Your browser doesn't support javascript.
loading
Viral inhibition assay: a CD8 T cell neutralization assay for use in clinical trials of HIV-1 vaccine candidates.
J Infect Dis ; 201(5): 720-9, 2010 Mar.
Article em En | MEDLINE | ID: mdl-20132004
ABSTRACT
We have characterized an assay measuring CD8 T cell-mediated inhibition of human immunodeficiency virus (HIV) type 1 replication, demonstrating specificity and reproducibility and employing a panel of primary HIV-1 isolates. The assay uses relatively simple autologous cell culture and enzyme-linked immunosorbent assay, avoids generation of T cell clones, and can be performed with <2 million peripheral blood mononuclear cells. Efficient CD8 T cell-mediated cross-clade inhibition of HIV-1 replication in vitro was demonstrated in antiretroviral therapy-naive HIV-1-infected subjects with controlled viral replication in vivo but not in viremic subjects. An HIV-1 vaccine candidate, consisting of DNA and recombinant adenovirus 5 vectors tested in a phase I clinical trial, induced CD8 T cells that efficiently inhibited HIV-1 in a HLA-I-dependent manner. Assessment of direct antiviral T cell function by this assay provides additional information to guide vaccine design and the prioritizing of candidates for further clinical trials.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes de Neutralização / HIV-1 / Vacinas contra a AIDS / Linfócitos T CD8-Positivos Tipo de estudo: Clinical_trials / Diagnostic_studies / Evaluation_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Infect Dis Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes de Neutralização / HIV-1 / Vacinas contra a AIDS / Linfócitos T CD8-Positivos Tipo de estudo: Clinical_trials / Diagnostic_studies / Evaluation_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Infect Dis Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Reino Unido