Graham Barney S
Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, United States.
Curr Opin Virol. 2017 Apr;23:107-112. doi: 10.1016/j.coviro.2017.03.012. Epub 2017 May 16.
Respiratory syncytial virus (RSV) is an important and ubiquitous respiratory pathogen for which no vaccine is available notwithstanding more than 50 years of effort. It causes the most severe disease at the extremes of age and in settings of immunodeficiency. Although RSV is susceptible to neutralizing antibody, it has evolved multiple mechanisms of immune evasion allowing it to repeatedly infect people despite relatively little genetic diversity. Recent breakthroughs in determining the structure and antigenic content of the fusion (F) glycoprotein in its metastable untriggered prefusion form (pre-F) and the stable rearranged postfusion form (post-F) have yielded vaccine strategies that can induce potent neutralizing antibody responses and effectively boost pre-existing neutralizing activity. In parallel, novel live-attenuated and chimeric virus vaccine candidates and other novel approaches to deliver vaccine antigens have been developed. These events and activities have aroused optimism and a robust pipeline of potential vaccine products that promise to provide a means to reduce the public health burden of RSV infection.
呼吸道合胞病毒(RSV)是一种重要且普遍存在的呼吸道病原体,尽管经过50多年的努力,仍没有可用的疫苗。它在年龄极端情况下和免疫缺陷环境中会引发最严重的疾病。虽然RSV对中和抗体敏感,但它已经进化出多种免疫逃逸机制,使其尽管遗传多样性相对较少,仍能反复感染人类。最近在确定融合(F)糖蛋白处于亚稳态未触发前融合形式(前F)和稳定重排后融合形式(后F)的结构和抗原内容方面取得的突破,产生了能够诱导强效中和抗体反应并有效增强预先存在的中和活性的疫苗策略。与此同时,新型减毒活疫苗和嵌合病毒候选疫苗以及其他递送疫苗抗原的新方法也已开发出来。这些事件和活动引发了人们的乐观情绪,以及一系列有望提供减轻RSV感染公共卫生负担手段的潜在疫苗产品。