Serum neopterin, an immune activation marker, independently predicts disease progression in advanced HIV-1 infection

Background. CD4(+) T lymphocyte ( CD4) counts and plasma human immunodeficiency virus ( HIV) type 1 RNA concentrations predict clinical outcome in HIV-1 infection. Our objective was to assess the independent prognostic value for disease progression of soluble markers of immune system activation. Methods. This retrospective marker- validation study utilized previously obtained clinical and laboratory data, including CD4(+) cell counts, and made use of stored frozen serum samples to assay for levels of beta(2)- microglobulin, neopterin, endogenous interferon, triglycerides, interleukin- 6, soluble tumor necrosis factor-alpha receptor II, and HIV-1 RNA, and to determine HIV genotypic reverse- transcriptase inhibitor resistance. The 152 patients who participated in this study represented a subsample of participants in AIDS Clinical Trials Group ( ACTG) 116B/ 117, a randomized trial that demonstrated the clinical benefit of didanosine over zidovudine monotherapy in persons with advanced HIV-1 infection. Marker data were analyzed in relation to protocol-defined clinical disease progression, using Cox proportional hazards models. Results. The median duration of follow-up was 344 days. Elevated baseline values for neopterin (P =.0009), endogenous interferon (P =.00039) and interleukin-6 (P =.0007) were each associated with greater subsequent risk of clinical disease progression. In a head-to-head comparison that was adjusted for CD4(+) cell count (P= .0165) and HIV-1 RNA level (P =.1220), we found that elevated values for neopterin (P = .0002) and, to a lesser extent, endogenous inferon (P= .0053) were the strongest predictors of increased risk of clinical disease progression 6 months later. Conclusions. Soluble markers of immune activation add prognostic information to CD4 counts and viral load for risk of disease progression in advanced HIV-1 infection. The robust performance of neopterin, an in-expensive and reliably measured serum marker, supports its potential suitability for patient monitoring, particularly in resource-limited settings.