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HIV does not replicate in naive CD4 T cells stimulated with CD3/CD28.
Roederer, M; Raju, P A; Mitra, D K; Herzenberg, L A; Herzenberg, L A.
Afiliación
  • Roederer M; Department of Genetics, Stanford University, California 94305-5125, USA. roederer@darwin.stanford.edu
J Clin Invest ; 99(7): 1555-64, 1997 Apr 01.
Article en En | MEDLINE | ID: mdl-9119999
ABSTRACT
In this report, we demonstrate that the T cell tropic strain of HIV, LAI, does not replicate in naive CD4 T cells stimulated by cross-linking CD3 and CD28. In contrast, LAI replicates well in memory CD4 T cells stimulated in the same way. Unlike this physiologically relevant stimulation, PHA stimulates productive LAI replication in both naive and memory T cells. These studies were conducted with highly purified (FACS-isolated) subsets of CD4 T cells identified by expression of both CD45RA and CD62L. Remixing of purified T cells showed that naive T cells do not suppress LAI replication in memory T cells and that memory T cells do not restore LAI expression in naive T cells. The suppression of productive LAI replication in naive T cells is not due to differential expression of viral coreceptors, nor is it due to inhibition of activation of the important HIV transcription factors, nuclear factor-kappaB and activator protein-1. The inherent resistance of naive T cells to productive HIV infection, coupled with their proliferative advantage as demonstrated here, provides a sound basis for proposed clinical therapies using ex vivo expansion and reinfusion of CD4 T cells from HIV-infected adults.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Replicación Viral / Linfocitos T CD4-Positivos / VIH / Complejo CD3 / Antígenos CD28 Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Clin Invest Año: 1997 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Replicación Viral / Linfocitos T CD4-Positivos / VIH / Complejo CD3 / Antígenos CD28 Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Clin Invest Año: 1997 Tipo del documento: Article País de afiliación: Estados Unidos