<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Freel SA</submitter><funding>Intramural NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>PHS HHS</funding><pagination>4998-5006</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2863846</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>84(10)</volume><pubmed_abstract>Control of HIV-1 replication following nonsterilizing HIV-1 vaccination could be achieved by vaccine-elicited CD8(+) T-cell-mediated antiviral activity. To date, neither the functional nor the phenotypic profiles of CD8(+) T cells capable of this activity are clearly understood; consequently, little is known regarding the ability of vaccine strategies to elicit them. We used multiparameter flow cytometry and viable cell sorts from phenotypically defined CD8(+) T-cell subsets in combination with a highly standardized virus inhibition assay to evaluate CD8(+) T-cell-mediated inhibition of viral replication. Here we show that vaccination against HIV-1 Env and Gag-Pol by DNA priming followed by recombinant adenovirus type 5 (rAd5) boosting elicited CD8(+) T-cell-mediated antiviral activity aga</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>Phenotypic and functional profile of HIV-inhibitory CD8 T cells elicited by natural infection and heterologous prime/boost vaccination.</pubmed_title><pmcid>PMC2863846</pmcid><funding_grant_id>U01 AI067854</funding_grant_id><funding_grant_id>P30 AI027767</funding_grant_id><funding_grant_id>Z99 AI999999</funding_grant_id><funding_grant_id>AI067854-05</funding_grant_id><funding_grant_id>R01A5779</funding_grant_id><funding_grant_id>U19 AI067854</funding_grant_id><funding_grant_id>P30 AI064518</funding_grant_id><funding_grant_id>P30 AI27767</funding_grant_id><funding_grant_id>P30 AI 64518</funding_grant_id><pubmed_authors>Zarkowsky D</pubmed_authors><pubmed_authors>Cunningham CK</pubmed_authors><pubmed_authors>Chattopadhyay PK</pubmed_authors><pubmed_authors>Roederer M</pubmed_authors><pubmed_authors>Ferrari G</pubmed_authors><pubmed_authors>Lamoreaux L</pubmed_authors><pubmed_authors>Saunders K</pubmed_authors><pubmed_authors>Ochsenbauer C</pubmed_authors><pubmed_authors>Graham BS</pubmed_authors><pubmed_authors>Kappes JC</pubmed_authors><pubmed_authors>Koup RA</pubmed_authors><pubmed_authors>Edmonds TG</pubmed_authors><pubmed_authors>Overman RG</pubmed_authors><pubmed_authors>Haynes BF</pubmed_authors><pubmed_authors>Weinhold KJ</pubmed_authors><pubmed_authors>Freel SA</pubmed_authors><pubmed_authors>Denny TN</pubmed_authors><pubmed_authors>Tomaras GD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phenotypic and functional profile of HIV-inhibitory CD8 T cells elicited by natural infection and heterologous prime/boost vaccination.</name><description>Control of HIV-1 replication following nonsterilizing HIV-1 vaccination could be achieved by vaccine-elicited CD8(+) T-cell-mediated antiviral activity. To date, neither the functional nor the phenotypic profiles of CD8(+) T cells capable of this activity are clearly understood; consequently, little is known regarding the ability of vaccine strategies to elicit them. We used multiparameter flow cytometry and viable cell sorts from phenotypically defined CD8(+) T-cell subsets in combination with a highly standardized virus inhibition assay to evaluate CD8(+) T-cell-mediated inhibition of viral replication. Here we show that vaccination against HIV-1 Env and Gag-Pol by DNA priming followed by recombinant adenovirus type 5 (rAd5) boosting elicited CD8(+) T-cell-mediated antiviral activity aga</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 May</publication><modification>2025-04-04T11:56:02.057Z</modification><creation>2019-03-27T00:30:33Z</creation></dates><accession>S-EPMC2863846</accession><cross_references><pubmed>20200250</pubmed><doi>10.1128/JVI.00138-10</doi><doi>10.1128/jvi.00138-10</doi></cross_references></HashMap>