病毒学
病毒
脑炎
生物
兽医病毒学
α病毒
类病毒颗粒
委内瑞拉马脑炎病毒
医学
遗传学
重组DNA
基因
作者
Sung‐Youl Ko,Wataru Akahata,Eun Sung Yang,Wing‐Pui Kong,Crystal W. Burke,Shelley P. Honnold,Donald K. Nichols,Yan‐Jang S. Huang,Gretchen L. Schieber,Kevin Carlton,Luis DaSilva,Vicki Traina‐Dorge,Dana L. Vanlandingham,Yaroslav Tsybovsky,Tyler Stephens,Ulrich Baxa,Stephen Higgs,Chad J. Roy,Pamela J. Glass,John R. Mascola
标识
DOI:10.1126/scitranslmed.aav3113
摘要
Western, Eastern, and Venezuelan equine encephalitis viruses (WEEV, EEEV, and VEEV, respectively) are important mosquito-borne agents that pose public health and bioterrorism threats. Despite considerable advances in understanding alphavirus replication, there are currently no available effective vaccines or antiviral treatments against these highly lethal pathogens. To develop a potential countermeasure for viral encephalitis, we generated a trivalent, or three-component, EEV vaccine composed of virus-like particles (VLPs). Monovalent VLPs elicited neutralizing antibody responses and protected mice and nonhuman primates (NHPs) against homologous challenges, but they were not cross-protective. In contrast, NHPs immunized with trivalent VLPs were completely protected against aerosol challenge by each of these three EEVs. Passive transfer of IgG from immunized NHPs protected mice against aerosolized EEV challenge, demonstrating that the mechanism of protection was humoral. Because they are replication incompetent, these trivalent VLPs represent a potentially safe and effective vaccine that can protect against diverse encephalitis viruses.
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