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Targeting Innate and Adaptive Immune Responses to Cure Chronic HBV Infection
被引:129
|作者:
Gehring, Adam J.
[1
,2
,3
]
Protzer, Ulrike
[4
,5
]
机构:
[1] Univ Hlth Network, Toronto Ctr Liver Dis, Toronto, ON, Canada
[2] Univ Hlth Network, Toronto Gen Hosp, Res Inst, Toronto, ON, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[4] Tech Univ Munich, Inst Virol, Helmholtz Zentrum Munchen, Munich, Germany
[5] German Ctr Infect Res DZIF, Munich Partnersite, Munich, Germany
基金:
欧盟地平线“2020”;
关键词:
Drug;
HBsAg;
Vaccine;
Inflammation;
HEPATITIS-B-VIRUS;
CD8(+) T-CELLS;
ADOPTIVE TRANSFER;
VIRAL-HEPATITIS;
SURFACE-ANTIGEN;
HEPATOCELLULAR-CARCINOMA;
PROGRAMMED DEATH-1;
LIVER;
REPLICATION;
HEPATOCYTES;
D O I:
10.1053/j.gastro.2018.10.032
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Fewer than 1% of chronic hepatitis B virus infections per year are cured with antiviral treatment. This creates a need for long-term treatment, which poses challenges for patients and health systems. Because cure is accompanied by recovery of antiviral immunity, a combination of direct-acting antiviral agents and immunotherapy are likely to be required. Extensive efforts have been made to identify determinants of the failed immune response to hepatitis B virus in patients with chronic infection. We review mechanisms of immune dysfunction in patients with chronic hepatitis B virus infection, immunotherapy strategies in development, and the challenges associated with successful implementation of immunotherapy.
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页码:325 / 337
页数:13
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