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Restricted Microbiota and Absence of Cognate TCR Antigen Leads to an Unbalanced Generation of Th17 Cells.

Abstract : Retinoic acid-related orphan receptor (ROR)γt(+) TCRαβ(+) cells expressing IL-17, termed Th17 cells, are most abundant in the intestinal lamina propria. Symbiotic microbiota are required for the generation of Th17 cells, but the requirement for microbiota-derived Ag is not documented. In this study, we show that normal numbers of Th17 cells develop in the intestine of mice that express a single TCR in the absence of cognate Ag, whereas the microbiota remains essential for their development. However, such mice, or mice monocolonized with the Th17-inducing segmented filamentous bacteria, fail to induce normal numbers of Foxp3(+) RORγt(+) T cells, the regulatory counterpart of IL-17(+)RORγt(+) T cells. These results demonstrate that a complex microbiota and cognate Ag are required to generate a properly regulated set of RORγt(+) T cells and Th17 cells.
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https://hal-pasteur.archives-ouvertes.fr/pasteur-00564664
Contributor : Marie-Christine Vougny <>
Submitted on : Wednesday, February 9, 2011 - 3:55:39 PM
Last modification on : Friday, May 29, 2020 - 9:51:04 AM

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Matthias Lochner, Marion Bérard, Shinichiro Sawa, Siona Hauer, Valérie Gaboriau-Routhiau, et al.. Restricted Microbiota and Absence of Cognate TCR Antigen Leads to an Unbalanced Generation of Th17 Cells.. Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2011, 186 (3), pp.1531-7. ⟨10.4049/jimmunol.1001723⟩. ⟨pasteur-00564664⟩

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