Goñi F, Knudsen E, Schreiber F, Scholtzova H, Pankiewicz J, Carp R, Meeker H C, Rubenstein R, Brown D R, Sy M-S, Chabalgoity J A, Sigurdsson E M, Wisniewski T
Department of Neurology, New York University School of Medicine, New York, NY 10016, USA.
Neuroscience. 2005;133(2):413-21. doi: 10.1016/j.neuroscience.2005.02.031.
In recent years major outbreaks of prion disease linked to oral exposure of the prion agent have occurred in animal and human populations. These disorders are associated with a conformational change of a normal protein, PrP(C) (prion protein cellular), to a toxic and infectious form, PrP(Sc) (prion protein scrapie). None of the prionoses currently have an effective treatment. A limited number of active immunization approaches have been shown to slightly prolong the incubation period of prion infection. Active immunization in wild-type animals is hampered by auto-tolerance to PrP and potential toxicity. Here we report that mucosal vaccination with an attenuated Salmonella vaccine strain expressing the mouse PrP, is effective at overcoming tolerance to PrP and leads to a significant delay or prevention of prion disease in mice later exposed orally to the 139A scrapie strain. This mucosal vaccine induced gut anti-PrP immunoglobulin (Ig)A and systemic anti-PrP IgG. No toxicity was evident with this vaccination approach. This promising finding suggests that mucosal vaccination may be a useful method for overcoming tolerance to PrP and preventing prion infection among animal and potentially human populations at risk.
近年来,与朊病毒因子经口暴露相关的朊病毒病在动物和人类群体中发生了重大疫情。这些疾病与正常蛋白质PrP(C)(细胞朊蛋白)的构象变化有关,转变为有毒且具有传染性的形式PrP(Sc)(瘙痒病朊蛋白)。目前,尚无有效的治疗方法来治疗任何朊病毒病。有限数量的主动免疫方法已被证明可略微延长朊病毒感染的潜伏期。野生型动物的主动免疫受到对PrP的自身耐受性和潜在毒性的阻碍。在此,我们报告用表达小鼠PrP的减毒沙门氏菌疫苗株进行黏膜疫苗接种,可有效克服对PrP的耐受性,并显著延迟或预防随后经口暴露于139A瘙痒病株的小鼠发生朊病毒病。这种黏膜疫苗诱导肠道抗PrP免疫球蛋白(Ig)A和全身性抗PrP IgG。这种疫苗接种方法未显示出明显的毒性。这一有前景的发现表明,黏膜疫苗接种可能是一种有用的方法,可用于克服对PrP的耐受性,并在有风险的动物群体乃至人类群体中预防朊病毒感染。