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Smallpox DNA Vaccine Protects Nonhuman Primates against Lethal Monkeypox

机译:天花DNA疫苗可保护非人类灵长类动物免受致命的猴痘危害

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摘要

Two decades after a worldwide vaccination campaign was used to successfully eradicate naturally occurring smallpox, the threat of bioterrorism has led to renewed vaccination programs. In addition, sporadic outbreaks of human monkeypox in Africa and a recent outbreak of human monkeypox in the U.S. have made it clear that naturally occurring zoonotic orthopoxvirus diseases remain a public health concern. Much of the threat posed by orthopoxviruses could be eliminated by vaccination; however, because the smallpox vaccine is a live orthopoxvirus vaccine (vaccinia virus) administered to the skin, the vaccine itself can pose a serious health risk. Here, we demonstrate that rhesus macaques vaccinated with a DNA vaccine consisting of four vaccinia virus genes (L1R, A27L, A33R, and B5R) were protected from severe disease after an otherwise lethal challenge with monkeypox virus. Animals vaccinated with a single gene (L1R) which encodes a target of neutralizing antibodies developed severe disease but survived. This is the first demonstration that a subunit vaccine approach to smallpox-monkeypox immunization is feasible.
机译:在全球疫苗接种运动成功消灭天然天花的二十年后,生物恐怖主义的威胁导致了新的疫苗接种计划。另外,在非洲零星爆发的人类猴痘和最近在美国爆发的人类猴痘清楚地表明,自然发生的人畜共患正痘病毒疾病仍然是公共卫生问题。疫苗可以消除正痘病毒造成的大部分威胁;但是,由于天花疫苗是一种活的正痘病毒疫苗(牛痘病毒),可以接种到皮肤上,因此疫苗本身会带来严重的健康风险。在这里,我们证明接种了由四个痘苗病毒基因(L1R,A27L,A33R和B5R)组成的DNA疫苗的恒河猴猕猴受到了致命的攻击,受到了猴痘病毒的致命攻击。用编码中和抗体靶标的单一基因(L1R)接种的动物发展为严重疾病,但存活了下来。这是第一个证明亚单位疫苗用于天花-猴痘免疫的方法是可行的。

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