Literature DB >> 11114829

Comparison of T-cell subsets' reconstitution after 12 months of highly active antiretroviral therapy initiated during early versus advanced states of HIV disease.

C Tortajada1, F Garcia, M Plana, T Gallart, M J Maleno, J M Miró, J M Gatell.   

Abstract

UNLABELLED: This research comprised a pilot open prospective clinical study comparing T-cell subset reconstitution in antiretroviral-naive patients, after 12 months of HAART when treatment was initiated in early stages (ES; n = 18) of infection versus advanced stages (AS; n = 20). CONTROL GROUP: 10 healthy HIV-negative individuals. Immunophenotypic markers were evaluated before and after 6-and 12-months' therapy. Functional assays were performed in one subset.
RESULTS: Viral load (VL) was < 200 copies/ml in all patients. Median percentages of CD4+ pretherapy were 33% and 6%, respectively, in the ES and AS groups, increment after 12 months of therapy was +15% and +13% respectively. Only the ES group achieved normal values. Declines of CD8+ percentage were significantly higher in the ES (-18%) than in the AS group (-2%). CD4+ memory and naive cells in the ES group were similar to those of controls before treatment and did not change after therapy. In contrast, CD4+ memory and naive cells in the AS group did not reach normal levels despite treatment. In the ES group, there was a significant increment in CD8+ naive cells (+8%) and a decrement in CD8+CD38+ cells (-17%), both populations reached values close to normal, whereas these subsets remained far from normal in the AS group. Improvement of lymphoproliferative response after therapy was observed in both groups. One patient in the ES group showed positive LPR against p24 after treatment. After 12 months' highly active antiretroviral therapy, only those who began such therapy in ES disease reached values within the range of healthy controls. To achieve a more complete immunologic reconstitution, early initiation of potent antiretroviral therapy should be recommended.

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Year:  2000        PMID: 11114829     DOI: 10.1097/00042560-200012010-00002

Source DB:  PubMed          Journal:  J Acquir Immune Defic Syndr        ISSN: 1525-4135            Impact factor:   3.731


  8 in total

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3.  Memory responses in human immunodeficiency virus type 1-infected individuals with long-term viral load suppression are independent of CD4 cell nadir.

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4.  Lower CD4+ T lymphocyte nadirs may indicate limited immune reconstitution in HIV-1 infected individuals on potent antiretroviral therapy: analysis of immunophenotypic marker results of AACTG 5067.

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Journal:  J Clin Immunol       Date:  2005-03       Impact factor: 8.317

Review 5.  CD4(+) T-cell depletion in HIV infection: mechanisms of immunological failure.

Authors:  Afam A Okoye; Louis J Picker
Journal:  Immunol Rev       Date:  2013-07       Impact factor: 12.988

6.  Antigen-presenting cell modulation induces a memory response to p24 in peripheral blood leukocytes from human immunodeficiency virus-infected individuals.

Authors:  Michael A Kolber; Maria O Saenz
Journal:  Clin Diagn Lab Immunol       Date:  2003-09

7.  Impact of HIV on CD8+ T cell CD57 expression is distinct from that of CMV and aging.

Authors:  Sulggi A Lee; Elizabeth Sinclair; Hiroyu Hatano; Priscilla Y Hsue; Lorrie Epling; Frederick M Hecht; David R Bangsberg; Jeffrey N Martin; Joseph M McCune; Steven G Deeks; Peter W Hunt
Journal:  PLoS One       Date:  2014-02-27       Impact factor: 3.240

8.  The effect of interrupted anti-retroviral treatment on the reconstitution of memory and naive T cells during tuberculosis treatment in HIV patients with active pulmonary tuberculosis.

Authors:  Sophie Nalukwago; Christina L Lancioni; Joy Baseke Oketcho; Dave H E Canaday; W Henry Boom; Lonzy Ojok; Harriet Mayanja-Kizza
Journal:  Afr Health Sci       Date:  2017-12       Impact factor: 0.927

  8 in total

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