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Live Attenuated Francisella novicida Vaccine Protects against Francisella tularensis Pulmonary Challenge in Rats and Non-human Primates

机译:减毒活新弗朗西斯菌疫苗可预防大鼠和非人类灵长类动物对兔弗朗西斯菌的肺部攻击。

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Francisella tularensis causes the disease tularemia. Human pulmonary exposure to the most virulent form, F. tularensis subsp. tularensis (Ftt), leads to high morbidity and mortality, resulting in this bacterium being classified as a potential biothreat agent. However, a closely-related species, F. novicida, is avirulent in healthy humans. No tularemia vaccine is currently approved for human use. We demonstrate that a single dose vaccine of a live attenuated F. novicida strain (Fn iglD) protects against subsequent pulmonary challenge with Ftt using two different animal models, Fischer 344 rats and cynomolgus macaques (NHP). The Fn iglD vaccine showed protective efficacy in rats, as did a Ftt iglD vaccine, suggesting no disadvantage to utilizing the low human virulent Francisella species to induce protective immunity. Comparison of specific antibody profiles in vaccinated rat and NHP sera by proteome array identified a core set of immunodominant antigens in vaccinated animals. This is the first report of a defined live attenuated vaccine that demonstrates efficacy against pulmonary tularemia in a NHP, and indicates that the low human virulence F. novicida functions as an effective tularemia vaccine platform.
机译:图拉弗朗西斯菌引起了图拉血病。人肺暴露于最强毒的形式F. tularensis亚种。 tularensis(Ftt)导致较高的发病率和死亡率,导致该细菌被分类为潜在的生物威胁因子。但是,在健康的人类中,一种紧密相关的物种No. F. novicida是无毒的。目前尚未批准将妥拉血病疫苗用于人类。我们证明了减毒活的诺维达菌株(Fn iglD)的单剂疫苗可防止使用两种不同的动物模型,即Fischer 344大鼠和食蟹猕猴(NHP)用Ftt预防随后的肺部攻击。 Fn iglD疫苗与Ftt iglD疫苗一样,在大鼠中表现出保护作用,这表明利用人类低毒力弗氏杆菌物种诱导保护性免疫没有缺点。通过蛋白质组学阵列比较接种的大鼠和NHP血清中的特异性抗体谱,从而确定了接种动物中的一组免疫优势抗原。这是确定的减毒活疫苗的首次报道,该疫苗在NHP中显示出抗肺部Tularemia的功效,并表明低人类毒力No. Novicida可作为有效的Tularemia疫苗平台。

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