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The objective of this study was to monitor the changes in the immune system of HIV-infected children with moderate or severe immunodeficiency after highly active antiretroviral therapy (HAART), comprising a follow-up study in 14 HIV-infected children on HAART at two time points separated approximately by 11·8 ± 0·4 (9·9; 15·4) months. HIV-infected children had significantly lower TREC levels than the control group, but 1 year after HAART the levels increased significantly ( P < 0·05). In contrast, viral load (VL) did not change significantly. A positive correlation between T cell receptor excision circle (TREC) levels and both CD4+ T cell absolute counts ( r = 0·558; P = 0·05) and percentages ( r = 0·625; P = 0·030) was found. During follow-up on HAART, the percentages and absolute counts of naive CD4+ and CD8+ T cell subsets were increased significantly ( P < 0·05). CD4+ CD45RAhi+ CD62L+, CD4+ CD45RA+ and CD4+ CD38+ percentages, and the CD8+ CD45RAhi+ CD62L+ counts reached similar values to the control group. Also, CD8+ CD45RO+ CD38+ and CD8+ CD45RO+ percentages, and CD8+ CD45RO+ CD38+ absolute counts ( P < 0·05) decreased with respect to the baseline. Lymphoproliferative responses to pokeweed mitogen (PWM) before HAART were lower in HIV-infected children than the control group, but they recovered to normal levels after a year on HAART. Tumour necrosis factor (TNF)- α and interferon (IFN)- γ production by PHA-activated peripheral blood mononuclear cells (PBMC) was lower before HAART ( P < 0·001), but reached similar levels to the control group 1 year after HAART. In HIV-infected children IgG, IgG1 and IgG3 plasma levels decreased significantly after HAART. The immune system reconstitution induced by HAART in HIV-infected children seems to be the consequence of decreased immune system activation and naive T cell reconstitution, mainly of thymic origin. [ABSTRACT FROM AUTHOR]

The objective of this study was to investigate the relationship between peripheral blood CD4[sup +] T cell subsets and routine viro-immunological markers in vertically HIV-1-infected children undergoing highly active antiretroviral therapy (HAART). CD4[sup +] and CD8[sup +] T cell subsets were examined by three-colour flow cytometry. Plasma viraemia was quantified by a standardized molecular assay. A negative correlation between the %CD4[sup +] T cells and both viral load and the %CD8[sup +] T cells was observed. A strong positive correlation between the %CD4 T cells and naïve, CD38[sup +] and non-activated CD4[sup +] T cell subsets was found, whereas the %CD4 T cells correlated negatively with the numbers of memory, activated and memory-activated CD4[sup +] T cell subsets. Elevated percentages of CD8 T cells were associated with increased memory and CD4[sup +] CD62L-T cell subsets, whereas the naïve and CD4[sup +] HLA-DR[sup ]CD38[sup +] subsets negatively correlated with the CD8%. Co-expression of CD62L on memory CD4[sup +] cells and high expression of HLA-DR (but not of CD38) were associated with high viral load. No association between viral load and naïve CD4[sup +] T cells was observed. Specific CD4[sup +] T cell subsets may be more informative than routine surrogate markers in defining the evolution of HIV infection and immune reconstitution in children. [ABSTRACT FROM AUTHOR]