Changes in hepatitis C viral response after initiation of highly active antiretroviral therapy and control of HIV viremia in chronically co-infected individuals
被引:12
作者:
Kottilil, S
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Kottilil, S
Jagannatha, S
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Jagannatha, S
Lu, A
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Lu, A
Liu, SY
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Liu, SY
McLaughlin, M
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
McLaughlin, M
Metcalf, JA
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Metcalf, JA
Dewar, R
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Dewar, R
Campbell, C
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Campbell, C
Koratich, C
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Koratich, C
Maldarelli, F
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Maldarelli, F
Masur, H
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Masur, H
Polis, MA
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机构:NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
Polis, MA
机构:
[1] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
[2] NCI, SAIC, Bethesda, MD 20892 USA
[3] NCI, HIV Drug Resistance Program, Bethesda, MD 20892 USA
[4] NIH, Dept Crit Care Med, Bethesda, MD 20892 USA
来源:
HIV CLINICAL TRIALS
|
2004年
/
5卷
/
01期
关键词:
HAART;
HCV;
HIV;
D O I:
10.1310/CVEU-980Q-MPRA-XRG8
中图分类号:
R51 [传染病];
学科分类号:
100401 [流行病与卫生统计学];
摘要:
Background: HIV seropositive individuals co-infected with hepatitis C virus (HCV) have an increased risk for liver cirrhosis. We examined the long-term effect of controlling HIV infection with highly active antiretroviral therapy (HAART) on HCV viremia among co-infected patients. Method: HIV/HCV co-infected patients who initiated HAART and were able to control HIV viremia to <500 copies/mL were evaluated. HIV and HCV viremia were measured at each time point from frozen plasma samples by using bDNA methodology. Liver function tests and CD4+ and CD8+ T cell counts of all patients were obtained at each time point. Results: Seventeen co-infected patients met criteria for study from a cohort of 156 patients. Median time to achieve an HIV viral load (VL) <500 copies/mL after initiation of HAART was 28 weeks (range, 5-225 weeks). Thirteen of 17 patients had increases in HCV VL. Slope analysis of HCV VL vs. HIV VL was -0.14 (p =.0496), demonstrating a 0.14 log increase in HCV VL concomitant with control of HIV viremia. HCV viremia returned toward baseline levels in the 16 patients who maintained HIV suppression for 6 months. None cleared HCV after initiation of HAART during this time. Alkaline phosphatase, ALT, and AST levels were not significantly changed from baseline nor correlated with change in HCV VL (p >.05). Conclusion: Control of HIV viremia may result in an early increase in HCV viremia. In this study, for every 1 log decrease of HIV VL there was a 0.14 log increase of HCV VL. The exact mechanism of this flare seen with control of HIV viremia is unknown. However, HAART alone was not able to eliminate or significantly reduce the HCV viremia in this cohort of co-infected patients.