Natural polyreactive IgA antibodies coat the intestinal microbiota

Author:

Bunker Jeffrey J.12ORCID,Erickson Steven A.12,Flynn Theodore M.3ORCID,Henry Carole14,Koval Jason C.3,Meisel Marlies14,Jabri Bana14ORCID,Antonopoulos Dionysios A.345ORCID,Wilson Patrick C.14ORCID,Bendelac Albert12ORCID

Affiliation:

1. Committee on Immunology, University of Chicago, Chicago, IL 60637, USA.

2. Department of Pathology, University of Chicago, Chicago, IL 60637, USA.

3. Biosciences Division, Argonne National Laboratory, Argonne, IL 60439, USA.

4. Department of Medicine, University of Chicago, Chicago, IL 60637, USA.

5. Institute for Genomics and Systems Biology, University of Chicago, Chicago, IL 60637, USA.

Abstract

Programmed recognition of microbiota Increasingly, we recognize that the gut is a specialized organ for maintaining microbial symbioses alongside nutritional functions. The gut produces large quantities of immunoglobulin A (IgA), which adheres to the surface of gut microbes. Bunker et al. discovered that antibodies produced by naïve small intestinal plasma cells are recirculated and enriched within Peyer's patches, independently of exogenous antigen and T cell help. The resulting polyreactive IgAs are released into the gut lumen and bind to microbial surface glycans, thus innately recognizing the gut microbiota. Polyreactive IgAs appear to be a product of the coevolution of host and microbiota to maintain symbiotic homeostasis. Science , this issue p. eaan6619

Funder

National Heart, Lung, and Blood Institute

National Institute of General Medical Sciences

National Institute of Allergy and Infectious Diseases

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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