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艾滋病毒和丙型肝炎病毒合并感染的管理挑战。

Challenges in the management of HIV and hepatitis C virus co-infection.

作者信息

Lee Winston, Dieterich Douglas

机构信息

Mount Sinai Medical Center, 1 Gustave L. Levy Place, Box 1118, New York, NY 10029, USA.

出版信息

Drugs. 2004;64(7):693-700. doi: 10.2165/00003495-200464070-00002.

DOI:10.2165/00003495-200464070-00002
PMID:15025544
Abstract

Hepatitis C virus (HCV) has become a significant contributor to morbidity and mortality to those infected with HIV since the introduction of highly active antiretroviral therapy (HAART). The presence of HIV clearly has a negative effect on the natural history of HCV, although there is some debate over whether HCV influences the natural history of HIV. Given the prevalence of co-infection and the accelerated liver damage from HCV, treatment of chronic HCV infection is an important consideration in patients co-infected with HIV. There are few studies of pegylated interferon and ribavirin in co-infected populations, but it seems that the treatment is well tolerated, although it is possibly less effective in this group. HAART in the setting of HCV infection also requires some special consideration, namely an increased incidence of hepatotoxicity. Treatment of co-infected patients requires close monitoring as current therapies are not ideal in terms of effectiveness, and toxicity may be severe.

摘要

自高效抗逆转录病毒疗法(HAART)问世以来,丙型肝炎病毒(HCV)已成为感染人类免疫缺陷病毒(HIV)者发病和死亡的重要因素。HIV的存在显然对HCV的自然病程有负面影响,尽管对于HCV是否影响HIV的自然病程存在一些争议。鉴于合并感染的普遍性以及HCV导致的肝脏损害加速,慢性HCV感染的治疗是HIV合并感染者的一个重要考虑因素。关于聚乙二醇化干扰素和利巴韦林在合并感染人群中的研究较少,但似乎该治疗耐受性良好,尽管在这一群体中可能效果较差。在HCV感染情况下进行HAART也需要一些特殊考虑,即肝毒性发生率增加。合并感染患者的治疗需要密切监测,因为目前的疗法在有效性方面并不理想,而且毒性可能很严重。

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本文引用的文献

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Mortality due to hepatitis C-related liver disease in HIV-infected patients in France (Mortavic 2001 study).法国HIV感染患者中丙型肝炎相关肝病导致的死亡率(Mortavic 2001研究)
AIDS. 2003 Aug 15;17(12):1803-9. doi: 10.1097/00002030-200308150-00009.
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The Delta 32 mutation of the chemokine-receptor 5 gene neither is correlated with chronic hepatitis C nor does it predict response to therapy with interferon-alpha and ribavirin.趋化因子受体5基因的Delta 32突变既与慢性丙型肝炎无关,也不能预测对α干扰素和利巴韦林治疗的反应。
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High frequency of CCR5-delta32 homozygosity in HCV-infected, HIV-1-uninfected hemophiliacs results from resistance to HIV-1.丙型肝炎病毒感染且未感染HIV-1的血友病患者中CCR5-Δ32纯合子的高频率是由对HIV-1的抗性导致的。
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