Maternal Humoral Immune Responses Do Not Predict Postnatal HIV-1 Transmission Risk in Antiretroviral-Treated Mothers from the IMPAACT PROMISE Study

Author:

Hompe Eliza D.1,Jacobson Denise L.2,Eudailey Joshua A.3,Butler Kevin2,Edwards Whitney34,Pollara Justin34,Brummel Sean S.2,Fouda Genevieve G.35,Chinula Lameck6,Kamanga Melvin7,Kinikar Aarti8,Moodley Dhayendre9,Owor Maxensia10,Fowler Mary Glenn11,Permar Sallie R.35

Affiliation:

1. Duke University School of Medicine, Durham, North Carolina, USA

2. Center for Biostatistics in AIDS Research, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA

3. Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA

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

5. Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA

6. University of North Carolina Project-Malawi, Lilongwe, Malawi

7. Johns Hopkins University Research Project, Blantyre, Malawi

8. Byramjee Jeejeebhoy Government Medical College, Pune, Maharashtra, India

9. Centre for the AIDS Programme of Research in South Africa and School of Clinical Medicine, College of Health Sciences, University of KwaZulu Natal, Durban, South Africa

10. Johns Hopkins University Research Collaboration, Makerere University, Kampala, Uganda

11. Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

Abstract

Each year, >150,000 infants become newly infected with HIV-1 through MTCT despite ART, with up to 42% of infections occurring during breastfeeding. Several factors contribute to continued pediatric infections, including ART nonadherence, the emergence of drug-resistant HIV strains, acute infection during breastfeeding, and poor access to ART in resource-limited areas. A better understanding of the maternal humoral immune responses that provide protection against postnatal transmission in the setting of ART is critical to guide the design of maternal vaccine strategies to further eliminate postnatal HIV transmission. In this study, we found that in women treated with antiretrovirals during pregnancy, there was a positive correlation between plasma viral load and breast milk and plasma IgA responses; however, conclusions regarding odds of MTCT risk were limited by the small sample size. These findings will inform future studies to investigate maternal immune interventions that can synergize with ART to eliminate MTCT during breastfeeding.

Funder

Doris Duke Charitable Foundation

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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