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Effect of Cry-consensus Peptide, a Novel Recombinant Peptide for Immunotherapy of Japanese Cedar Pollinosis, on an Experimental Allergic Rhinitis Model in B10.S Mice

Authors :
Kohsuke Kino
Daisuke Kozutsumi
Masako Tsunematsu
Shigeki Kimura
Taketo Yamaji
Rika Murakami
Source :
Allergology International, Vol 56, Iss 4, Pp 465-472 (2007)
Publisher :
Japanese Society of Allergology. Production and hosting by Elsevier B.V.

Abstract

Background We are developing an immunotherapeutic peptide, Cry-consensus peptide, for Japanese cedar pollinosis. Cry-consensus peptide is a recombinant polypeptide containing six major human T-cell epitopes derived from both Cry j 1 and Cry j 2, two major allergens of Japanese cedar pollen. We examined the effect of Cry-consensus peptide on an allergic rhinitis model in B10.S mice, which have one common T-cell epitope in the Cry-consensus peptide. Methods B10.S mice were sensitized with Cry j 1/alum, then the Cry-consensus peptide was administered subcutaneously once a week for 5 weeks from the last sensitization. Histamine was dropped in both nostrils (10 μL per nostril) of each mouse on the day before continuous intranasal instillation of Cry j 1. Soon after the final challenge with Cry j 1, the mice were observed for 5 minutes for the resulting number of sneezes. In addition, serum levels of Cry j 1-specific IgE and IgG2a antibody, eosinophil infiltration in nasal tissue, and Cry j 1- specific cytokine production from splenocytes were evaluated. Results Cry-consensus peptide markedly inhibited Cry j 1-induced sneezes, eosinophil infiltration, and eosinophil peroxidase (EPO) activity in nasal tissue. Cry-consensus peptide inhibited the production of anti-Cry j 1 IgE (Th2-mediated) and significantly enhanced anti-Cry j 1 IgG2a (Th1-mediated). In cytokine production from splenocytes, Cry-consensus peptide significantly decreased in IL-4/IFN-γ and IL-5/IFN-γ ratios. Conclusions It was concluded that Cry-consensus peptide effectively controlled allergic responses, which results from shifting from a Th2-dominated to a Th1-dominated immune response.

Details

Language :
English
ISSN :
13238930
Issue :
4
Database :
OpenAIRE
Journal :
Allergology International
Accession number :
edsair.doi.dedup.....12bb3a17b9406ca9d67506f3eda5a580
Full Text :
https://doi.org/10.2332/allergolint.O-07-495