Hansen Clairissa A, Staples J Erin, Barrett Alan D T
Department of Pathology and Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston, TX, 77555-4036, USA.
Arboviral Diseases Branch, U.S. Centers for Disease Control and Prevention, Fort Collins, CO, USA.
Infect Drug Resist. 2023 Nov 8;16:7141-7154. doi: 10.2147/IDR.S370013. eCollection 2023.
Yellow fever virus (YFV) is a mosquito-borne flavivirus that causes over 109,000 severe infections and over 51,000 deaths annually in endemic areas of sub-Saharan Africa and tropical South America. The virus has a transmission cycle involving mosquitoes and humans or non-human primates (NHPs) as the vertebrate hosts. Although yellow fever (YF) is prevented by a live attenuated vaccine (strain 17D), recent epidemics in Angola, the Democratic Republic of the Congo (DRC), and Brazil put great pressure on vaccine stockpiles. This resulted in the World Health Organization (WHO) and Pan American Health Organization (PAHO) implementing, on an emergency basis only, off-label dose-sparing techniques and policies during 2016-2018 to protect as many people in DRC and Brazil as possible from disease during unexpected large outbreaks of YF. Subsequently non-inferiority studies involving full doses compared to fractional doses indicated promising results, leading some policy-makers and scientists to consider utilizing YF vaccine fractional doses in non-emergency scenarios. Although the additional data on the immunogenicity and safety of fractional doses are promising, there are several questions and considerations that remain regarding the use of fractional doses, including differences in the initial antibody kinetics, differences in the immune response in certain populations, and durability of the immune response to fractional doses compared to full doses. Until the remaining knowledge gaps are addressed, full doses instead of fractional doses should continue to be used unless there are insufficient doses of the vaccine available to control outbreaks of YF.
黄热病病毒(YFV)是一种由蚊子传播的黄病毒,在撒哈拉以南非洲和南美洲热带地区的流行区域,每年导致超过109,000例严重感染和超过51,000例死亡。该病毒具有一个传播循环,涉及蚊子以及作为脊椎动物宿主的人类或非人类灵长类动物(NHP)。尽管黄热病(YF)可通过减毒活疫苗(17D株)预防,但安哥拉、刚果民主共和国(DRC)和巴西近期的疫情给疫苗储备带来了巨大压力。这导致世界卫生组织(WHO)和泛美卫生组织(PAHO)在2016 - 2018年期间仅在紧急情况下实施了超说明书的剂量节省技术和政策,以便在黄热病意外大规模爆发期间尽可能多地保护刚果民主共和国和巴西的民众免受疾病侵害。随后,将全剂量与分剂量进行比较的非劣效性研究显示出了有前景的结果,这使得一些政策制定者和科学家考虑在非紧急情况下使用黄热病疫苗分剂量。尽管关于分剂量免疫原性和安全性的更多数据很有前景,但在分剂量的使用方面仍存在几个问题和需要考虑的因素,包括初始抗体动力学的差异、某些人群免疫反应的差异以及与全剂量相比分剂量免疫反应的持久性。在其余知识空白得到解决之前,除非没有足够的疫苗剂量来控制黄热病疫情,否则应继续使用全剂量而非分剂量。