Jonker Emile F F, Visser Leonardus G, Roukens Anna H
Department of Infectious Diseases, Leiden University Medical Center, Leiden, the Netherlands.
Department of Infectious Diseases C5-P, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, the Netherlands.
Ther Adv Vaccines. 2013 Nov;1(4):144-52. doi: 10.1177/2051013613498954.
Ever since its development in 1937, the live-attenuated 17D yellow fever (YF) vaccine has been one of the most effective vaccines available to man. In this review we highlight the major steps in the development of 17D YF vaccine. We discuss the use of neutralizing antibodies as a surrogate marker for protection, and explore the strengths and weaknesses of the current plaque reduction neutralization test (PRNT), a technique developed in the 1960s that continues to be superior to every modern test in both sensitivity and specificity. The neutralizing antibodies demonstrated by the PRNT can be detected for several decades after vaccination, possibly even for the remainder of the recipient's natural life. We review the available evidence on the duration of protection after primary vaccination, a topic that has been the subject of controversy over the last few months. For persons who are immunocompromised due to disease, medication or advancing age, the duration of protection may be shorter: they should always have their vaccine response checked by PRNT. Due to the higher risk of severe adverse events after vaccination with 17D YF in this group, the development of a new, inactivated vaccine will have substantial benefits in this population.
自1937年研发以来,减毒活17D黄热病(YF)疫苗一直是人类可获得的最有效疫苗之一。在本综述中,我们重点介绍17D YF疫苗研发的主要步骤。我们讨论了使用中和抗体作为保护的替代标志物,并探讨了当前蚀斑减少中和试验(PRNT)的优缺点,该技术于20世纪60年代开发,在灵敏度和特异性方面仍然优于所有现代试验。PRNT显示的中和抗体在接种疫苗后几十年都能检测到,甚至可能在受种者的余生中都能检测到。我们回顾了关于初次接种疫苗后保护持续时间的现有证据,这一话题在过去几个月一直存在争议。对于因疾病、药物治疗或年龄增长而免疫功能低下的人,保护持续时间可能较短:他们应始终通过PRNT检查疫苗反应。由于该群体接种17D YF疫苗后发生严重不良事件的风险较高,开发一种新的灭活疫苗将给这一人群带来巨大益处。