ORIGINAL RESEARCH article
Front. Microbiol.
Sec. Infectious Agents and Disease
Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1592647
This article is part of the Research TopicResearch Advances and Challenges in Emerging and Re-Emerging Viral DiseasesView all 19 articles
Combining a rhesus cytomegalovirus/SIV vaccine with neutralizing antibody to protect against SIV challenge in rhesus macaques
Provisionally accepted- 1Immunology & Microbial Science, The Scripps Research Institute, La Jolla, CA, United States
- 2Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, United States
- 3National Institutes of Health (NIH), Bethesda, Maryland, United States
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A vaccine is widely regarded as necessary for the control of the HIV pandemic and eventual eradication of AIDS. Neutralizing antibodies and MHC-E-restricted CD8+ T cells have both been shown capable of vaccine protection against the simian counterpart of HIV, SIV, in rhesus macaques. Here we provide preliminary evidence that combining these orthogonal antiviral mechanisms can provide increased protection against SIV challenge such that replication arrest observed following vaccination with a rhesus cytomegalovirus (RhCMV/SIV)-based vaccine was enhanced in the presence of passively administered incompletely protective levels of neutralizing antibody. The report invites studies involving larger cohorts of macaques and alternate routes of providing neutralizing antibody.
Keywords: HIV, SIV, neutralizing antibodies, T cells, Vaccine, non-human primate (macaque)
Received: 14 Mar 2025; Accepted: 08 May 2025.
Copyright: © 2025 Coppola, Parren, Bastidas, Saye, Malvin, Jardine, Gilbride, Ojha, Feltham, Morrow, Barber-Axthelm, Bochart, Fast, Oswald, Shoemaker, Lifson, Picker, Burton and Hansen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Louis J Picker, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, 97006-3448, Oregon, United States
Dennis R Burton, Immunology & Microbial Science, The Scripps Research Institute, La Jolla, 92037, CA, United States
Scott G Hansen, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, 97006-3448, Oregon, United States
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