Review article: hepatitis B—current and emerging therapies. Issue 7 (27th February 2022)

• Record Type: Journal Article
• Authors: Yardeni, David; Ghany, Marc G.
• Is Part Of: Alimentary pharmacology & therapeutics. Volume 55:Issue 7(2022)
• Page Start: 805
• Page End: 819
• Publication Date: 2022-02-27
• Subjects: Digestive organs -- Diseases -- Treatment -- Periodicals; Digestive organs -- Effect of drugs on -- Periodicals; Gastrointestinal system -- Diseases -- Treatment -- Periodicals; Gastrointestinal system -- Effect of drugs on -- Periodicals; 615.73
• DOI: 10.1111/apt.16828
• Languages: English
• ISSNs: 0269-2813

Abstract

Abstract: Background: The hepatitis B virus (HBV) affects an estimated 290 million individuals worldwide and is responsible for approximately 900 000 deaths annually, mostly from complications of cirrhosis and hepatocellular carcinoma. Although current treatment is effective at preventing complications of chronic hepatitis B, it is not curative, and often must be administered long term. There is a need for safe, effective, finite duration curative therapy. Aim: Our aim was to provide a concise, up to date review of all currently available and emerging treatment options for chronic hepatitis B. Methods: We conducted a search of PubMed, clinicaltrials.gov, major meeting abstracts and pharmaceutical websites for publications and communications on current and emerging therapies for HBV. Results: Currently approved treatment options for chronic hepatitis B include peginterferon alpha‐2a and nucleos(t)ide analogues. Both options do not offer a 'complete cure' (clearance of covalently closed circular DNA (cccDNA) and integrated HBV DNA) and rarely achieve a 'functional cure' (hepatitis B surface antigen (HBsAg) loss). An improved understanding of the viral lifecycle, immunopathogenesis and recent advances in drug delivery technologies have led to many novel therapeutic approaches that are currently being evaluated in clinical trials including targeting of viral entry, cccDNA, viral transcription, core protein, and release of HBsAg and HBV polymerase. Additionally, novel immunological approaches that include targeting the innate and adaptive immune system and therapeutic vaccination are being pursued. Conclusion: The breadth and scope of novel therapies in development hold promise for regimen/s that will achieve functional cure. Abstract :