Clade C HIV-1 Envelope Vaccination Regimens Differ in Their Ability To Elicit Antibodies with Moderate Neutralization Breadth against Genetically Diverse Tier 2 HIV-1 Envelope Variants

Author:

Burton Samantha12,Spicer Lori M.12,Charles Tysheena P.12,Gangadhara Sailaja12,Reddy Pradeep B. J.12,Styles Tiffany M.12,Velu Vijayakumar12,Kasturi Sudhir Pai12,Legere Traci2,Hunter Eric312,Pulendran Bali312,Amara Rama124,Hraber Peter5ORCID,Derdeyn Cynthia A.312

Affiliation:

1. Emory Vaccine Center, Emory University, Atlanta, Georgia, USA

2. Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA

3. Department of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia, USA

4. Department of Microbiology and Immunology, Emory University, Atlanta, Georgia, USA

5. Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, New Mexico, USA

Abstract

Despite much progress, we still do not have a clear understanding of how to elicit a protective neutralizing antibody response against HIV-1 through vaccination. There have been great strides in the development of envelope immunogens that mimic the virus particle, but less is known about how different vaccination modalities and adjuvants contribute to shaping the antibody response. We compared seven different vaccines that were administered to rhesus macaques and that delivered the same envelope protein through various modalities and with different adjuvants. The results demonstrate that some vaccine components are better than others at eliciting neutralizing antibodies with breadth.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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