Viral Immunology · 2004 · 17 citations · 19 references
Life SciencesImmunologyInfectious DiseasesAdaptive ImmunityClinical ImmunologyImmunology Of Infectious DiseasesAntiretroviral TherapyAntiviral ImmunityCell-mediated ImmunityCellular Immunity In InfectionImmune MonitoringImmune ReconstitutionBcl-2 Protein ExpressionCd4 Positive T Cell ResponsesCd4 Positive T CellsHighly Active Antiretroviral TherapyHiv Antiretroviral TherapyImmune Reconstitution After Antiretroviral TherapyLymphocyte ApoptosisViral Load Assessment
Correlates of immune reconstitution after highly active antiretroviral therapy (HAART) are not completely understood, in particular as far as viro-immunological discordant responses are concerned. HIV-positive patients on stable HAART for > or = 1 year were recruited. Viro-immunological responses were categorized according to positive or negative area under the curve (AUC) variations for HIV plasma viral load (pVL) and CD4+ T-cell counts measured at least every 4 months. The following parameters were evaluated: lymphocyte spontaneous apoptosis (LSA), intracellular Bcl-2 expression in both CD4-CD45RA+ and CD4-CD45R0+, IL-7 and IL-15 plasma concentrations, and lymphocyte TRECs levels. Sixty-one patients were enrolled. A significant inverse correlation was found between CD4+ T-cell count and pVL AUC (r = 0.45; p = 0.0003). Patients with pVL response had higher levels of Bcl-2 in CD4-CD45R0+ (mean 65,409 MESF vs. 54,018 MESF; p = 0.089) and higher IL-15 (mean 1.34 pg/mL vs. 1.05 pg/mL; p = 0.069, respectively). Higher LSA and lower TRECs levels were found in viro-immunological non-responder patients with respect to those who had viro-immunological response (mean 24.84% vs. 14.89%; p = 0.01, and mean 17,796 copies/10(6) cells vs. 29,251 copies/10(6) cells; p = 0.68, respectively). Virological suppression may allow Bcl-2 and IL-15 hyperexpression during incomplete immune-reconstitution phase, while more complete immune reconstitution appeared to be marked by both high TRECs and low LSA levels, possibly indicating both central and peripheral CD4+ T-cell repopulations at this stage.
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Christophe Piketty, Laurence Weiss, François Thomas et al. · The Journal of Infectious Diseases · 2001 · 157 citations · Full text
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Howard M. Lederman, Paige L. Williams, Julia Wu et al. · The Journal of Infectious Diseases · 2003 · 92 citations · Full text
Leonid Karawajew, V Ruppert, Christian Wuchter et al. · Blood · 2000 · 84 citations
Life Sciences, Immunology, Oncology +17