Decreased HIV-associated T cell apoptosis by HIV protease inhibitors

Antiretroviral treatment of patients infected with HIV results in improvements in CD4+ T cell number. Emerging evidence suggests that some of the improvements in CD4+ T cell number that occur in response to protease inhibitor (PI) therapy may not be accounted for solely by enhanced viral suppression...

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Veröffentlicht in:AIDS research and human retroviruses 2000-04, Vol.16 (6), p.559-567
Hauptverfasser: PHENIX, B. N, ANGEL, J. B, BADLEY, A. D, MANDY, F, KRAVCIK, S, PARATO, K, CHAMBERS, K. A, GALLICANO, K, HAWLEY-FOSS, N, CASSOL, S, CAMERON, D. W
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Sprache:eng
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Zusammenfassung:Antiretroviral treatment of patients infected with HIV results in improvements in CD4+ T cell number. Emerging evidence suggests that some of the improvements in CD4+ T cell number that occur in response to protease inhibitor (PI) therapy may not be accounted for solely by enhanced viral suppression, implying that PI may directly affect T cell survival. Since HIV T cell depletion is associated with enhanced apoptosis, we analyzed the effect of PIs on T cell apoptosis. In vitro treatment of peripheral blood lymphocytes (PBLs) from HIV-infected but untreated patients with reverse transcriptase inhibitors (RTIs) does not alter apoptosis, whereas PI treatment rapidly reduces CD4+ and CD8+ T cell apoptosis. In contrast, PI treatment does not alter apoptosis in PBL blasts from HIV-negative patients, or in Jurkat T cells. Consistent with this observation, 8 days of PI therapy in HIV-infected patients does not significantly alter plasma viremia, yet results in significant inhibition of CD4+ and CD8+ T cell apoptosis. The inhibitory effects of PI on apoptosis have implications concerning the treatment of HIV and its pathogenesis.
ISSN:0889-2229
1931-8405
DOI:10.1089/088922200308972