GB virus C coinfection and HIV-1 disease progression: The Amsterdam Cohort Study

A.K. van der Bij, N. Kloosterboer, M. Prins, B. Boeser-Nunnink, R.B. Geskus, J.M.A. Lange, R.A. Coutinho, H. Schuitemaker

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Abstract

Background. The effect that GB virus C (GBV-C) coinfection has on human immunodeficiency virus type 1 (HIV-1) disease progression is controversial and therefore was studied in 326 homosexual men from the prospective Amsterdam Cohort Studies who had an accurately estimated date of HIV-1 seroconversion and were followed up for a median period of 8 years. Methods. A first plasma sample, obtained shortly after HIV-1 seroconversion, and a last plasma sample, obtained before 1996, were tested for GBV-C RNA and envelope protein-2 antibodies. The effect that GBV-C has on HIV-1 disease progression was studied by use of time-dependent Cox proportional-hazards models with adjustment for baseline variables and time-updated HIV-1 RNA and CD4(+) cell count. Results. Men who lost GBV-C RNA between collection of the first sample and collection of the last sample had a nearly 3-fold-higher risk of HIV-1 disease progression than did men who had never had GBV-C RNA. This effect became much smaller after adjustment for time-updated CD4(+) cell count. Conclusion. Rather than a positive effect of GBV-C RNA presence, a negative effect of GBV-C RNA loss on HIV-1 disease progression was found, which disappeared after adjustment for time-updated CD4(+) cell count. We therefore hypothesize that GBV-C RNA persistence depends on the presence of a sufficient number of CD4(+) cells- and that the CD4(+) cell decrease associated with HIV-1 disease progression is a cause, not a consequence, of GBVC RNA loss
Original languageEnglish
Pages (from-to)678-685
JournalThe Journal of Infectious Diseases
Volume191
Issue number5
DOIs
Publication statusPublished - 2005

Keywords

  • AMC wi-co

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