<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Bissa M</submitter><pubmed_abstract>Simian or Human immunodeficiency virus (SIV or HIV) vaccines based on V1-deleted envelope virus-like particles, delivered by the DNA/ALVAC platforms, followed by the ΔV1gp120 boost formulated in Alum, protect 50% and 80% of macaques from mucosal infection with SIV&lt;sub>mac251&lt;/sub> or Simian-Human immunodeficiency virus, respectively. Adding the Army Liposome Formulation + QS21 (ALFQ) adjuvant to the ΔV1gp120+Alum boost (ALFQA) may enhance protective immune responses. Here, we show that ALFQA protects 58% of female macaques from infection following eleven exposures to SIV&lt;sub>mac251&lt;/sub>, achieving 79% vaccine efficacy. The ALFQA vaccine regimen augments mucosal CD73&lt;sup>+&lt;/sup>CD163&lt;sup>+&lt;/sup> M2-like macrophages and NKp44&lt;sup>+&lt;/sup> innate lymphoid cells (ILCs), while reducing NKG2A&lt;su</pubmed_abstract><journal>Nature communications</journal><pagination>8571</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12480912</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>HIV vaccine candidate ΔV1gp120 formulated in ALFQA adjuvant augments mucosal immunity in female macaques.</pubmed_title><pmcid>PMC12480912</pmcid><pubmed_authors>Matyas GR</pubmed_authors><pubmed_authors>Goldfarbmuren KC</pubmed_authors><pubmed_authors>Washington-Parks R</pubmed_authors><pubmed_authors>Gutowska A</pubmed_authors><pubmed_authors>N'guessan KF</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Pise-Masison CA</pubmed_authors><pubmed_authors>Alving R</pubmed_authors><pubmed_authors>Cardozo T</pubmed_authors><pubmed_authors>McKinnon K</pubmed_authors><pubmed_authors>Basu S</pubmed_authors><pubmed_authors>Doster MN</pubmed_authors><pubmed_authors>Montefiori DC</pubmed_authors><pubmed_authors>Rahman MA</pubmed_authors><pubmed_authors>Rao M</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Sarkis S</pubmed_authors><pubmed_authors>Franchini G</pubmed_authors><pubmed_authors>Kanchetty NR</pubmed_authors><pubmed_authors>Silva de Castro I</pubmed_authors><pubmed_authors>Bissa M</pubmed_authors><pubmed_authors>Schifanella L</pubmed_authors><pubmed_authors>Woode EK</pubmed_authors><pubmed_authors>Paquin-Proulx D</pubmed_authors><pubmed_authors>Brown S</pubmed_authors></additional><is_claimable>false</is_claimable><name>HIV vaccine candidate ΔV1gp120 formulated in ALFQA adjuvant augments mucosal immunity in female macaques.</name><description>Simian or Human immunodeficiency virus (SIV or HIV) vaccines based on V1-deleted envelope virus-like particles, delivered by the DNA/ALVAC platforms, followed by the ΔV1gp120 boost formulated in Alum, protect 50% and 80% of macaques from mucosal infection with SIV&lt;sub>mac251&lt;/sub> or Simian-Human immunodeficiency virus, respectively. Adding the Army Liposome Formulation + QS21 (ALFQ) adjuvant to the ΔV1gp120+Alum boost (ALFQA) may enhance protective immune responses. Here, we show that ALFQA protects 58% of female macaques from infection following eleven exposures to SIV&lt;sub>mac251&lt;/sub>, achieving 79% vaccine efficacy. The ALFQA vaccine regimen augments mucosal CD73&lt;sup>+&lt;/sup>CD163&lt;sup>+&lt;/sup> M2-like macrophages and NKp44&lt;sup>+&lt;/sup> innate lymphoid cells (ILCs), while reducing NKG2A&lt;su</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T22:55:27.992Z</modification><creation>2026-05-02T03:11:51.261Z</creation></dates><accession>S-EPMC12480912</accession><cross_references><pubmed>41022728</pubmed><doi>10.1038/s41467-025-63610-z</doi></cross_references></HashMap>