Hepatitis B virus infection
Journal Title: | The Lancet (British edition) 2014, Vol.384 (9959), p.2053-2063 |
Main Author: | Trépo, Christian, Prof |
Other Authors: | Chan, Henry L Y, Prof , Lok, Anna, Prof |
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English |
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Quelle: | Alma/SFX Local Collection |
Publisher: | Kidlington: Elsevier Ltd |
ID: | ISSN: 0140-6736 |
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recordid: | cdi_proquest_miscellaneous_1661621212 |
title: | Hepatitis B virus infection |
format: | Article |
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ispartof: | The Lancet (British edition), 2014, Vol.384 (9959), p.2053-2063 |
description: | Summary Hepatitis B virus infection is a major public health problem worldwide; roughly 30% of the world's population show serological evidence of current or past infection. Hepatitis B virus is a partly double-stranded DNA virus with several serological markers: HBsAg and anti-HBs, HBeAg and anti-HBe, and anti-HBc IgM and IgG. It is transmitted through contact with infected blood and semen. A safe and effective vaccine has been available since 1981, and, although variable, the implementation of universal vaccination in infants has resulted in a sharp decline in prevalence. Hepatitis B virus is not cytopathic; both liver damage and viral control—and therefore clinical outcome—depend on the complex interplay between virus replication and host immune response. Overall, as much as 40% of men and 15% of women with perinatally acquired hepatitis B virus infection will die of liver cirrhosis or hepatocellular carcinoma. In addition to decreasing hepatic inflammation, long-term antiviral treatment can reverse cirrhosis and reduce hepatocellular carcinoma. Development of new therapies that can improve HBsAg clearance and virological cure is warranted. |
language: | eng |
source: | Alma/SFX Local Collection |
identifier: | ISSN: 0140-6736 |
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