Mucosal vaccination delays or prevents prion infection via an oral route

被引:80
作者
Goñi, F
Knudsen, E
Schreiber, F
Scholtzova, H
Pankiewicz, J
Carp, R
Meeker, HC
Rubenstein, R
Brown, DR
Sy, MS
Chabalgoity, JA
Sigurdsson, EM
Wisniewski, T
机构
[1] NYU, Sch Med, Millhauser Lab, Dept Neurol, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Psychiat, New York, NY 10016 USA
[4] New York State Inst Basic Res Dev Disabil, Staten Isl, NY 10314 USA
[5] Suny Downstate Med Ctr, Dept Biochem, Brooklyn, NY 11203 USA
[6] Univ Bath, Dept Biol, Bath BA2 7AY, Avon, England
[7] Univ Bath, Dept Biochem, Bath BA2 7AY, Avon, England
[8] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
[9] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
[10] Univ Uruguay, Fac Med, Lab Vaccine Res, Dept Biotechnol,Inst Higiene, Montevideo, Uruguay
[11] Univ Uruguay, Sch Chem, Dept Immunol, Montevideo, Uruguay
关键词
scraple; immunization; Salmonella vaccine strain; Creutzfeldt-Jakob disease; bovine spongiform encephalopathy; chronic wasting disease;
D O I
10.1016/j.neuroscience.2005.02.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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, PrPc (prion protein cellular), to a toxic and infectious form, PrPSc (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. (c) 2005 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:413 / 421
页数:9
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