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pubmed-article:9071432pubmed:abstractTextThe temporal relationship between viral and surrogate markers and clinical status was analyzed prospectively every 8 weeks in 34 asymptomatic HIV-1-infected persons. After 3 years, 25 persons remained clinically healthy whereas 9 persons showed clinical progression. In accordance with other reports we found that at study entry HIV-RNA load was predictive of clinical progression. All markers tested evolved significantly in time in both progressors and nonprogressors. The HIV RNA load in plasma and HIV DNA load in T cells were linearly related only in nonprogressors. In addition, the RNA/DNA ratio during follow-up was significantly higher in progressors, indicating a higher replication rate in progressors. The HIV DNA load correlated inversely with CD4+ T cell counts and positively with p24 antigenemia in both nonprogressors and progressors. A significant correlation of HIV DNA load with SI phenotype occurred in progressors only. HIV RNA levels correlated with beta 2-microglobulin level and with p24 antigenemia but not with SI phenotype. These three markers can all routinely be measured in plasma; however, only the HIV RNA levels appear to be informative for clinical progression. Six to 8 months before clinical progression, an SI phenotype switch, increased HIV RNA in plasma, and decreased CD4+ T cell counts were all indicative of an impending clinical event.lld:pubmed
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pubmed-article:9071432pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:9071432pubmed:articleTitleProspective longitudinal analysis of viral load and surrogate markers in relation to clinical progression in HIV type 1-infected persons.lld:pubmed
pubmed-article:9071432pubmed:affiliationDepartment of Clinical Viro-Immunology, Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, Amsterdam, The Netherlands.lld:pubmed
pubmed-article:9071432pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9071432pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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