Amanna Ian J, Thomas Archana, Engelmann Flora, Hammarlund Erika, Raué Hans-Peter, Bailey Adam L, Poore Elizabeth A, Quintel Benjamin K, Lewis Anne D, Axthelm Michael K, Johnson Amanda L, Colgin Lois M A, Diamond Michael S, Messaoudi Ilhem, Slifka Mark K
Najít Technologies, Inc., Beaverton, OR 97006, USA.
Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.
Cell Rep Med. 2024 Jul 16;5(7):101655. doi: 10.1016/j.xcrm.2024.101655.
Yellow fever virus (YFV) is endemic in >40 countries and causes viscerotropic disease with up to 20%-60% mortality. Successful live-attenuated yellow fever (YF) vaccines were developed in the mid-1930s, but their use is restricted or formally contraindicated in vulnerable populations including infants, the elderly, and people with compromised immune systems. In these studies, we describe the development of a next-generation hydrogen peroxide-inactivated YF vaccine and determine immune correlates of protection based on log neutralizing index (LNI) and neutralizing titer-50% (NT) studies. In addition, we compare neutralizing antibody responses and protective efficacy of hydrogen peroxide-inactivated YF vaccine candidates to live-attenuated YFV-17D (YF-VAX) in a rhesus macaque model of viscerotropic YF. Our results indicate that an optimized, inactivated YF vaccine elicits protective antibody responses that prevent viral dissemination and lethal infection in rhesus macaques and may be a suitable alternative for vaccinating vulnerable populations who are not eligible to receive replicating live-attenuated YF vaccines.
黄热病病毒(YFV)在40多个国家呈地方性流行,可引发内脏型疾病,死亡率高达20% - 60%。20世纪30年代中期研制出了成功的减毒活黄热病(YF)疫苗,但在包括婴儿、老年人和免疫系统受损者在内的易感人群中,其使用受到限制或被正式列为禁忌。在这些研究中,我们描述了下一代过氧化氢灭活YF疫苗的研发过程,并基于对数中和指数(LNI)和中和滴度50%(NT)研究确定了保护的免疫相关性。此外,我们在恒河猴内脏型YF模型中比较了过氧化氢灭活YF疫苗候选株与减毒活YFV - 17D(YF - VAX)的中和抗体反应和保护效力。我们的结果表明,一种优化的灭活YF疫苗能引发保护性抗体反应,可防止恒河猴体内病毒传播和致死性感染,对于那些没有资格接种可复制的减毒活YF疫苗的易感人群,它可能是一种合适的替代疫苗。