Distribution of the Human Immunodeficiency Virus Coreceptors CXCR4 and CCR5 on Leukocytes of Persons with Human Immunodeficiency Virus Type 1 Infection and Pulmonary Tuberculosis: Implications for Pathogenesis
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作者:
Sharon Shalekoff
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机构:University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
Sharon Shalekoff
Stella Pendle
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机构:University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
Stella Pendle
Dave Johnson
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机构:University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
Dave Johnson
Desmond J. Martin
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机构:University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
Desmond J. Martin
Caroline T. Tiemessen
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机构:University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
Caroline T. Tiemessen
机构:
[1] University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
[2] Sizwe Tropical Diseases Hospital,Department of Virology
[3] University of the Witwatersrand,AIDS Virus Research Unit, National Institute for Virology, and Department of Virology
Expression of CXCR4 was significantly reduced from normal on all cell subsets of persons with pulmonary tuberculosis (TB group), with HIV-1 infection (HIV group), and those with both infections (HIV/TB group), except for on monocytes in the HIV group. The reductions were most notable in the two TB groups. Interestingly, the duration of antituberculosis treatment was significantly negatively correlated with the expression of CXCR4 on CD4+ and CD8+CD45RO+ cells, monocytes and NK cells, viral load, and proportions of CD38-expressing CD8+ lymphocytes, in HIV/TB patients. By contrast, CCR5 expression on most cell subsets analyzed was increased in all the disease groups, except for on monocytes in the two TB groups. There was no change in CCR5 expression on CD4+ cells when based on the disease groupings. However, higher proportions of CD4+CD45RA+ and CD8+ lymphocytes as well as B cells expressing CCR5 correlated with advancing HIV-1 disease, as did decreased proportions of CXCR4-expressing CD4+CD45RA+ cells.