<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(7)</volume><submitter>Sriwanthana B</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The design of a globally effective vaccine rests on the identification of epitopes capable of eliciting effective cytotoxic T lymphocyte (CTL) responses across multiple HIV clades in different populations. This study aims to discern the effect of HLA polymorphisms and the cross-clade reactivity or clade-specificity of epitopes in Thailand where HIV-1 CRF01_AE is circulating.&lt;h4>Materials and methods&lt;/h4>14 peptides based on consensus HIV-1 CRF01_AE amino acid sequences were designed for use in IFN-γ ELISpot assays and (51)Cr release assays among 66 HIV-1 CRF01_AE-infected Thai patients. For ELISpot responders carrying HLA alleles currently unknown to restrict CRF01_AE epitopes, in silico epitope-HLA prediction was performed.&lt;h4>Results&lt;/h4>29/66 (43.9%) patients recognized at least one peptide. In total 79 responses were seen against all 14 peptides. 28/79 (35.4%) of the responses were in patients with HLA alleles previously reported to restrict CRF01_AE epitopes, 24/79 (30.4%) responses were in individuals with HLA alleles previously reported to restrict epitopes of HIV clades other than CRF01_AE, and the remaining 27/79 (34.2%) responses were not associated with HLA alleles previously known to restrict HIV epitopes. In silico epitope prediction detected 19 novel, epitope-HLA combinations, and 11/19 (57.9%) were associated with HLA-C alleles. We further confirmed a novel HLA restriction of a previously identified HIV-1 Gag epitope [p24(122-130): PPIPVGDIY (PY9)] by HLA-B*40:01 with a standard (51)Cr release assay.&lt;h4>Discussion&lt;/h4>CTL recognition sites in HIV-1 Gag were similar among different clades but the HLA restriction differed in Thai patients. This disparity in HLA restriction along different populations illustrated the importance of clade- and population-specific HLA analysis prior to CTL vaccine design.</pubmed_abstract><journal>PloS one</journal><pagination>e41696</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3407236</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The effect of HLA polymorphisms on the recognition of Gag epitopes in HIV-1 CRF01_AE infection.</pubmed_title><pmcid>PMC3407236</pmcid><pubmed_authors>Mori M</pubmed_authors><pubmed_authors>Sriwanthana B</pubmed_authors><pubmed_authors>Nishimura S</pubmed_authors><pubmed_authors>Pathipvanich P</pubmed_authors><pubmed_authors>Ariyoshi K</pubmed_authors><pubmed_authors>Sawanpanyalert P</pubmed_authors><pubmed_authors>Tanaka M</pubmed_authors><pubmed_authors>Miura T</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of HLA polymorphisms on the recognition of Gag epitopes in HIV-1 CRF01_AE infection.</name><description>&lt;h4>Introduction&lt;/h4>The design of a globally effective vaccine rests on the identification of epitopes capable of eliciting effective cytotoxic T lymphocyte (CTL) responses across multiple HIV clades in different populations. This study aims to discern the effect of HLA polymorphisms and the cross-clade reactivity or clade-specificity of epitopes in Thailand where HIV-1 CRF01_AE is circulating.&lt;h4>Materials and methods&lt;/h4>14 peptides based on consensus HIV-1 CRF01_AE amino acid sequences were designed for use in IFN-γ ELISpot assays and (51)Cr release assays among 66 HIV-1 CRF01_AE-infected Thai patients. For ELISpot responders carrying HLA alleles currently unknown to restrict CRF01_AE epitopes, in silico epitope-HLA prediction was performed.&lt;h4>Results&lt;/h4>29/66 (43.9%) patients recognized at least one peptide. In total 79 responses were seen against all 14 peptides. 28/79 (35.4%) of the responses were in patients with HLA alleles previously reported to restrict CRF01_AE epitopes, 24/79 (30.4%) responses were in individuals with HLA alleles previously reported to restrict epitopes of HIV clades other than CRF01_AE, and the remaining 27/79 (34.2%) responses were not associated with HLA alleles previously known to restrict HIV epitopes. In silico epitope prediction detected 19 novel, epitope-HLA combinations, and 11/19 (57.9%) were associated with HLA-C alleles. We further confirmed a novel HLA restriction of a previously identified HIV-1 Gag epitope [p24(122-130): PPIPVGDIY (PY9)] by HLA-B*40:01 with a standard (51)Cr release assay.&lt;h4>Discussion&lt;/h4>CTL recognition sites in HIV-1 Gag were similar among different clades but the HLA restriction differed in Thai patients. This disparity in HLA restriction along different populations illustrated the importance of clade- and population-specific HLA analysis prior to CTL vaccine design.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2025-07-03T03:04:45.563Z</modification><creation>2025-07-03T03:04:45.563Z</creation></dates><accession>S-EPMC3407236</accession><cross_references><pubmed>22848569</pubmed><doi>10.1371/journal.pone.0041696</doi></cross_references></HashMap>