A dysbiotic microbiome triggers T H 17 cells to mediate oral mucosal immunopathology in mice and humans

Author:

Dutzan Nicolas12ORCID,Kajikawa Tetsuhiro3ORCID,Abusleme Loreto12ORCID,Greenwell-Wild Teresa1,Zuazo Carlos E.1,Ikeuchi Tomoko1ORCID,Brenchley Laurie1,Abe Toshiharu3ORCID,Hurabielle Charlotte45,Martin Daniel6ORCID,Morell Robert J.6,Freeman Alexandra F.7,Lazarevic Vanja8,Trinchieri Giorgio9,Diaz Patricia I.10ORCID,Holland Steven M.7ORCID,Belkaid Yasmine4ORCID,Hajishengallis George3ORCID,Moutsopoulos Niki M.1ORCID

Affiliation:

1. Oral Immunity and Inflammation Unit, NIDCR, NIH, Bethesda, MD 20892, USA.

2. Faculty of Dentistry, University of Chile, 8380492 Santiago, Chile.

3. Department of Microbiology, Penn Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

4. Mucosal Immunology Section, Laboratory of Parasitic Diseases, NIAID, NIH, MD 20892, USA.

5. Inserm U976, Hôpital Saint Louis, Université Paris Diderot, Paris 75010, France.

6. Genomics and Computational Biology Core, NIDCD, NIH, Bethesda, MD 20892, USA.

7. Laboratory of Clinical Immunology and Microbiology (LCIM), NIAID, NIH, Bethesda, MD 20892, USA.

8. Experimental Immunology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.

9. Cancer and Inflammation Program, CCR, NCI, NIH, Bethesda, MD 20892, USA.

10. School of Dental Medicine, UConn Health, Farmington, CT 06030, USA.

Abstract

Combined patient and animal model studies implicate microbiota-triggered T H 17 cells as disease drivers and therapeutic targets in periodontitis.

Funder

Fondation pour la Recherche Médicale

NIAID

NIDCR

NCI Intramural

La Roche-Posay

CEDEF

Philippe Foundation

fondation groupe pasteur mutualité

Société Française de Dermatologie

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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