کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3421695 1226670 2016 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Control and Eradication Strategies of Hepatitis B Virus
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی میکروب شناسی
پیش نمایش صفحه اول مقاله
Control and Eradication Strategies of Hepatitis B Virus
چکیده انگلیسی

Hepatitis B virus (HBV) is a major human pathogen, and chronic hepatitis can lead to cirrhosis and malignant hepatocellular carcinoma. While HBV vaccine and treatment are available, it has remained a challenge to completely eradicate the virus from patients. Current therapy using either interferon or polymerase inhibitors cannot cure HBV with a high efficacy. Lifelong therapy is needed to suppress HBV in patients who achieve no seroconversion. Here, we review recent exciting advances of new strategies, including the inhibition of viral entry, the destruction or silencing of HBV covalently closed circular DNA (cccDNA), and breaking immune tolerance. Combinations of different therapeutic strategies could improve the cure rate of viral persistence in chronic hepatitis B.

TrendsTwo major causes of chronic infection with hepatitis B virus (HBV) are the persistence of HBV covalently closed DNA (cccDNA) in the nucleus of hepatocytes, and local immune tolerance in the HBV-infected liver.A highly active research area has been in entry inhibition of HBV infection by entry inhibitors.Eradication of cccDNA by the CRISPR/Cas9 approach has been attempted in a number of recent reports.Vigorous research in immunotherapy for HBV persistence would rejuvenate host immunity and restore HBV-specific T cells to an effective level.Clinical trials with immunotherapy are ongoing, including treatments with an anti-PD-1 antibody, ligands for various kinds of Toll-like receptors, and therapeutic vaccination.Combinations of various therapeutic approaches could shed new light on the interruption of disease progression and, ultimately, prevent end-stage liver diseases.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: - Volume 24, Issue 9, September 2016, Pages 739–749
نویسندگان
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