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J Clin Immunol ; 31(4): 681-9, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21491096

RESUMO

Many drug-resistance mutations in HIV-1 reverse transcriptase fall within cytotoxic T lymphocytes (CTL) epitopes, but studies of the response to these epitopes in patients with virological failure are lacking. We therefore compared IFN-γ ELISPOT responses to the YV9 epitope (RT181-189) covering the lamivudine resistance mutation, M184V, in HLA-A2(+) antiretroviral treatment (ART)-naive patients (n = 19), to those found in HLA-A2(+) patients with virological failure (n = 15). Ten ART-naive patients had an ELISPOT response to the wild-type epitope that cross-reacted with the mutant epitope. Two patients with virological failure showed a specific response to the 184V mutant epitope. Responses against YV9 were strongly associated (p = 0.005) with the presence of a 177E mutation, and the same tendency was observed in an independent cohort of patients (n = 22). These results indicate that variants in flanking residues may influence CTL responses to conserved subdominant HIV-1 epitopes.


Assuntos
Farmacorresistência Viral/genética , Epitopos de Linfócito T/imunologia , Infecções por HIV/genética , Transcriptase Reversa do HIV/genética , HIV-1/genética , Polimorfismo de Nucleotídeo Único , Adulto , Idoso , Fármacos Anti-HIV/imunologia , Células Cultivadas , ELISPOT , Epitopos de Linfócito T/genética , Infecções por HIV/patologia , HIV-1/imunologia , Antígeno HLA-A2/genética , Humanos , Interferon gama/imunologia , Pessoa de Meia-Idade , Fenótipo , Linfócitos T Citotóxicos/virologia
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