Rare Detection of Antiviral Functions of Polyclonal IgA Isolated from Plasma and Breast Milk Compartments in Women Chronically Infected with HIV-1

Author:

Tay Matthew Zirui12,Kunz Erika L.1,Deal Aaron1,Zhang Lu1,Seaton Kelly E.1,Rountree Wes1,Eudailey Joshua A.1,Heptinstall Jack1,McRaven Michael D.3,Matias Edgar3,McGuire Erin1,Yates Nicole L.1,Perez Lautaro G.14,Montefiori David C.14,Overman R. Glenn1,Hope Thomas J.3ORCID,Shen Xiaoying1ORCID,Kalilani Linda5,Fouda Genevieve G.16,Tomaras Georgia D.1247ORCID,Permar Sallie R.126

Affiliation:

1. Duke Human Vaccine Institute, Duke University, Durham, North Carolina, USA

2. Department of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina, USA

3. Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA

4. Department of Surgery, Duke University, Durham, North Carolina, USA

5. College of Medicine, University of Malawi, Blantyre, Malawi

6. Department of Pediatrics, Duke University, Durham, North Carolina, USA

7. Department of Immunology, Duke University, Durham, North Carolina, USA

Abstract

Antibodies within the mucosa are part of the first line of defense against mucosal pathogens. Evaluating mucosal antibody isotypes, specificities, and antiviral functions in relationship to the systemic antibody profile can provide insights into whether the antibody response is coordinated in response to mucosal pathogens. In a natural immunity cohort of HIV-infected lactating women, we mapped the fine specificity and function of IgA in breast milk and plasma and compared these with the autologous IgG responses. Antigen specificities and functions differed between IgG and IgA, with antiviral functions (neutralization and phagocytosis) predominantly mediated by the IgG fraction in both milk and plasma. Furthermore, the specificity of milk IgA differed from that of systemic IgA. Our data suggest that milk IgA and systemic IgA should be separately examined as potential correlates of risk. Preventive vaccines may need to employ different strategies to elicit functional antiviral immunity by both antibody isotypes in the mucosa.

Funder

HHS | National Institutes of Health

Bill and Melinda Gates Foundation

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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