You are not currently logged in.
Access JSTOR through your library or other institution:
Impact of Antiretroviral Treatment on Gene Expression in Peripheral Blood Mononuclear Cells from SIVmac251-Infected Macaques
Maryanne T. Vahey, Christian F. Ockenhouse, Zhining Wang, Jake Yalley-Ogunro, Jack Greenhouse, Martin E. Nau and Mark G. Lewis
The Journal of Infectious Diseases
Vol. 196, No. 3 (Aug. 1, 2007), pp. 384-393
Published by: Oxford University Press
Stable URL: http://www.jstor.org/stable/30087400
Page Count: 10
You can always find the topics here!Topics: Infections, T lymphocytes, Genes, Gene expression, Apoptosis, Antiretrovirals, Viruses, Simian immunodeficiency virus, Viral load, Down regulation
Were these topics helpful?See somethings inaccurate? Let us know!
Select the topics that are inaccurate.
Preview not available
Background. A survey of gene expression in peripheral blood mononuclear cells from cynomolgus macaques infected with SIVmac251 was conducted to ascertain the impact of viral infection and successful antiretroviral (ARV) intervention on gene transcription at peak seroconversion, viral set point, and after treatment with 9-R 2 phosphonomethoxypropyl adenine and β-2'3' dideoxy-3'-thia-5 fluorocytidine. Methods. Robust multichip average-normalized data sets generated on Affymetrix GeneChips were analyzed using Significance Analysis of Microarrays (SAM), to determine differential gene expression. Unsupervised learning algorithms and gene-ontology tools were used to elucidate hierarchical relationships and to define the function of significantly enriched biological categories of differentially regulated genes. Gene networks associated with immune response and inflammation impacted by ARV treatment were derived by use of Pathway Architect software. Results. Viral infection results in down-regulation of gene expression, which is greatest by the viral set point. Of the 3647 genes down-regulated at the viral set point, 1033 were up-regulated as the result of successful ARV treatment. There is significant overlap in the identity of these genes. Conclusions. Intervention with successful ARV treatment in macaques infected with SIVmac251 results in the partial reversal of the down-regulated gene expression characteristic of early viral infection.
The Journal of Infectious Diseases © 2007 Oxford University Press