Journal article
Combination Adenovirus and Protein Vaccines Prevent Infection or Reduce Viral Burden after Heterologous Clade C Simian-Human Immunodeficiency Virus Mucosal Challenge
Journal of virology, Vol.92(2), e01092-17
01/15/2018
DOI: 10.1128/JVI.01092-17
PMCID: PMC5752948
PMID: 29093095
Abstract
HIV vaccine development is focused on designing immunogens and delivery methods that elicit protective immunity. We evaluated a combination of adenovirus (Ad) vectors expressing HIV 1086.C (clade C) envelope glycoprotein (Env), SIV Gag p55, and human pegivirus GBV-C E2 glycoprotein. We compared replicating simian (SAd7) with nonreplicating human (Ad4) adenovirus-vectored vaccines paired with recombinant proteins in a novel prime-boost regimen in rhesus macaques, with the goal of eliciting protective immunity against SHIV challenge. In both vaccine groups, plasma and buccal Env-specific IgG, tier 1 heterologous neutralizing antibodies, and antibody-dependent cell-mediated viral inhibition were readily generated. High Env-specific T cell responses elicited in all vaccinees were significantly greater than responses targeting Gag. After three intrarectal exposures to heterologous tier 1 clade C SHIV, all 10 sham-vaccinated controls were infected, whereas 4/10 SAd7- and 3/10 Ad4-vaccinated macaques remained uninfected or maintained tightly controlled plasma viremia. Time to infection was significantly delayed in SAd7-vaccinated macaques compared to the controls. Cell-associated and plasma virus levels were significantly lower in each group of vaccinated macaques compared to controls; the lowest plasma viral burden was found in animals vaccinated with the SAd7 vectors, suggesting superior immunity conferred by the replicating simian vectors. Furthermore, higher V1V2-specific binding antibody titers correlated with viral control in the SAd7 vaccine group. Thus, recombinant Ad plus protein vaccines generated humoral and cellular immunity that was effective in either protecting from SHIV acquisition or significantly reducing viremia in animals that became infected, consequently supporting additional development of replicating Ad vectors as HIV vaccines.
There is a well-acknowledged need for an effective AIDS vaccine that protects against HIV infection and limits
viral replication and associated pathogenesis. Although replicating virus vectors have been advanced as HIV vaccine platforms, there have not been any direct comparisons of the replicating to the nonreplicating format. The present study directly compared the replicating SAd7 to nonreplicating Ad4 vectors in macaques and demonstrated that in the SAd7 vaccine group, the time to infection was significantly delayed compared to the control group, and V1V2 Env-specific binding antibodies correlated with viral outcomes. Viral control was significantly enhanced in vaccinated macaques compared to controls, and in infected SAd7-vaccinated macaques compared to Ad4-vaccinated macaques, suggesting that this vector may have conferred more effective immunity. Because blocking infection is so difficult with current vaccines, development of a vaccine that can limit viremia if infection occurs would be valuable. These data support further development of replicating adenovirus vectors.
Details
- Title: Subtitle
- Combination Adenovirus and Protein Vaccines Prevent Infection or Reduce Viral Burden after Heterologous Clade C Simian-Human Immunodeficiency Virus Mucosal Challenge
- Creators
- Delphine C Malherbe - Oregon National Primate Research CenterJason Mendy - PAX Scientific (United States)Lo Vang - PAX Scientific (United States)Philip T Barnette - Oregon National Primate Research CenterJason Reed - Oregon National Primate Research CenterSamir K Lakhashe - Texas Biomedical Research InstituteJoshua Owuor - Texas Biomedical Research InstituteJohannes S Gach - University of California, IrvineAlfred W Legasse - Oregon National Primate Research CenterMichael K Axthelm - Oregon National Primate Research CenterCelia C LaBranche - Duke UniversityDavid Montefiori - Duke UniversityDonald N Forthal - University of California, IrvineByung Park - Oregon National Primate Research CenterJames M Wilson - University of PennsylvaniaJames H McLinden - Veterans Health AdministrationJinhua Xiang - Veterans Health AdministrationJack T Stapleton - Veterans Health AdministrationJonah B Sacha - Oregon National Primate Research CenterBarton F Haynes - Duke UniversityHua-Xin Liao - Duke UniversityRuth M Ruprecht - Texas Biomedical Research InstituteJonathan Smith - PAX Scientific (United States)Marc Gurwith - PAX Scientific (United States)Nancy L Haigwood - Oregon National Primate Research CenterJeff Alexander - PAX Scientific (United States)
- Resource Type
- Journal article
- Publication Details
- Journal of virology, Vol.92(2), e01092-17
- DOI
- 10.1128/JVI.01092-17
- PMID
- 29093095
- PMCID
- PMC5752948
- NLM abbreviation
- J Virol
- ISSN
- 0022-538X
- eISSN
- 1098-5514
- Grant note
- R01 AI100703 / NIAID NIH HHS R01 AI118581 / NIAID NIH HHS I01 BX000207 / BLRD VA R44 AI091546 / NIAID NIH HHS P51 OD011092 / NIH HHS P51 OD011133 / NIH HHS
- Language
- English
- Date published
- 01/15/2018
- Academic Unit
- Microbiology and Immunology; Infectious Diseases; Internal Medicine
- Record Identifier
- 9984297316202771
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