期刊
GASTROENTEROLOGY
卷 156, 期 2, 页码 369-383出版社
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2018.08.061
关键词
Hepatitis B Virus; Hepatitis C Virus; Immune Memory; Innate
资金
- National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
- Deutsche Forschungsgemeinschaft [TRR 179, SFB 1160 IMPATH]
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [ZIADK054508, ZIADK054516, ZIADK054509] Funding Source: NIH RePORTER
There are 257 million persons worldwide with chronic hepatitis B virus (HBV) infection, a leading causes of liver cancer. Almost all adults with acute HBV infection have a rapid immune response to the virus, resulting in life-long immunity, but there is no cure for individuals with chronic HBV infection, which they acquire during early life. The mechanisms that drive the progression of HBV through distinct clinical phases to end-stage liver disease are poorly understood. Likewise, it is not clear whether and how immune responses can be modulated to allow control and/or clearance of intrahepatic HBV DNA. We review the innate and adaptive immune responses to acute and chronic HBV infections and responses to antiviral therapy. Comparisons with hepatitis C virus infection provide insights into the reversibility of innate inflammatory responses and the potential for successful therapy to recover virus-specific memory immune responses.
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