Hepatitis B virus: new therapeutic perspectives. (January 2016)
- Record Type:
- Journal Article
- Title:
- Hepatitis B virus: new therapeutic perspectives. (January 2016)
- Main Title:
- Hepatitis B virus: new therapeutic perspectives
- Authors:
- Lin, Chih‐Lin
Yang, Hung‐Chih
Kao, Jia‐Horng - Abstract:
- Abstract: Current antiviral therapies have dramatically improved the long‐term outcomes of patients with chronic hepatitis B virus (HBV) infection. Both interferon (IFN) and nucleos(t)ide analogue (NA) treatments have been shown to reduce the progression of liver disease in chronic hepatitis B (CHB) patients. However, persistent covalently closed circular DNA (cccDNA) can result in a viral relapse after discontinuation of antiviral treatment. On the basis of extensive research on the HBV lifecycle and virus–host interactions, several new agents focusing on viral and host targets are under development to cure HBV. New polymerase inhibitors, tenofovir alafenamide and besifovir provide effective and safer treatment for CHB patients. Agents targeting cccDNA, such as engineered site‐specific nucleases and RNA interference therapeutics could eliminate cccDNA or silence cccDNA transcription. Inhibitors of HBV nucleocapsid assembly suppress capsid formation and prevent synthesis of HBV DNA. The HBV entry inhibitor, Myrcludex‐B, has been shown to effectively inhibit amplification of cccDNA as well as the spread of intrahepatic infection. Agents targeting host factors that enhance innate and adaptive immune responses, including the lymphotoxin‐β receptor agonist, toll‐like receptor agonist, immune checkpoint inhibitors and adenovirus‐based therapeutic vaccine, could play a critical role in the elimination of HBV‐infected cells. With all of these promising approaches, we hope to reachAbstract: Current antiviral therapies have dramatically improved the long‐term outcomes of patients with chronic hepatitis B virus (HBV) infection. Both interferon (IFN) and nucleos(t)ide analogue (NA) treatments have been shown to reduce the progression of liver disease in chronic hepatitis B (CHB) patients. However, persistent covalently closed circular DNA (cccDNA) can result in a viral relapse after discontinuation of antiviral treatment. On the basis of extensive research on the HBV lifecycle and virus–host interactions, several new agents focusing on viral and host targets are under development to cure HBV. New polymerase inhibitors, tenofovir alafenamide and besifovir provide effective and safer treatment for CHB patients. Agents targeting cccDNA, such as engineered site‐specific nucleases and RNA interference therapeutics could eliminate cccDNA or silence cccDNA transcription. Inhibitors of HBV nucleocapsid assembly suppress capsid formation and prevent synthesis of HBV DNA. The HBV entry inhibitor, Myrcludex‐B, has been shown to effectively inhibit amplification of cccDNA as well as the spread of intrahepatic infection. Agents targeting host factors that enhance innate and adaptive immune responses, including the lymphotoxin‐β receptor agonist, toll‐like receptor agonist, immune checkpoint inhibitors and adenovirus‐based therapeutic vaccine, could play a critical role in the elimination of HBV‐infected cells. With all of these promising approaches, we hope to reach the ultimate goal of a cure to HBV in the near future. … (more)
- Is Part Of:
- Liver international. Volume 36:Number 1(2016)Supplement
- Journal:
- Liver international
- Issue:
- Volume 36:Number 1(2016)Supplement
- Issue Display:
- Volume 36, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 36
- Issue:
- 1
- Issue Sort Value:
- 2016-0036-0001-0000
- Page Start:
- 85
- Page End:
- 92
- Publication Date:
- 2016-01
- Subjects:
- chronic hepatitis B -- covalently closed circular DNA -- hepatitis B virus
Liver -- Periodicals
Liver -- Diseases -- Periodicals
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1478-3231 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/liv.13003 ↗
- Languages:
- English
- ISSNs:
- 1478-3223
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5280.514000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1924.xml