© 1999 by Oxford University Press
Brief report. Surrogate markers of disease progression in HIV-infected children in Rio de Janeiro, Brazil
A Laboratorio de Imunologia Clinica, Departamento de Imunologia, IOC-FIOCRUZ, Rio de Janeiro, Brazil B Instituto de Pediatria e Puercultura Martagao Gesteira, Universidade Federal do Rio de Janeiro, Brazil C Ambulatorio do Banco da Providencia, Rio de Janeiro, Brazil D Departamento de Estatistica, IME, Universidade do Estado do Rio de Janeiro, Brazil Z Corresponding author Tel: +55 21 280 1486 Fax: +55 21 280 1589 E-mail: ortigao@gene.dbbm.fiocruz.br
In order to test the predictive value of immune complex-dissociated p24 antigenaemia (ICD-p24Ag), ß2 microglobulin (ß2-M), and neopterin as markers of disease progression, 53 HIV-1 infected children (mean age 68 months) and nine HIV-negative controls (mean age 65 months) were studied prospectively for 9 months. Five were classified in category E (CDC-1994) and seroreverted during the study, 14 in category A, nine in category B, and 25 in category C (CDC-1994). Blood samples were taken at medium intervals of 61 days and tested for ICD-p24Ag, ß2 microglobulin, and neopterin. The results were correlated with clinical outcome and CD4-lymphocyte counts. All three groups (A,B,C) of symptomatic children had similar positivity in an ICD-p24Ag test (48.1, 58.8, and 51.0 per cent, respectively), and all in group E had negative p24 antigenaemia. ß2 microglobulin and neopterin tests showed no correlation with clinical stages of HIV-1 infection. There was no significant correlation between these three tests with age-matched CD4 lymphocyte counts (p>0.05). In contrast, the CD4 lymphocyte count correlated well with disease stages. These data suggest that the markers evaluated in the present study do not correlate well with clinical findings or with CD4 lymphocyte counts. Of all the markers tested, CD4 count was the best to predict prognosis of HIV disease in this cohort.