Self-reactive VH4-34–expressing IgG B cells recognize commensal bacteria

Author:

Schickel Jean-Nicolas1ORCID,Glauzy Salomé1,Ng Yen-Shing1,Chamberlain Nicolas1,Massad Christopher1,Isnardi Isabelle1,Katz Nathan1ORCID,Uzel Gulbu2,Holland Steven M.23,Picard Capucine45,Puel Anne45ORCID,Casanova Jean-Laurent46578ORCID,Meffre Eric1ORCID

Affiliation:

1. Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06510

2. Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892

3. Clinical Genomics Program, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892

4. Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker Hospital for Sick Children, 75015 Paris, France

5. Paris Descartes University, Imagine Institute, 75015 Paris, France

6. Pediatric Hematology-Immunology Unit, Necker Hospital for Sick Children, 75015 Paris, France

7. St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065

8. Howard Hughes Medical Institute, New York, NY 10065

Abstract

The germline immunoglobulin (Ig) variable heavy chain 4–34 (VH4-34) gene segment encodes in humans intrinsically self-reactive antibodies that recognize I/i carbohydrates expressed by erythrocytes with a specific motif in their framework region 1 (FWR1). VH4-34–expressing clones are common in the naive B cell repertoire but are rarely found in IgG memory B cells from healthy individuals. In contrast, CD27+IgG+ B cells from patients genetically deficient for IRAK4 or MYD88, which mediate the function of Toll-like receptors (TLRs) except TLR3, contained VH4-34–expressing clones and showed decreased somatic hypermutation frequencies. In addition, VH4-34–encoded IgGs from IRAK4- and MYD88-deficient patients often displayed an unmutated FWR1 motif, revealing that these antibodies still recognize I/i antigens, whereas their healthy donor counterparts harbored FWR1 mutations abolishing self-reactivity. However, this paradoxical self-reactivity correlated with these VH4-34–encoded IgG clones binding commensal bacteria antigens. Hence, B cells expressing germline-encoded self-reactive VH4-34 antibodies may represent an innate-like B cell population specialized in the containment of commensal bacteria when gut barriers are breached.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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