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An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein

BACKGROUND: Rice is commonly known as a staple crop consumed worldwide, though with several rice proteins being reported for allergic properties in clinical studies. Thus, there is a growing need for the development of an animal model to better understand the allergenicity of rice proteins and the i...

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Autores principales: Chen, Xiao-Wei, Lau, Ken Wan-Keung, Yang, Fan, Sun, Samuel Sai-Ming, Fung, Ming-Chiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123647/
https://www.ncbi.nlm.nih.gov/pubmed/21605393
http://dx.doi.org/10.1186/1471-230X-11-62
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author Chen, Xiao-Wei
Lau, Ken Wan-Keung
Yang, Fan
Sun, Samuel Sai-Ming
Fung, Ming-Chiu
author_facet Chen, Xiao-Wei
Lau, Ken Wan-Keung
Yang, Fan
Sun, Samuel Sai-Ming
Fung, Ming-Chiu
author_sort Chen, Xiao-Wei
collection PubMed
description BACKGROUND: Rice is commonly known as a staple crop consumed worldwide, though with several rice proteins being reported for allergic properties in clinical studies. Thus, there is a growing need for the development of an animal model to better understand the allergenicity of rice proteins and the immunological and pathophysiological mechanisms underlying the development of food allergy. METHODS: Groups of BALB/c mice were sensitized daily with freshly homogenized rice flour (30 mg or 80 mg) without adjuvant by intragastric gavage. In addition, the mice were challenged with extracted rice flour proteins at several time points intragastrically. Hypersensitivity symptoms in mice were evaluated according to a scoring system. Vascular leakage, ELISA of rice protein-specific IgE, histopathology of small intestine, and passive cutaneous anaphylaxis were conducted on challenged mice. RESULTS: An adjuvant free mouse model of rice allergy was established with sensitized mice showing increased scratching behaviors and increased vascular permeability. Rice protein-specific IgE was detected after eighteen days of sensitization and from the fifth challenge onwards. Inflammatory damage to the epithelium in the small intestine of mice was observed beyond one month of sensitization. Passive cutaneous anaphylaxis results confirmed the positive rice allergy in the mouse model. CONCLUSIONS: We introduced a BALB/c mouse model of rice allergy with simple oral sensitization without the use of adjuvant. This model would serve as a useful tool for further analysis on the immunopathogenic mechanisms of the various rice allergens, for the evaluation of the hypersensitivity of rice or other cereal grains, and to serve as a platform for the development of immunotherapies against rice allergens.
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spelling pubmed-31236472011-06-26 An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein Chen, Xiao-Wei Lau, Ken Wan-Keung Yang, Fan Sun, Samuel Sai-Ming Fung, Ming-Chiu BMC Gastroenterol Research Article BACKGROUND: Rice is commonly known as a staple crop consumed worldwide, though with several rice proteins being reported for allergic properties in clinical studies. Thus, there is a growing need for the development of an animal model to better understand the allergenicity of rice proteins and the immunological and pathophysiological mechanisms underlying the development of food allergy. METHODS: Groups of BALB/c mice were sensitized daily with freshly homogenized rice flour (30 mg or 80 mg) without adjuvant by intragastric gavage. In addition, the mice were challenged with extracted rice flour proteins at several time points intragastrically. Hypersensitivity symptoms in mice were evaluated according to a scoring system. Vascular leakage, ELISA of rice protein-specific IgE, histopathology of small intestine, and passive cutaneous anaphylaxis were conducted on challenged mice. RESULTS: An adjuvant free mouse model of rice allergy was established with sensitized mice showing increased scratching behaviors and increased vascular permeability. Rice protein-specific IgE was detected after eighteen days of sensitization and from the fifth challenge onwards. Inflammatory damage to the epithelium in the small intestine of mice was observed beyond one month of sensitization. Passive cutaneous anaphylaxis results confirmed the positive rice allergy in the mouse model. CONCLUSIONS: We introduced a BALB/c mouse model of rice allergy with simple oral sensitization without the use of adjuvant. This model would serve as a useful tool for further analysis on the immunopathogenic mechanisms of the various rice allergens, for the evaluation of the hypersensitivity of rice or other cereal grains, and to serve as a platform for the development of immunotherapies against rice allergens. BioMed Central 2011-05-23 /pmc/articles/PMC3123647/ /pubmed/21605393 http://dx.doi.org/10.1186/1471-230X-11-62 Text en Copyright ©2011 Chen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Xiao-Wei
Lau, Ken Wan-Keung
Yang, Fan
Sun, Samuel Sai-Ming
Fung, Ming-Chiu
An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
title An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
title_full An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
title_fullStr An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
title_full_unstemmed An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
title_short An adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
title_sort adjuvant free mouse model of oral allergenic sensitization to rice seeds protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123647/
https://www.ncbi.nlm.nih.gov/pubmed/21605393
http://dx.doi.org/10.1186/1471-230X-11-62
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