Hepatitis B
- PMID: 36774930
- DOI: 10.1016/S0140-6736(22)01468-4
Hepatitis B
Abstract
Hepatitis B virus (HBV) infection is a major public health problem, with an estimated 296 million people chronically infected and 820 000 deaths worldwide in 2019. Diagnosis of HBV infection requires serological testing for HBsAg and for acute infection additional testing for IgM hepatitis B core antibody (IgM anti-HBc, for the window period when neither HBsAg nor anti-HBs is detected). Assessment of HBV replication status to guide treatment decisions involves testing for HBV DNA, whereas assessment of liver disease activity and staging is mainly based on aminotransferases, platelet count, and elastography. Universal infant immunisation, including birth dose vaccination is the most effective means to prevent chronic HBV infection. Two vaccines with improved immunogenicity have recently been approved for adults in the USA and EU, with availability expected to expand. Current therapies, pegylated interferon, and nucleos(t)ide analogues can prevent development of cirrhosis and hepatocellular carcinoma, but do not eradicate the virus and rarely clear HBsAg. Treatment is recommended for patients with cirrhosis or with high HBV DNA levels and active or advanced liver disease. New antiviral and immunomodulatory therapies aiming to achieve functional cure (ie, clearance of HBsAg) are in clinical development. Improved vaccination coverage, increased screening, diagnosis and linkage to care, development of curative therapies, and removal of stigma are important in achieving WHO's goal of eliminating HBV infection by 2030.
Copyright © 2023 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests W-JJ has served as advisor and lecturer for Bristol Myers Squibb and Gilead; and received grants for research and attendance of meetings from Chang Gung Medical Foundation and National Science Council of Taiwan. GVP has served as advisor and lecturer for Amgen, Gilead, GlaxoSmithKline, Ipsen, Janssen, Novo Nordisk, Roche, and Takeda; received support for attendance of meetings from Gilead Sciences, Ipsen, Janssen, Merck Sharp & Dohme, Novo Nordisk, Roche, and Takeda; and received research grants from Gilead. ASFL has received research grants from Bristol Myers Squibb, Gilead, and TARGET Pharma, and royalties from Wolters Kluwer (UpToDate) and Wiley (textbooks); and served as advisor and consultant for Ambys, Amgen, Arbutus, Chroma, CLEAR-B, Eli Lilly, Enanta, Enochian, GlaxoSmithKline, GNI, Huahui, Janssen, TARGET, and Virion. Editorial note: the Lancet Group takes a neutral position with respect to territorial claims in published maps and institutional affiliations.
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