Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14767
ชื่อเรื่อง: ZAP-70 positive cells in treated and untreated HIV-1 infected patients
ผู้แต่ง: Surapanon S.
Sukwit S.
Chuenchitra T.
Santiwattanakul S.
วันที่เผยแพร่: 2010
บทคัดย่อ: ZAP-70 is a critical protein tyrosine kinase in T-cell activation and proliferation processes. Defective recruitment of ZAP-70 molecules results in termination of the T-cell receptor (TCR) signal transduction pathway. Impairment of this pathway is one of the early markers of disease progression in HIV-1 infected individuals. T-cell dysfunction in HIV infected patients may be connected to a defect in the proximal TCR signaling cascade. To evaluate this presumption, the numbers and mean fluorescence intensity (MFI) of ZAP-70 positive cells in patients with treated and untreated HIV-1 infection and healthy controls were analyzed by flow cytometry. A correlation between the MFI in ZAP 70 molecules and the viral load was evaluated. A total of 41 HIV-1 infected patients, 30 patients on HAART and 11 untreated patients, and 11 healthy controls were enrolled. The data show ZAP-70+/CD4+ cells in treated and untreated HIV-1 infected individuals had a greater MFI of ZAP-70 molecules than those from healthy controls (p<0.001). The inverse correlation between the percentage of CD4+cells and the MFI of ZAP-70+/CD4+ T-cells was significant (r = -0.5; p <0.01). A stronger correlation between the percentage of CD4+/CD25+ cells and the MFI of ZAP-70+/CD4+ cells was observed (r = -0.6; p<0.01). However, no significant correlation was seen between the MFI of the ZAP-70+/CD4+cells and the viral load in patients with untreated HIV-1 infection (r = -0.4, p = 0.16). For HIV-1 treated patients, the viral loads were too low to detect so it was not possible to calculate the correlation. Elevated MFI levels of ZAP-70 molecules in CD4+cells in HIV infected patients may be associated with an inability to further activate T-cells.
URI: https://ir.swu.ac.th/jspui/handle/123456789/14767
https://www.scopus.com/inward/record.uri?eid=2-s2.0-76949106657&partnerID=40&md5=1d8bca967f2a69540b2d75abb404dbf9
ISSN: 1251562
Appears in Collections:Scopus 1983-2021

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