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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

GB virus type C infection modulates T-cell activation independently of HIV-1 viral load

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Autor(es):
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Maidana-Giret, Maria Teresa [1] ; Silva, Tania M. [1] ; Sauer, Mariana M. [1] ; Tomiyama, Helena [1] ; Levi, Jose Eduardo [2] ; Bassichetto, Katia C. [3] ; Nishiya, Anna [4] ; Diaz, Ricardo S. [1] ; Sabino, Ester C. [4] ; Palacios, Ricardo [1] ; Kallas, Esper Georges [1, 5]
Número total de Autores: 11
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Div Infect Dis, Sao Paulo - Brazil
[2] Univ Sao Paulo, Inst Trop Med, BR-01246903 Sao Paulo - Brazil
[3] Publ Hlth Dept Sao Paulo, Sao Paulo - Brazil
[4] Fundacao Prosangue, Hemoctr, Sao Paulo - Brazil
[5] Univ Sao Paulo, Lab Invest Med 60, Div Clin Immunol & Allergy, BR-01246903 Sao Paulo - Brazil
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: AIDS; v. 23, n. 17, p. 2277-2287, NOV 13 2009.
Citações Web of Science: 35
Resumo

Background: Many clinical studies have suggested a beneficial effect of GB virus type C (GBV-C) on the course of HIV-1 infection, but the mechanisms involved in such amelioration are not clear. As recent evidence has implicated cellular activation in HIV-1 pathogenesis, we investigated the effect of GBV-C viremia on T-cell activation in early HIV-1 infection. Methods: Forty-eight recently infected HIV-1 patients (23 GBV-C viremic) were evaluated for T-cell counts, expanded immunophenotyping GBV-C RNA detection, and HIV-1 viral load. Nonparametric univariate and multivariate analyses were carried out to identify variables associated with cellular activation, including GBV-C status, HIV-1 viral load, T lymphocyte counts, and CD38 and chemokine (C-C motif) receptor 5 (CCR5) surface expression. Finding: We not only confirmed the positive correlation between HIV-1 viral load and the percentage of T cells positive for CD38(+)CD8(+) but also observed that GBV-C viremic patients had a lower percentage of T cells positive for CD38(+)CD4(+), CD38(+)CD8(+), CCR5(+)CD4(+), and CCR5(+)CD8(+) compared with HIV-1-infected patients who were not GBV-C viremic. In regression models, GBV-C RNA(+) status was associated with a reduction in the CD38 on CD4(+) or CD8(+) T cells and CCR5(+) on CD8(+) T cells, independent of the HIV-1 viral load or CD4(+) and CD8(+) T-cell counts. These results were also supported by the lower expression of CD69 and CD25 in GBV-C viremic patients. Interpretation: The association between GBV-C replication and lower T-cell activation may be a key mechanism involved in the protection conferred by this virus against HIV-1 disease progression to immunodeficiency in HIV-1-infected patients. (C) 2009 Wolters Kluwer Health | Lippincott Williams \& Wilkins (AU)

Processo FAPESP: 04/15856-9 - Análise prospectiva das características virológicas e imunológicas em indivíduos com infecção recente pelo HIV-1 das cidades de São Paulo e Santos, SP
Beneficiário:Ricardo Sobhie Diaz
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 05/01072-9 - A influência da infecção pelo GB virus com virus da hepatite G (HGV) na evolução da doença pelo HIV em mulheres
Beneficiário:José Eduardo Levi
Modalidade de apoio: Auxílio à Pesquisa - Regular