Author
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VAN REGENMORTEL, M-H - INST DE BIOLOGIE, FRANCE |
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GUICHARD, G - INST DE BIOLOGIE, FRANCE |
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BENKIRANE, N - INST DE BIOLOGIE, FRANCE |
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BRIAND, J-P - INST DE BIOLOGIE, FRANCE |
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MULLER, S - INST DE BIOLOGIE, FRANCE |
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Brown, Fred |
Submitted to: Developments in Biological Standardization
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 7/13/1997 Publication Date: N/A Citation: N/A Interpretive Summary: The potential of peptides as immunogens has been the subject of much research during the past two decades, since the methods for nucleic acid sequencing became available. This technology has been used extensively in FMD research and a peptide corresponding to the major immunogenic site on the virus particle has been shown to elicit protective levels of neutralizing antibodies in experimental animals and susceptible species. In an extension of this work, the concept of using peptides synthesized from D-amino acids has been explored. The results with the immunogenic peptide of FMDV are highly encouraging. Technical Abstract: Retro-inverso (RI) peptides, also called all-D-retro peptides, have been shown to mimic the antigenic and immunogenic properties of L-peptides successfully. RI peptides corresponding to the loop 141-159 of the VP1 protein of FMDV have been synthesized and used to immunize rabbits and guinea pigs. These peptides induced longer-lasting and higher antibody titers in immunized animals than did the corresponding L-peptides and the antibodies cross-reacted strongly with virus particles and with L-peptides. Antisera raised to RI peptides had in vitro virus neutralization titres equal to or better than those obtained after immunization with classical FMDV antigens and L-peptides. In view of their increased stability, RI peptides may overcome some of the shortcomings of synthetic viral vaccines based on L-peptides. |