The evolution and clinical impact of hepatitis B virus genome diversity
- PMID: 32467580
- DOI: 10.1038/s41575-020-0296-6
The evolution and clinical impact of hepatitis B virus genome diversity
Abstract
The global burden of hepatitis B virus (HBV) is enormous, with 257 million persons chronically infected, resulting in more than 880,000 deaths per year worldwide. HBV exists as nine different genotypes, which differ in disease progression, natural history and response to therapy. HBV is an ancient virus, with the latest reports greatly expanding the host range of the Hepadnaviridae (to include fish and reptiles) and casting new light on the origins and evolution of this viral family. Although there is an effective preventive vaccine, there is no cure for chronic hepatitis B, largely owing to the persistence of a viral minichromosome that is not targeted by current therapies. HBV persistence is also facilitated through aberrant host immune responses, possibly due to the diverse intra-host viral populations that can respond to host-mounted and therapeutic selection pressures. This Review summarizes current knowledge on the influence of HBV diversity on disease progression and treatment response and the potential effect on new HBV therapies in the pipeline. The mechanisms by which HBV diversity can occur both within the individual host and at a population level are also discussed.
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References
-
- Polaris Observatory Collaborators. Global prevalence, treatment, and prevention of hepatitis B virus infection in 2016: a modelling study. Lancet Gastroenterol. Hepatol. 3, 383–403 (2018).
-
- World Health Organization. Global Hepatitis Report, 2019 https://www.who.int/hepatitis/publications/global-hepatitis-report2017/en/ (WHO, 2017).
-
- Parkin, D. M. Global cancer statistics in the year 2000. Lancet Oncol. 2, 533–543 (2001). - PubMed
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