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本文引用的文献

1
A novel small molecule inhibitor of hepatitis C virus entry.一种新型丙型肝炎病毒进入抑制剂。
PLoS Pathog. 2010 Sep 2;6(9):e1001086. doi: 10.1371/journal.ppat.1001086.
2
Diagnosis of occult hepatitis C without the need for a liver biopsy.无需肝活检即可诊断隐匿性丙型肝炎。
J Med Virol. 2010 Sep;82(9):1554-9. doi: 10.1002/jmv.21866.
3
Hepatitis C: viral and host factors associated with non-response to pegylated interferon plus ribavirin.丙型肝炎:聚乙二醇干扰素联合利巴韦林治疗无应答的病毒和宿主因素。
Liver Int. 2010 Oct;30(9):1259-69. doi: 10.1111/j.1478-3231.2010.02283.x.
4
Social networks shape the transmission dynamics of hepatitis C virus.社交网络影响丙型肝炎病毒的传播动态。
PLoS One. 2010 Jun 23;5(6):e11170. doi: 10.1371/journal.pone.0011170.
5
Review article: specifically targeted anti-viral therapy for hepatitis C - a new era in therapy.综述文章:针对丙型肝炎的特异性抗病毒治疗 - 治疗新时代。
Aliment Pharmacol Ther. 2010 Jul;32(1):14-28. doi: 10.1111/j.1365-2036.2010.04317.x. Epub 2010 Mar 31.
6
Oyster mushroom laccase inhibits hepatitis C virus entry into peripheral blood cells and hepatoma cells.平菇漆酶可抑制丙型肝炎病毒进入外周血细胞和肝癌细胞。
Protein Pept Lett. 2010 Aug;17(8):1031-9. doi: 10.2174/092986610791498948.
7
High antibody level: an accurate serologic marker of viremia in asymptomatic people with hepatitis C infection.高抗体水平:丙型肝炎感染无症状个体病毒血症的准确血清学标志物。
Transfusion. 2010 Jun;50(6):1335-43. doi: 10.1111/j.1537-2995.2009.02571.x. Epub 2010 Jan 15.
8
Proanthocyanidin from blueberry leaves suppresses expression of subgenomic hepatitis C virus RNA.蓝莓叶中的原花青素可抑制丙型肝炎病毒亚基因组RNA的表达。
J Biol Chem. 2009 Aug 7;284(32):21165-76. doi: 10.1074/jbc.M109.004945. Epub 2009 Jun 16.
9
A study of best positive predictors for sustained virologic response to interferon alpha plus ribavirin therapy in naive chronic hepatitis C patients.初治慢性丙型肝炎患者对干扰素α加利巴韦林治疗持续病毒学应答的最佳阳性预测指标研究。
BMC Gastroenterol. 2009 Jan 20;9:5. doi: 10.1186/1471-230X-9-5.
10
New therapies for hepatitis C virus infection.丙型肝炎病毒感染的新疗法。
Clin Infect Dis. 2009 Feb 1;48(3):313-20. doi: 10.1086/595848.

丙型肝炎治疗:现状和未来展望。

Hepatitis C treatment: current and future perspectives.

机构信息

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

出版信息

Virol J. 2010 Nov 1;7:296. doi: 10.1186/1743-422X-7-296.

DOI:10.1186/1743-422X-7-296
PMID:21040548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2984595/
Abstract

Hepatitis C virus (HCV) is a member of Flaviviridae family and one of the major causes of liver disease. There are about 175 million HCV infected patients worldwide that constitute 3% of world's population. The main route of HCV transmission is parental however 90% intravenous drug users are at highest risk. Standard interferon and ribavirin remained a gold standard of chronic HCV treatment having 38-43% sustained virological response rates. Currently the standard therapy for HCV is pegylated interferon (PEG-INF) with ribavirin. This therapy achieves 50% sustained virological response (SVR) for genotype 1 and 80% for genotype 2 & 3. As pegylated interferon is expensive, standard interferon is still the main therapy for HCV treatment in under developed countries. On the other hand, studies showed that pegylated IFN and RBV therapy has severe side effects like hematological complications. Herbal medicines (laccase, proanthocyandin, Rhodiola kirilowii) are also being in use as a natural and alternative way for treatment of HCV but there is not a single significant report documented yet. Best SVR indicators are genotype 3 and 2, < 0.2 million IU/mL pretreatment viral load, rapid virological response (RVR) rate and age <40 years. New therapeutic approaches are under study like interferon related systems, modified forms of ribavirin, internal ribosome entry site (HCV IRES) inhibitors, NS3 and NS5a inhibitors, novel immunomodulators and specifically targeted anti-viral therapy for hepatitis C compounds. More remedial therapies include caspase inhibitors, anti-fibrotic agents, antibody treatment and vaccines.

摘要

丙型肝炎病毒 (HCV) 是黄病毒科的一员,也是导致肝脏疾病的主要原因之一。全球约有 1.75 亿 HCV 感染者,占世界人口的 3%。HCV 的主要传播途径是母婴传播,但 90%的静脉吸毒者风险最高。标准干扰素和利巴韦林仍然是慢性 HCV 治疗的金标准,持续病毒学应答率为 38-43%。目前,HCV 的标准治疗是聚乙二醇干扰素 (PEG-INF) 联合利巴韦林。这种治疗方法对基因型 1 的持续病毒学应答率为 50%(SVR),对基因型 2 和 3 的 SVR 率为 80%。由于聚乙二醇干扰素价格昂贵,标准干扰素仍然是发展中国家治疗 HCV 的主要药物。另一方面,研究表明,聚乙二醇干扰素和利巴韦林治疗有严重的副作用,如血液学并发症。草药(漆酶、原花青素、红景天)也被用作 HCV 治疗的天然和替代方法,但目前还没有一份有意义的报告记录在案。最佳 SVR 指标是基因型 3 和 2、治疗前病毒载量<0.2 百万 IU/mL、快速病毒学应答 (RVR) 率和年龄<40 岁。正在研究新的治疗方法,如干扰素相关系统、改良的利巴韦林形式、内部核糖体进入位点 (HCV IRES) 抑制剂、NS3 和 NS5a 抑制剂、新型免疫调节剂和针对丙型肝炎化合物的特异性靶向抗病毒治疗。更多的治疗方法包括半胱天冬酶抑制剂、抗纤维化药物、抗体治疗和疫苗。