Hepatitis B virus infection

被引:1789
作者
Trepo, Christian [1 ,2 ]
Chan, Henry L. Y. [3 ,4 ]
Lok, Anna [5 ]
机构
[1] Hosp Civils Lyon, Croix Rousse Hosp, Dept Hepatol, Lyon, France
[2] INSERM U1052, Lyon, France
[3] Chinese Univ Hong Kong, Inst Digest Dis, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, State Key Lab Digest Dis, Hong Kong, Hong Kong, Peoples R China
[5] Univ Michigan Hlth Syst, Div Gastroenterol & Hepatol, Ann Arbor, MI USA
基金
美国国家卫生研究院;
关键词
E-ANTIGEN SEROCONVERSION; TENOFOVIR DISOPROXIL FUMARATE; HBEAG-POSITIVE PATIENTS; SURFACE-ANTIGEN; HEPATOCELLULAR-CARCINOMA; NATURAL-HISTORY; FOLLOW-UP; ALANINE AMINOTRANSFERASE; PEGINTERFERON ALPHA-2A; HBSAG SEROCLEARANCE;
D O I
10.1016/S0140-6736(14)60220-8
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
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.
引用
收藏
页码:2053 / 2063
页数:11
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