Kong Leopold, Jackson Kelli N, Wilson Ian A, Law Mansun
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037, USA.
Curr Opin Virol. 2015 Apr;11:148-57. doi: 10.1016/j.coviro.2015.04.001. Epub 2015 Apr 29.
Hepatitis C virus infects nearly 3% of the world's population and is often referred as a silent epidemic. It is a leading cause of liver cirrhosis and hepatocellular carcinoma in endemic countries. Although antiviral drugs are now available, they are not readily accessible to marginalized social groups and developing nations that are disproportionally impacted by HCV. To stop the HCV pandemic, a vaccine is needed. Recent advances in HCV research have provided new opportunities for studying HCV neutralizing antibodies and their subsequent use for rational vaccine design. It is now recognized that neutralizing antibodies to conserved antigenic sites of the virus can cross-neutralize diverse HCV genotypes and protect against infection in vivo. Structural characterization of the neutralizing epitopes has provided valuable information for design of candidate immunogens.
丙型肝炎病毒感染了全球近3%的人口,常被称为一种隐匿性流行病。在流行国家,它是肝硬化和肝细胞癌的主要病因。尽管现在已有抗病毒药物,但边缘化社会群体和受丙型肝炎病毒影响尤为严重的发展中国家却难以获得这些药物。为了阻止丙型肝炎病毒大流行,需要一种疫苗。丙型肝炎病毒研究的最新进展为研究丙型肝炎病毒中和抗体及其随后用于合理的疫苗设计提供了新机会。现在人们认识到,针对病毒保守抗原位点的中和抗体可以交叉中和多种丙型肝炎病毒基因型,并在体内预防感染。中和表位的结构表征为候选免疫原的设计提供了有价值的信息。