Intranasal priming induces local lung-resident B cell populations that secrete protective mucosal antiviral IgA

Author:

Oh Ji Eun12ORCID,Song Eric1ORCID,Moriyama Miyu1ORCID,Wong Patrick1ORCID,Zhang Sophia1,Jiang Ruoyi1ORCID,Strohmeier Shirin3,Kleinstein Steven H.145ORCID,Krammer Florian3ORCID,Iwasaki Akiko167ORCID

Affiliation:

1. Department of Immunobiology, Yale School of Medicine, New Haven, CT 06519, USA.

2. Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.

3. Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

4. Department of Pathology, Yale School of Medicine, New Haven, CT 06520, USA.

5. Interdepartmental Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06520, USA.

6. Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven CT 06520, USA.

7. Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.

Abstract

A heterogeneous population of cells secreting mucosal IgA confers protection against influenza virus infection.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine,Immunology

Reference36 articles.

1. Exploiting Mucosal Immunity for Antiviral Vaccines

2. The establishment of resident memory B cells in the lung requires local antigen encounter

3. Multi-Faceted Functions of Secretory IgA at Mucosal Surfaces

4. IgA Function in Relation to the Intestinal Microbiota

5. Epithelial transcytosis of monomeric IgA and IgG cross-linked through antigen to polymeric IgA. A role for monomeric antibodies in the mucosal immune system;Kaetzel C. S.;J. Immunol.,1994

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