Your browser doesn't support javascript.
loading
The Contribution of Extracellular Nef to HIV-Induced Pathogenesis.
Olivetta, Eleonora; Arenaccio, Claudia; Manfredi, Francesco; Anticoli, Simona; Federico, Maurizio.
Afiliação
  • Olivetta E; National AIDS Center, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161 Rome, Italy. eleonora.olivetta@iss.it.
Curr Drug Targets ; 17(1): 46-53, 2016.
Article em En | MEDLINE | ID: mdl-26424397
ABSTRACT
Nef is an accessory protein expressed exclusively in primate lentiviruses. It is devoid of enzymatic activities while interacting with several cell proteins as an adaptor/scaffold protein. Intracellular functions of Nef largely account for many pathogenic effects observed in AIDS disease. Nef, despite lacking known secretory pathways, can be detected in plasma of HIV-1-infected patients at the concentration varing from 5 to 10 ng/ml. Remarkably, the levels of Nef in plasma of HIV patients do not correlate with viral load or number of CD4(+) T lymphocytes, and persist during antiretroviral therapy. Here, we review literature data describing how Nef can be transmitted from HIV-1- infected cells to bystander ones, and the effects of extracellular Nef in different cell types. Overall, large part of experimental evidences supports the idea that extracellular Nef plays a relevant role in AIDS pathogenesis. Hence, efforts focused on the identification of Nef-inhibiting drugs would be of relevance to establish new therapeutic approaches supporting current antiretroviral therapies.
Assuntos
Buscar no Google
Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Comunicação Parácrina / Produtos do Gene nef do Vírus da Imunodeficiência Humana Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Comunicação Parácrina / Produtos do Gene nef do Vírus da Imunodeficiência Humana Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article