Approaches, Progress, and Challenges to Hepatitis C Vaccine Development

被引:180
作者
Bailey, Justin R. [1 ]
Barnes, Eleanor [2 ,3 ]
Cox, Andrea L. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Infect Dis, 551 Rangos Bldg,855 N Wolfe St, Baltimore, MD 21205 USA
[2] Univ Oxford, Nuffield Dept Med, Peter Medawar Bldg Pathogen Res, Oxford, England
[3] Univ Oxford, Oxford NIHR Biomed Res Ctr, Oxford, England
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
HCV; Viral Hepatitis; Vaccines; Prophylactic Vaccination; T-CELL RESPONSES; HUMAN MONOCLONAL-ANTIBODIES; HYPERVARIABLE REGION 1; BROADLY NEUTRALIZING ANTIBODIES; VIRUS E2 GLYCOPROTEIN; IMMUNE-RESPONSES; VIRAL PERSISTENCE; RHESUS MACAQUES; STRUCTURAL BASIS; SPONTANEOUS CLEARANCE;
D O I
10.1053/j.gastro.2018.08.060
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Risk factors for hepatitis C virus (HCV) infection vary, and there were an estimated 1.75 million new cases worldwide in 2015. The World Health Organization aims for a 90% reduction in new HCV infections by 2030. An HCV vaccine would prevent transmission, regardless of risk factors, and significantly reduce the global burden of HCV-associated disease. Barriers to development include virus diversity, limited models for testing vaccines, and our incomplete understanding of protective immune responses. Although highly effective vaccines could prevent infection altogether, immune responses that increase the rate of HCV clearance and prevent chronic infection may be sufficient to reduce disease burden. Adjuvant envelope or core protein and virus-vectored nonstructural antigen vaccines have been tested in healthy volunteers who are not at risk for HCV infection; viral vectors encoding nonstructural proteins are the only vaccine strategy to be tested in at-risk individuals. Despite development challenges, a prophylactic vaccine is necessary for global control of HCV.
引用
收藏
页码:418 / 430
页数:13
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