<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ramezani-Rad P</submitter><funding>NIAID NIH HHS</funding><funding>NIH</funding><funding>NIH HHS</funding><pagination>e185292</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11996878</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>135(8)</volume><pubmed_abstract>Induction of durable protective immune responses is the main goal of prophylactic vaccines, and adjuvants play a role as drivers of such responses. Despite advances in vaccine strategies, development of a safe and effective HIV vaccine remains a significant challenge. Use of an appropriate adjuvant is crucial to the success of HIV vaccines. Here we assessed the saponin/MPLA nanoparticle (SMNP) adjuvant with an HIV envelope (Env) trimer, evaluating the safety and effect of multiple variables - including adjuvant dose (16-fold dose range), immunization route, and adjuvant composition - on the establishment of Env-specific memory T and B cell (TMem and BMem) responses and long-lived plasma cells in nonhuman primates (NHPs). Robust BMem were detected in all groups, but a 6-fold increase was ob</pubmed_abstract><journal>The Journal of clinical investigation</journal><pubmed_title>The saponin monophosphoryl lipid A nanoparticle adjuvant induces dose-dependent HIV vaccine responses in nonhuman primates.</pubmed_title><pmcid>PMC11996878</pmcid><funding_grant_id>S10OD025052</funding_grant_id><funding_grant_id>UM1AI144462</funding_grant_id><funding_grant_id>S10 OD025052</funding_grant_id><funding_grant_id>UM1 AI144462</funding_grant_id><funding_grant_id>U24 AI126683</funding_grant_id><funding_grant_id>51OD011107</funding_grant_id><funding_grant_id>P51 OD011107</funding_grant_id><pubmed_authors>Marina-Zarate E</pubmed_authors><pubmed_authors>Irvine DJ</pubmed_authors><pubmed_authors>Sagar SL</pubmed_authors><pubmed_authors>Myers A</pubmed_authors><pubmed_authors>Ramezani-Rad P</pubmed_authors><pubmed_authors>Maiorino L</pubmed_authors><pubmed_authors>Sayeed E</pubmed_authors><pubmed_authors>Burton DR</pubmed_authors><pubmed_authors>Crotty S</pubmed_authors><pubmed_authors>Lemnios AA</pubmed_authors><pubmed_authors>Budai M</pubmed_authors><pubmed_authors>Burton I</pubmed_authors><pubmed_authors>Pires IS</pubmed_authors><pubmed_authors>Wagner A</pubmed_authors><pubmed_authors>Schief WR</pubmed_authors><pubmed_authors>Cottrell CA</pubmed_authors><pubmed_authors>Pradhan A</pubmed_authors><pubmed_authors>Kasturi SP</pubmed_authors><pubmed_authors>Groschel B</pubmed_authors><pubmed_authors>Van Rompay KK</pubmed_authors><pubmed_authors>Melo MB</pubmed_authors><pubmed_authors>Lopez PG</pubmed_authors><pubmed_authors>Hangartner L</pubmed_authors><pubmed_authors>Kaczmarek Michaels K</pubmed_authors><pubmed_authors>Kumar D</pubmed_authors><pubmed_authors>Stiegler G</pubmed_authors><pubmed_authors>Pallerla S</pubmed_authors><pubmed_authors>Bloom NI</pubmed_authors></additional><is_claimable>false</is_claimable><name>The saponin monophosphoryl lipid A nanoparticle adjuvant induces dose-dependent HIV vaccine responses in nonhuman primates.</name><description>Induction of durable protective immune responses is the main goal of prophylactic vaccines, and adjuvants play a role as drivers of such responses. Despite advances in vaccine strategies, development of a safe and effective HIV vaccine remains a significant challenge. Use of an appropriate adjuvant is crucial to the success of HIV vaccines. Here we assessed the saponin/MPLA nanoparticle (SMNP) adjuvant with an HIV envelope (Env) trimer, evaluating the safety and effect of multiple variables - including adjuvant dose (16-fold dose range), immunization route, and adjuvant composition - on the establishment of Env-specific memory T and B cell (TMem and BMem) responses and long-lived plasma cells in nonhuman primates (NHPs). Robust BMem were detected in all groups, but a 6-fold increase was ob</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-06-01T14:53:49.946Z</modification><creation>2026-04-08T13:33:56.438Z</creation></dates><accession>S-EPMC11996878</accession><cross_references><pubmed>40036068</pubmed><doi>10.1172/JCI185292</doi></cross_references></HashMap>