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Transcriptomic assay of CD8+ T cells in treatment-naïve HIV, HCV-mono-infected and HIV/HCV-co-infected Chinese.中国治疗初治 HIV、HCV 单感染和 HIV/HCV 共感染患者的 CD8+T 细胞的转录组分析。
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Impaired hepatitis C virus (HCV)-specific interferon-γ responses in individuals with HIV who acquire HCV infection: correlation with CD4(+) T-cell counts.在感染 HCV 的 HIV 个体中,丙型肝炎病毒 (HCV)-特异性干扰素-γ 反应受损:与 CD4(+) T 细胞计数相关。
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Chronic immune activation is a distinguishing feature of liver and PBMC gene signatures from HCV/HIV coinfected patients and may contribute to hepatic fibrogenesis.慢性免疫激活是 HCV/HIV 合并感染患者肝和 PBMC 基因特征的一个显著特征,可能导致肝纤维化。
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Differential regulation of the Let-7 family of microRNAs in CD4+ T cells alters IL-10 expression.Let-7 家族 microRNAs 在 CD4+ T 细胞中的差异调控改变了 IL-10 的表达。
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An update on treatment of genotype 1 chronic hepatitis C virus infection: 2011 practice guideline by the American Association for the Study of Liver Diseases.1型慢性丙型肝炎病毒感染治疗的最新进展:美国肝病研究协会2011年实践指南
Hepatology. 2011 Oct;54(4):1433-44. doi: 10.1002/hep.24641. Epub 2011 Sep 26.
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Hepatitis C virus infection and hepatic stellate cell activation downregulate miR-29: miR-29 overexpression reduces hepatitis C viral abundance in culture.丙型肝炎病毒感染和肝星状细胞激活下调 miR-29:miR-29 过表达可降低培养中的丙型肝炎病毒载量。
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丙型肝炎病毒与1型人类免疫缺陷病毒合并感染

Hepatitis C Virus and HIV Type 1 Co-Infection.

作者信息

Gupta Priyanka

机构信息

Retroviral Genetics Division, Centre for Virus Research, Westmead Millennium Institute , Sydney, Australia.

出版信息

Infect Dis Rep. 2013 Jun 6;5(Suppl 1):e7. doi: 10.4081/idr.2013.s1.e7.

DOI:10.4081/idr.2013.s1.e7
PMID:24470971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3892626/
Abstract

Around 33 million people worldwide are living with Human Immunodeficiency Virus (HIV) infection, and approximately 20-30% of HIV-infected individuals are also infected with Hepatitis C virus (HCV). The main form of HCV transmission is via the blood borne route; high rates of co-infection are found in intravenous drug users with HCV prevalence rates as high as 90%. Introduction of effective antiretroviral therapy (ART) has led to a significant decline in HIV-related morbidity, but at the same time the incidence of HCV related liver disease is increasing in the co-infected population. Meta analysis has revealed that individuals who are co-infected with HIV/HCV harbor three times greater risk of progression to liver disease than those infected with HCV alone. Increased risk of progression to Acquired Immunodeficiency Syndrome (AIDS) and AIDS-related deaths is shown among the co-infected patients by some studies, suggesting that HCV infection may accelerate the clinical course of HIV infection. HCV may also affect the incidence of liver toxicity associated with ART, affecting the management of HIV infection. There is a lack of optimal therapeutic approaches to treat HCV infection in HIV co-infected patients. This review discusses recent literature pertaining HIV/HCV co-infection, in addition to providing a snapshot of impact of co-infection on human genome at the level of gene expression and its regulation by microRNAs (miRNAs).

摘要

全球约有3300万人感染了人类免疫缺陷病毒(HIV),约20%-30%的HIV感染者同时感染了丙型肝炎病毒(HCV)。HCV的主要传播途径是经血传播;静脉吸毒者中的合并感染率很高,HCV患病率高达90%。有效的抗逆转录病毒疗法(ART)的引入使HIV相关发病率显著下降,但与此同时,合并感染人群中HCV相关肝病的发病率正在上升。荟萃分析表明,HIV/HCV合并感染的个体发展为肝病的风险是单纯感染HCV个体的三倍。一些研究显示,合并感染患者发展为获得性免疫缺陷综合征(AIDS)和AIDS相关死亡的风险增加,这表明HCV感染可能会加速HIV感染的临床进程。HCV还可能影响与ART相关的肝毒性发生率,从而影响HIV感染的管理。目前缺乏针对HIV合并感染患者HCV感染的最佳治疗方法。本综述讨论了有关HIV/HCV合并感染的最新文献,此外还概述了合并感染在基因表达水平对人类基因组以及微小RNA(miRNA)对其调控的影响。