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Hepatitis C.

作者信息

Webster Daniel P, Klenerman Paul, Dusheiko Geoffrey M

机构信息

Department of Virology, Royal Free London NHS Foundation Trust, London, UK.

National Institute for Health Research (NIHR) Biomedical Research Centre and Nuffield Department of Medicine, University of Oxford, Oxford, UK.

出版信息

Lancet. 2015 Mar 21;385(9973):1124-35. doi: 10.1016/S0140-6736(14)62401-6. Epub 2015 Feb 14.


DOI:10.1016/S0140-6736(14)62401-6
PMID:25687730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4878852/
Abstract

Hepatitis C virus (HCV) infection is a major health problem worldwide. The effects of chronic infection include cirrhosis, end-stage liver disease, and hepatocellular carcinoma. As a result of shared routes of transmission, co-infection with HIV is a substantial problem, and individuals infected with both viruses have poorer outcomes than do peers infected with one virus. No effective vaccine exists, although persistent HCV infection is potentially curable. The standard of care has been subcutaneous interferon alfa and oral ribavirin for 24-72 weeks. This treatment results in a sustained virological response in around 50% of individuals, and is complicated by clinically significant adverse events. In the past 10 years, advances in HCV cell culture have enabled an improved understanding of HCV virology, which has led to development of many new direct-acting antiviral drugs that target key components of virus replication. These direct-acting drugs allow for simplified and shortened treatments for HCV that can be given as oral regimens with increased tolerability and efficacy than interferon and ribavirin. Remaining obstacles include access to appropriate care and treatment, and development of a vaccine.

摘要

相似文献

[1]
Hepatitis C.

Lancet. 2015-3-21

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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本文引用的文献

[1]
All-oral 12-week treatment with daclatasvir plus sofosbuvir in patients with hepatitis C virus genotype 3 infection: ALLY-3 phase III study.

Hepatology. 2015-4

[2]
Efficacy and safety of 12 weeks versus 18 weeks of treatment with grazoprevir (MK-5172) and elbasvir (MK-8742) with or without ribavirin for hepatitis C virus genotype 1 infection in previously untreated patients with cirrhosis and patients with previous null response with or without cirrhosis (C-WORTHY): a randomised, open-label phase 2 trial.

Lancet. 2014-11-11

[3]
Sofosbuvir plus ribavirin for the treatment of chronic genotype 4 hepatitis C virus infection in patients of Egyptian ancestry.

J Hepatol. 2014-11-5

[4]
An interferon-free antiviral regimen for HCV after liver transplantation.

N Engl J Med. 2014-11-11

[5]
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Gastroenterology. 2014-10-7

[6]
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Gastroenterology. 2014-9-28

[7]
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Lancet. 2014-7-28

[8]
All-oral daclatasvir plus asunaprevir for hepatitis C virus genotype 1b: a multinational, phase 3, multicohort study.

Lancet. 2014-7-28

[9]
Sofosbuvir and ribavirin for hepatitis C in patients with HIV coinfection.

JAMA. 2014

[10]
Simeprevir with pegylated interferon alfa 2a plus ribavirin in treatment-naive patients with chronic hepatitis C virus genotype 1 infection (QUEST-1): a phase 3, randomised, double-blind, placebo-controlled trial.

Lancet. 2014-6-4

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