Akkermansia muciniphila induces intestinal adaptive immune responses during homeostasis

Author:

Ansaldo Eduard1ORCID,Slayden Leianna C.1ORCID,Ching Krystal L.1ORCID,Koch Meghan A.1ORCID,Wolf Natalie K.1,Plichta Damian R.2ORCID,Brown Eric M.2ORCID,Graham Daniel B.2345,Xavier Ramnik J.2345ORCID,Moon James J.6ORCID,Barton Gregory M.1ORCID

Affiliation:

1. Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA.

2. Broad Institute of MIT and Harvard, Cambridge, MA, USA.

3. Center for Computational and Integrative Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

4. Department of Molecular Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

5. Center for Microbiome Informatics and Therapeutics, MIT, Cambridge, MA, USA.

6. Center for Immunology and Inflammatory Diseases and Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Abstract

Context shapes anticommensal immunity The gut bacterium Akkermansia muciniphila is associated with protection from obesity, enhanced wound healing, and augmented antitumor responses. Ansaldo et al. found that this microbe induces antigen-specific immunoglobulin G1 (IgG1) antibodies generated by B cells with CD4 + T cell help. This is in contrast to most anticommensal responses, which involve the T cell–independent production of IgA antibodies. In a gnotobiotic setting in which all components of the microbiome are defined, A. muciniphila –specific T cells expanded only when A. muciniphila was present. The T cells primarily displayed a phenotype associated with B cell help. However, in mice with a conventional gut microbiota, other proinflammatory A. muciniphila –specific T cell populations also expanded. Thus, anti– A. muciniphila immunity is context dependent, which may explain the variable immune responses to this microbe reported in patients. Science , this issue p. 1179

Funder

National Institute of Allergy and Infectious Diseases

National Institute of Diabetes and Digestive and Kidney Diseases

Burroughs Wellcome Fund

Crohn's and Colitis Foundation of America

Fundación Bancaria Caixa d’Estalvis i Pensions de Barcelona

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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