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Department of Medicine, Department of Biochemistry and Molecular Biology, Jefferson Medical College, Philadelphia, PA 19107
* To whom correspondence should be addressed. Email:
Lance.Simpson{at}jefferson.edu.
Most reports dealing with vaccines against botulinum toxin have focused on the injection route of administration. This is unfortunate, because a mucosal vaccine is likely to be more efficacious for patients and pose fewer risks to health care workers and to the environment. Therefore, efforts were made to generate a mucosal vaccine that would afford protection against the botulinum serotypes that typically cause human illness (A, B, and E). This work demonstrated that carboxyterminal peptides derived from each of the three serotypes possessed the abilities to bind and penetrate human epithelial barriers in vitro, and there was no cross inhibition of membrane binding and transcytosis. The three polypeptides were then tested in vivo as a trivalent vaccine that could be administered to mice by the intranasal route. The results indicated that the mucosal vaccine evoked high secretory titers of IgA, as well as high circulating titers of IgG and IgA, and it also evoked a high level of resistance to challenge with toxin. The immunoglobulin responses and the levels of resistance to challenge were elevated by co-administration of adjuvants, such as chitosan and vitamin E. At least three mechanisms were identified to account for antibody-induced resistance: 1.) blockade of toxin absorption across epithelial cells, 2.) enhanced clearance of toxin from the circulation, and 3.) blockade of toxin action at the neuromuscular junction. These results are a compelling demonstration that a mucosal vaccine against multiple serotypes of botulinum toxin has been identified.
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.
A TRIVALENT VACCINE AGAINST BOTULINUM TOXIN (SEROTYPES A, B AND E) THAT CAN BE ADMINISTERED BY THE MUCOSAL ROUTE
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Abstract
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