Affiliation:
1. Department of Biochemistry, Imperial College of Science,Technology and Medicine, London SW7 2Z, UK
Abstract
Mammals have evolved a sophisticated immune system for handling antigens encountered at their mucosal surfaces. The way in which mucosally delivered antigens are handled influences our ability to design effective mucosal vaccines. Live attenuated derivatives of pathogens are one route towards the development of mucosal vaccines. However, some molecules, described as mucosal immunogens, are inherently immunogenic at mucosal surfaces. Studies on mucosal immunogens may facilitate the identification of common characteristics that contribute to mucosal immunogenicity and aid the development of novel, non–living mucosal vaccines and immunostimulators.
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Reference45 articles.
1. Adjuvanticity of the cholera toxin A1-based gene fusion protein, CTA1-DD, is critically dependent on the ADP-ribosyltransferase and Ig-binding activity;Agren L. C.;J. Immunol.,1999
2. Oral vaccination: identi¢cation of classes of proteins that provoke an immune response upon oral feeding;Aizapurua D. H.;J. Exp. Med.,1988
3. Interactions between stromal cell--derived keratinocyte growth factor and epithelial transforming growth factor in immune-mediated crypt cell hyperplasia.
4. A common mucosal immunological system involving the bronchus, breast and bowel;Bienenstock J.;Adv. Exp. Med. Biol.,1978
5. Coster T. S. (and 10 others) 1999 Vaccination against shigellosis with attenuated Shigella £exneri 2a strain SC602. Infect. Immun. 67 3437^3443.
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