-class-II-dependent mechanism.
Suggested Citation
Matthew R. Hepworth & Laurel A. Monticelli & Thomas C. Fung & Carly G. K. Ziegler & Stephanie Grunberg & Rohini Sinha & Adriana R. Mantegazza & Hak-Ling Ma & Alison Crawford & Jill M. Angelosanto & E., 2013.
"Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria,"
Nature, Nature, vol. 498(7452), pages 113-117, June.
Handle:
RePEc:nat:nature:v:498:y:2013:i:7452:d:10.1038_nature12240
DOI: 10.1038/nature12240
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