<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang H</submitter><funding>Medical Research Council</funding><pagination>993-1002</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4444423</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(9)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>The HLA-A30-B13-C06 haplotype is reported to be associated with slow disease progression in the HIV-1-infected Northern Han Chinese population, but the mechanism remains unknown.&lt;h4>Design&lt;/h4>Gag-specific T-cell responses and gag sequencing were performed in nine B' clade HIV-1-infected HLA-A30-B13-C06-positive slow progressors to understand HLA-associated viral control.&lt;h4>Methods&lt;/h4>Interferon-γ ELISPOT assays were performed to determine the Gag-specific T-cell responses and cross-reactivity to variant peptides. Longitudinal HIV-1 gag sequencing was performed at the clonal level.&lt;h4>Results&lt;/h4>The overlapping peptides (OLP)-48: RQANFLGKIWPSHKGRPGNF (RL42 Gag434-453); OLP-2: GQLDRWEKIRLRPGGKKKYR (RL42 Gag11-30); OLP-15: VQNLQGQMVHQPISPRTLNA (RL42 Gag135-154) and OLP-1</pubmed_abstract><journal>AIDS (London, England)</journal><pubmed_title>Multilayered HIV-1 gag-specific T-cell responses contribute to slow progression in HLA-A*30-B*13-C*06-positive patients.</pubmed_title><pmcid>PMC4444423</pmcid><funding_grant_id>G1001046</funding_grant_id><funding_grant_id>MR/L018942/1</funding_grant_id><funding_grant_id>G0600520</funding_grant_id><pubmed_authors>Dong T</pubmed_authors><pubmed_authors>Zhao B</pubmed_authors><pubmed_authors>An M</pubmed_authors><pubmed_authors>Jiang F</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Han X</pubmed_authors><pubmed_authors>Shang H</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Xu J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multilayered HIV-1 gag-specific T-cell responses contribute to slow progression in HLA-A*30-B*13-C*06-positive patients.</name><description>&lt;h4>Objective&lt;/h4>The HLA-A30-B13-C06 haplotype is reported to be associated with slow disease progression in the HIV-1-infected Northern Han Chinese population, but the mechanism remains unknown.&lt;h4>Design&lt;/h4>Gag-specific T-cell responses and gag sequencing were performed in nine B' clade HIV-1-infected HLA-A30-B13-C06-positive slow progressors to understand HLA-associated viral control.&lt;h4>Methods&lt;/h4>Interferon-γ ELISPOT assays were performed to determine the Gag-specific T-cell responses and cross-reactivity to variant peptides. Longitudinal HIV-1 gag sequencing was performed at the clonal level.&lt;h4>Results&lt;/h4>The overlapping peptides (OLP)-48: RQANFLGKIWPSHKGRPGNF (RL42 Gag434-453); OLP-2: GQLDRWEKIRLRPGGKKKYR (RL42 Gag11-30); OLP-15: VQNLQGQMVHQPISPRTLNA (RL42 Gag135-154) and OLP-1</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2026-05-02T01:28:02.926Z</modification><creation>2026-04-07T17:30:31.175Z</creation></dates><accession>S-EPMC4444423</accession><cross_references><pubmed>25756195</pubmed><doi>10.1097/QAD.0000000000000652</doi></cross_references></HashMap>