pubmed-article:12438599 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0220847 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0021311 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0029246 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0019733 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0003316 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0042210 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0449450 | lld:lifeskim |
pubmed-article:12438599 | lifeskim:mentions | umls-concept:C0205296 | lld:lifeskim |
pubmed-article:12438599 | pubmed:dateCreated | 2002-11-19 | lld:pubmed |
pubmed-article:12438599 | pubmed:abstractText | A polyepitopic CD8(+)-T-cell response is thought to be critical for control of hepatitis C virus (HCV) infection. Using transgenic mice, we analyzed the immunogenicity and dominance of most known HLA-A2.1 epitopes presented during infection by using vaccines that carry the potential to enter clinical trials: peptides, DNA, and recombinant adenoviruses. The vaccines capacity to induce specific cytotoxic T lymphocytes and interferon gamma-producing cells revealed that immunogenic epitopes are clustered in specific antigens. For two key antigens, flanking regions were shown to greatly enhance the scope of epitope recognition, whereas a DNA-adenovirus prime-boost vaccination strategy augmented epitope immunogenicity, even that of subdominant ones. The present study reveals a clustered organization of HCV immunogenic HLA.A2.1 epitopes and strategies to modulate their dominance. | lld:pubmed |
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pubmed-article:12438599 | pubmed:language | eng | lld:pubmed |
pubmed-article:12438599 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:12438599 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:KienyMarie... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:Op De... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:LoneYu ChunYC | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:HimoudiNourre... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:AbrahamJean-D... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:FournillierAn... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:JoubertAuréli... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:FreidaDelphin... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:LemonnierFran... | lld:pubmed |
pubmed-article:12438599 | pubmed:author | pubmed-author:InchauspéGene... | lld:pubmed |
pubmed-article:12438599 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12438599 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12438599 | pubmed:pagination | 12735-46 | lld:pubmed |
pubmed-article:12438599 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:12438599 | pubmed:articleTitle | Comparative vaccine studies in HLA-A2.1-transgenic mice reveal a clustered organization of epitopes presented in hepatitis C virus natural infection. | lld:pubmed |
pubmed-article:12438599 | pubmed:affiliation | Unité Mixte CNRS-BioMérieux, UMR 2142, Ecole Normale Supérieure, 46 Allée d'Italie, 69364 Lyon Cédex 07, France. | lld:pubmed |
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