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Research Article Free access | 10.1172/JCI119605

Dynamics of HIV-1 mRNA expression in patients with long-term nonprogressive HIV-1 infection.

M Comar, C Simonelli, S Zanussi, P Paoli, E Vaccher, U Tirelli, and M Giacca

Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

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Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

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Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

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Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

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Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

Find articles by Vaccher, E. in: JCI | PubMed | Google Scholar

Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

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Molecular Medicine Unit, International Centre for Genetic Engineering and Biotechnology, 34100 Trieste, Italy.

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Published August 15, 1997 - More info

Published in Volume 100, Issue 4 on August 15, 1997
J Clin Invest. 1997;100(4):893–903. https://doi.org/10.1172/JCI119605.
© 1997 The American Society for Clinical Investigation
Published August 15, 1997 - Version history
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Abstract

A large number of evidences indicate that progression of HIV disease is driven by an increase in viral burden. It is still unclear, however, to what extent this is contributed by the dysregulation of the molecular mechanisms governing virus gene expression at the transcriptional or posttranscriptional levels. To address this issue, several quantitative virologic parameters (including provirus transcriptional activity and splicing pattern) were analyzed in individuals with nonprogressive HIV infection and compared with those of a matched group of progressor patients. Exact quantification was achieved by a competitive PCR procedure using a multicompetitor template. Nonprogressors were characterized by striking differences in the levels of viremia, provirus copy number, and overall levels of all viral mRNA classes in peripheral blood mononuclear cells. Additionally, the transcriptional activity of the proviral DNA in these patients was mainly engaged in the production of multiprocessed transcripts, with a pattern resembling the early phases of the experimental infection. Taken together, these results show that both viral load and provirus transcription pattern are remarkably different in infected individuals nonprogressing toward overt disease, and further support the notion that disease progression is accompanied by a change in the kinetics of HIV gene expression.

Version history
  • Version 1 (August 15, 1997): No description

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