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DOI 10.1016/j.xcrm.2024.101655

Медицинская библиотека · Cell reports. Medicine · 2024

Development of a hydrogen peroxide-inactivated vaccine that protects against viscerotropic yellow fever in a non-human primate model.

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

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Аннотация

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% (NT50) 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.

Для цитирования: 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. Development of a hydrogen peroxide-inactivated vaccine that protects against viscerotropic yellow fever in a non-human primate model.. Cell reports. Medicine. 2024. DOI: 10.1016/j.xcrm.2024.101655.

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