The impact of currently licensed therapies on viral and immune responses in chronic hepatitis B: Considerations for future novel therapeutics

被引:16
作者
Gill, Upkar S. [1 ]
Kennedy, Patrick T. F. [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Barts Liver Ctr, Blizard Inst, London, England
基金
美国国家卫生研究院; 英国惠康基金;
关键词
hepatitis B surface antigen; NK cells; nucleos(t)ide analogues; pegylated interferon; T cells; TENOFOVIR DISOPROXIL FUMARATE; NATURAL-KILLER-CELLS; CLOSED CIRCULAR DNA; INTERFERON-ALPHA THERAPY; REGULATORY T-CELLS; PEGYLATED-INTERFERON; VIRUS INFECTION; ANTIVIRAL THERAPY; IFN-ALPHA; NK CELLS;
D O I
10.1111/jvh.13040
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Despite the availability of a preventative vaccine, chronic hepatitis B (CHB) remains a global healthcare challenge with the risk of disease progression due to cirrhosis and hepatocellular carcinoma. Although current treatment strategies, interferon and nucleos(t)ide analogues have contributed to reducing morbidity and mortality related to CHB, these therapies are limited in providing functional cure. The treatment paradigm in CHB is rapidly evolving with a number of new agents in the developmental pipeline. However, until novel agents with functional cure capability are available in the clinical setting, there is a pressing need to optimize currently licensed therapies. Here, we discuss current agents used alone and/or in combination strategies along with the impact of these therapies on viral and immune responses. Novel treatment strategies are outlined, and the potential role of current therapies in the employment of pipeline agents is discussed.
引用
收藏
页码:4 / 15
页数:12
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