Slifka Mark K
Molecular Microbiology and Immunology, Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University , Beaverton, OR , USA.
Front Immunol. 2014 May 6;5:195. doi: 10.3389/fimmu.2014.00195. eCollection 2014.
It is estimated that over 2.5 billion people are at risk for contracting dengue, a virus responsible for 50-390 million infections in addition to thousands of hospitalizations and deaths each year. There are no licensed vaccines available to combat this pathogen but substantial efforts are underway to develop live-attenuated, inactivated, and subunit vaccines that will protect against each of the four serotypes of dengue. Unfortunately, the results of a recent Phase IIb efficacy trial involving a tetravalent live-attenuated chimeric dengue virus vaccine have raised questions with regard to our current understanding of vaccine-mediated immunity to this important flavivirus. Here, we will briefly summarize these vaccination efforts and discuss the importance of informative in vivo models for determining vaccine efficacy and the need to establish a quantitative correlate of immunity in order to predict the duration of vaccine-induced antiviral protection.
据估计,超过25亿人有感染登革热的风险,登革热病毒每年除导致数以千计的住院和死亡外,还造成5亿至3.9亿人感染。目前尚无用于对抗这种病原体的许可疫苗,但正在大力研发减毒活疫苗、灭活疫苗和亚单位疫苗,以预防登革热的四种血清型。不幸的是,最近一项涉及四价减毒活嵌合登革热病毒疫苗的IIb期疗效试验结果,引发了我们对目前对这种重要黄病毒的疫苗介导免疫理解的质疑。在此,我们将简要总结这些疫苗接种工作,并讨论用于确定疫苗疗效的信息丰富的体内模型的重要性,以及建立免疫定量相关指标以预测疫苗诱导的抗病毒保护持续时间的必要性。