Aiming for Functional Cure With Established and Novel Therapies for Chronic Hepatitis B

被引:31
作者
Choi, Hannah S. J. [1 ]
Tonthat, Alexander [2 ]
Janssen, Harry L. A. [1 ]
Terrault, Norah A. [2 ]
机构
[1] Toronto Gen Hosp, Toronto Ctr Liver Dis, Toronto, ON, Canada
[2] Univ Southern Calif, Keck Sch Med, 1450 San Pablo Ave HC4 Room 3054, Los Angeles, CA 90033 USA
关键词
PEGYLATED INTERFERON ALPHA-2A; TENOFOVIR DISOPROXIL FUMARATE; REVERSE-TRANSCRIPTASE INHIBITOR; NUCLEOS(T)IDE ANALOG THERAPY; HBEAG-NEGATIVE PATIENTS; CHRONIC HBV INFECTION; SURFACE-ANTIGEN; OPEN-LABEL; ALANINE AMINOTRANSFERASE; NATURAL-HISTORY;
D O I
10.1002/hep4.1875
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Chronic hepatitis B virus (HBV) infection remains difficult to cure due to the persistent, self-replenishing nature of the viral genome and impaired host immune responses. Current treatment goals for chronic hepatitis B (CHB) are to prevent or significantly delay liver-related adverse outcomes and death, and two types of treatments are available: nucleos(t)ide analogues (NAs) and interferons (IFNs). NAs effectively suppress HBV replication, and IFNs improve serological response rates, thereby decreasing the risk of adverse outcomes. However, their efficacy in attaining serological responses, especially functional cure (i.e., loss of serum hepatitis B surface antigen), is very limited. Various strategies such as stopping antiviral therapy or combining therapies have been investigated to enhance response, but efficacy is only modestly improved. Importantly, the development of novel direct-acting antivirals and immunomodulators is underway to improve treatment efficacy and enhance rates of functional cure. The present review provides an overview of the treatment goals and indications, the possibility of expanding indications, and the safety and efficacy of different treatment strategies involving established and/or novel therapies as we continue our search for a cure.
引用
收藏
页码:935 / 949
页数:15
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