Early short-term treatment with neutralizing human monoclonal antibodies halts SHIV infection in infant macaques

AJ Hessell, JP Jaworski, E Epson, K Matsuda… - Nature medicine, 2016 - nature.com
AJ Hessell, JP Jaworski, E Epson, K Matsuda, S Pandey, C Kahl, J Reed, WF Sutton…
Nature medicine, 2016nature.com
Prevention of mother-to-child transmission (MTCT) of HIV remains a major objective where
antenatal care is not readily accessible. We tested HIV-1–specific human neutralizing
monoclonal antibodies (NmAbs) as a post-exposure therapy in an infant macaque model for
intrapartum MTCT. One-month-old rhesus macaques were inoculated orally with the simian-
human immunodeficiency virus SHIVSF162P3. On days 1, 4, 7 and 10 after virus exposure,
we injected animals subcutaneously with NmAbs and quantified systemic distribution of …
Abstract
Prevention of mother-to-child transmission (MTCT) of HIV remains a major objective where antenatal care is not readily accessible. We tested HIV-1–specific human neutralizing monoclonal antibodies (NmAbs) as a post-exposure therapy in an infant macaque model for intrapartum MTCT. One-month-old rhesus macaques were inoculated orally with the simian-human immunodeficiency virus SHIVSF162P3. On days 1, 4, 7 and 10 after virus exposure, we injected animals subcutaneously with NmAbs and quantified systemic distribution of NmAbs in multiple tissues within 24 h after antibody administration. Replicating virus was found in multiple tissues by day 1 in animals that were not treated. All NmAb-treated macaques were free of virus in blood and tissues at 6 months after exposure. We detected no anti-SHIV T cell responses in blood or tissues at necropsy, and no virus emerged after CD8+ T cell depletion. These results suggest that early passive immunotherapy can eliminate early viral foci and thereby prevent the establishment of viral reservoirs.
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