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

被引:2
作者
Amanna, Ian J. [1 ]
Thomas, Archana [2 ]
Engelmann, Flora [3 ]
Hammarlund, Erika [2 ]
Raue, Hans-Peter [2 ]
Bailey, Adam L. [4 ]
Poore, Elizabeth A. [1 ]
Quintel, Benjamin K. [1 ]
Lewis, Anne D. [5 ]
Axthelm, Michael K. [6 ,7 ]
Johnson, Amanda L. [5 ]
Colgin, Lois M. A. [5 ]
Diamond, Michael S. [8 ,9 ,10 ]
Messaoudi, Ilhem [3 ]
Slifka, Mark K. [2 ]
机构
[1] Najit Technol Inc, Beaverton, OR 97006 USA
[2] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Div Neurosci, Beaverton, OR 97006 USA
[3] Univ Kentucky, Coll Med, Dept Microbiol Immunol & Mol Genet, Lexington, KY 40506 USA
[4] Univ Wisconsin Madison, Dept Pathol & Lab Med, Madison, WI 53706 USA
[5] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Div Comparat Med, Beaverton, OR 97006 USA
[6] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Div Pathobiol & Immunol, Beaverton, OR 97006 USA
[7] Oregon Hlth & Sci Univ, Vaccine & Gene Therapy Inst, Beaverton, OR 97006 USA
[8] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[9] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[10] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
ADVERSE EVENTS; VIRUS; 17D; SAFETY; IMMUNOGENICITY; IMMUNIZATION; IMMUNITY; LIVE; ANTIBODIES; CHALLENGE;
D O I
10.1016/j.xcrm.2024.101655
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 liveattenuated 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.
引用
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页数:23
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