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Host functions used by hepatitis B virus to complete its life cycle: Implications for developing host-targeting agents to treat chronic hepatitis B.
- Source :
-
Antiviral research [Antiviral Res] 2018 Oct; Vol. 158, pp. 185-198. Date of Electronic Publication: 2018 Aug 24. - Publication Year :
- 2018
-
Abstract
- Similar to other mammalian viruses, the life cycle of hepatitis B virus (HBV) is heavily dependent upon and regulated by cellular (host) functions. These cellular functions can be generally placed in to two categories: (a) intrinsic host restriction factors and innate defenses, which must be evaded or repressed by the virus; and (b) gene products that provide functions necessary for the virus to complete its life cycle. Some of these functions may apply to all viruses, but some may be specific to HBV. In certain cases, the virus may depend upon the host function much more than does the host itself. Knowing which host functions regulate the different steps of a virus' life cycle, can lead to new antiviral targets and help in developing novel treatment strategies, in addition to improving a fundamental understanding of viral pathogenesis. Therefore, in this review we will discuss known host factors which influence key steps of HBV life cycle, and further elucidate therapeutic interventions targeting host-HBV interactions.<br /> (Copyright © 2018. Published by Elsevier B.V.)
- Subjects :
- Animals
Capsid metabolism
DNA, Viral
Hepatitis B virus genetics
Hepatitis B virus pathogenicity
Hepatocytes drug effects
Hepatocytes virology
Host-Pathogen Interactions genetics
Humans
Life Cycle Stages
Liver virology
Nucleocapsid
Reverse Transcription drug effects
Viral Envelope Proteins metabolism
Virus Assembly physiology
Virus Attachment
Virus Internalization drug effects
Virus Replication
Antiviral Agents pharmacology
Hepatitis B drug therapy
Hepatitis B virus drug effects
Hepatitis B virus physiology
Host-Pathogen Interactions drug effects
Host-Pathogen Interactions physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-9096
- Volume :
- 158
- Database :
- MEDLINE
- Journal :
- Antiviral research
- Publication Type :
- Academic Journal
- Accession number :
- 30145242
- Full Text :
- https://doi.org/10.1016/j.antiviral.2018.08.014