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      Immune reconstitution in HIV-1 infected patients treated for two years with highly active antiretroviral therapy

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          Abstract

          The aim of this paper was to evaluate the immune reconstitution of HIV-1 patients subjected to highly active antiretroviral therapy (HAART) for two years or more according to CD45RA and CD45RO cell count; determination of IL-2, IFN-gamma, IL-4, IL-10 and TNF-alpha serum levels; CD4+ T and CD8+ T lymphocyte count; and plasma viral load (VL) determination. For this purpose, a cross sectional study was carried out in the Tropical Diseases Area, Botucatu School of Medicine, São Paulo State University, UNESP, Botucatu, São Paulo, Brazil. Between June 2001 and April 2002, 37 HIV-1 infected patients were evaluated, 13 with treatment indication but untreated (G1), 9 subjected to HAART for 5-7 months (G2), and 15 treated for two years or more (G3); both treated groups used medication regularly and without failure. Forty-nine normal individuals were studied as controls (GC-1 and GC-2). There was a tendency (p<0.10) for the predominance of two nucleoside reverse transcriptase inhibitors (NRTI) associated with one non-nucleoside reverse transcriptase inhibitor (NNRTI) regimen in G2; and two NRTI associated with a protease inhibitor (PI) in G3. Statistical differences between groups were seen for CD45RA (G1<[G3=GC-2]; p<0.05) and CD45RO (G1<GC-2<G3; p<0.01) cells, and CD4+ T lymphocyte count (G1<G3; G2-intermediate; p<0.05), VL determination (G1>[G2=G3]; p<0.001), TNF-alpha serum determination ([G1>G3; G2=intermediate]>GC-1; p<0.001), IL-2 (G1<[G2=G3=GC-1]; p<0.01), IFN-gamma ([G1=GC-1]<[GC-2=G3]; p<0.001), IL-4 and IL-10 ([G1=G2=G3]>GC-1; p<0.001), serum cytokine profiles, with a higher proportion of subtype 2 in G1 and mature subtype 0 in G2 and G3 (p<0.005). There was no statistical difference for CD8+ T lymphocyte counts (G1=G2=G3; p<0.50). Consistency was seen between positive correlations of profile 1 definer cytokines (IL-2 and IFN-gamma), CD45RA and CD45RO cells, and CD4+ T lymphocyte counts and between positive correlations of profile 2 definer cytokines (IL-4 and IL-10) with TNF-alpha, and VL. The negative correlations were also consistent as they expressed the inverse of the positives. The variables with the highest number of correlations were IL-2, IFN-gamma, and VL, followed by CD45RA and CD45RO cells, and IL-10. The variables with the lowest number of correlations were CD4+ T and CD8+ T lymphocytes. The results express the partial but important immune reconstitution in HIV-1 infected individuals with the interference of HAART and the importance of cytokines especially IL-2 and IFN-gamma, and CD45RA and CD45RO cells as surrogate markers of this reconstitution.

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          Biostatistical Analysis

          Presents a broad collection of data analysis techniques suitable for biological investigations, either as an introductory textbook assuming no prior knowledge of statistics, or as a reference on concepts and procedures of statistical analysis for professional use in the biological disciplines. Each
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            TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties.

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              Type 1/Type 2 immunity in infectious diseases.

              T helper type 1 (Th1) lymphocytes secrete secrete interleukin (IL)-2, interferon-gamma, and lymphotoxin-alpha and stimulate type 1 immunity, which is characterized by intense phagocytic activity. Conversely, Th2 cells secrete IL-4, IL-5, IL-9, IL-10, and IL-13 and stimulate type 2 immunity, which is characterized by high antibody titers. Type 1 and type 2 immunity are not strictly synonymous with cell-mediated and humoral immunity, because Th1 cells also stimulate moderate levels of antibody production, whereas Th2 cells actively suppress phagocytosis. For most infections, save those caused by large eukaryotic pathogens, type 1 immunity is protective, whereas type 2 responses assist with the resolution of cell-mediated inflammation. Severe systemic stress, immunosuppression, or overwhelming microbial inoculation causes the immune system to mount a type 2 response to an infection normally controlled by type 1 immunity. In such cases, administration of antimicrobial chemotherapy and exogenous cytokines restores systemic balance, which allows successful immune responses to clear the infection.
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                Author and article information

                Journal
                jvatitd
                Journal of Venomous Animals and Toxins including Tropical Diseases
                J. Venom. Anim. Toxins incl. Trop. Dis
                Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) (Botucatu, SP, Brazil )
                1678-9199
                2006
                : 12
                : 1
                : 91-109
                Affiliations
                [02] Botucatu São Paulo orgnameSão Paulo State University orgdiv1Botucatu School of Medicine orgdiv2Applied Immunology Laboratory of Tropical Diseases Brazil
                [03] Botucatu São Paulo orgnameBotucatu Hemocenter Brazil
                [04] Botucatu São Paulo orgnameSão Paulo State University orgdiv1Botucatu School of Veterinary Medicine and Animal Husbandry Brazil
                [01] Botucatu São Paulo orgnameSão Paulo State University orgdiv1Botucatu School of Medicine orgdiv2Department of Tropical Diseases and Imaging Diagnosis Brazil
                Article
                S1678-91992006000100008 S1678-9199(06)01200108
                10.1590/S1678-91992006000100008
                6073c937-6a3a-49f8-8088-bfbe4df1c024

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 26 September 2005
                : 28 March 2005
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 30, Pages: 19
                Product

                SciELO Brazil

                Categories
                Original Papers

                immune reconstitution,antiretroviral,HAART,cytokines,CD45RA,CD45RO,HIV

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