<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Walker-Sperling VEK</submitter><funding>NIAID NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of Allergy and Infectious Diseases</funding><funding>Ragon Institute of MGH, MIT and Harvard</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | NIH Office of the Director</funding><funding>Janssen Research and Development</funding><funding>NIGMS NIH HHS</funding><funding>Gilead Sciences</funding><pagination>3463</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9203527</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>The latent viral reservoir is the critical barrier for developing an HIV-1 cure. Previous studies have shown that therapeutic vaccination or broadly neutralizing antibody (bNAb) administration, together with a Toll-like receptor 7 (TLR7) agonist, enhanced virologic control or delayed viral rebound, respectively, following discontinuation of antiretroviral therapy (ART) in SIV- or SHIV-infected rhesus macaques. Here we show that the combination of active and passive immunization with vesatolimod may lead to higher rates of post-ART virologic control compared to either approach alone. Therapeutic Ad26/MVA vaccination and PGT121 administration together with TLR7 stimulation with vesatolimod resulted in 70% post-ART virologic control in SHIV-SF162P3-infected rhesus macaques. These data suggest the potential of combining active and passive immunization targeting different immunologic mechanisms as an HIV-1 cure strategy.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Therapeutic efficacy of combined active and passive immunization in ART-suppressed, SHIV-infected rhesus macaques.</pubmed_title><pmcid>PMC9203527</pmcid><funding_grant_id>UM1 AI164556</funding_grant_id><funding_grant_id>AI124377, AI126603, AI128751, AI129797, AI164556</funding_grant_id><funding_grant_id>OD024917</funding_grant_id><funding_grant_id>R01 AI084794</funding_grant_id><funding_grant_id>T32 GM007445</funding_grant_id><funding_grant_id>T32 AI007387</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Borducchi EN</pubmed_authors><pubmed_authors>Lewis M</pubmed_authors><pubmed_authors>Pau MG</pubmed_authors><pubmed_authors>Barouch DH</pubmed_authors><pubmed_authors>Fray EJ</pubmed_authors><pubmed_authors>Kumar MR</pubmed_authors><pubmed_authors>Siliciano JD</pubmed_authors><pubmed_authors>Mercado NB</pubmed_authors><pubmed_authors>Murry JP</pubmed_authors><pubmed_authors>Walker-Sperling VEK</pubmed_authors><pubmed_authors>Schuitemaker H</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Wegmann F</pubmed_authors><pubmed_authors>Siliciano RF</pubmed_authors><pubmed_authors>Geleziunas R</pubmed_authors><pubmed_authors>Robb ML</pubmed_authors><pubmed_authors>Nkolola JP</pubmed_authors><pubmed_authors>Michael NL</pubmed_authors><pubmed_authors>Chandrashekar A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Therapeutic efficacy of combined active and passive immunization in ART-suppressed, SHIV-infected rhesus macaques.</name><description>The latent viral reservoir is the critical barrier for developing an HIV-1 cure. Previous studies have shown that therapeutic vaccination or broadly neutralizing antibody (bNAb) administration, together with a Toll-like receptor 7 (TLR7) agonist, enhanced virologic control or delayed viral rebound, respectively, following discontinuation of antiretroviral therapy (ART) in SIV- or SHIV-infected rhesus macaques. Here we show that the combination of active and passive immunization with vesatolimod may lead to higher rates of post-ART virologic control compared to either approach alone. Therapeutic Ad26/MVA vaccination and PGT121 administration together with TLR7 stimulation with vesatolimod resulted in 70% post-ART virologic control in SHIV-SF162P3-infected rhesus macaques. These data suggest the potential of combining active and passive immunization targeting different immunologic mechanisms as an HIV-1 cure strategy.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2024-11-07T13:40:37.114Z</modification><creation>2024-11-07T13:40:37.114Z</creation></dates><accession>S-EPMC9203527</accession><cross_references><pubmed>35710819</pubmed><doi>10.1038/s41467-022-31196-5</doi></cross_references></HashMap>