Prime-Boost Immunizations with DNA, Modified Vaccinia Virus Ankara, and Protein-Based Vaccines Elicit Robust HIV-1 Tier 2 Neutralizing Antibodies against the CAP256 Superinfecting Virus

Author:

van Diepen Michiel T.12,Chapman Rosamund12,Douglass Nicola12,Galant Shireen12,Moore Penny L.345ORCID,Margolin Emmanuel126,Ximba Phindile12,Morris Lynn345,Rybicki Edward P.16,Williamson Anna-Lise12

Affiliation:

1. Institute of Infectious Disease and Molecular Medicine, Faculty of Health Science, University of Cape Town, Cape Town, South Africa

2. Division of Medical Virology, Department of Pathology, University of Cape Town, Cape Town, South Africa

3. Centre for HIV and STIs, National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa

4. Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa

5. Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Congella, South Africa

6. Biopharming Research Unit, Department of Molecular and Cell Biology, University of Cape Town, Cape Town, South Africa

Abstract

A vaccine is urgently needed to combat HIV-1, particularly in sub-Saharan Africa, which remains disproportionately affected by the AIDS pandemic and accounts for the majority of new infections and AIDS-related deaths. In this study, two different vaccination regimens were compared. Rabbits that received two DNA primes followed by two modified vaccinia virus Ankara (MVA) and two protein inoculations developed better immune responses than those that received two MVA and three protein inoculations. In addition, DNA and MVA vaccines that expressed mosaic Gag VLPs presenting a stabilized Env antigen elicited better responses than Env alone, which supports the inclusion of Gag VLPs in an HIV-1 vaccine.

Funder

South African Medical Research Council

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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