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J Clin Immunol ; 31(4): 681-9, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21491096

RESUMEN

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.


Asunto(s)
Farmacorresistencia Viral/genética , Epítopos de Linfocito T/inmunología , Infecciones por VIH/genética , Transcriptasa Inversa del VIH/genética , VIH-1/genética , Polimorfismo de Nucleótido Simple , Adulto , Anciano , Fármacos Anti-VIH/inmunología , Células Cultivadas , Ensayo de Immunospot Ligado a Enzimas , Epítopos de Linfocito T/genética , Infecciones por VIH/patología , VIH-1/inmunología , Antígeno HLA-A2/genética , Humanos , Interferón gamma/inmunología , Persona de Mediana Edad , Fenotipo , Linfocitos T Citotóxicos/virología
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