Hiraide Erika, Morinaga Mamiko, Hidaka Hiroki, Yamada Satoki, Takeyama Jun, Kitamura Noriko, Kaminuma Osamu, Hiroi Takachika, Du Weibin, Ohashi-Doi Katsuyo, Nakajima-Adachi Haruyo, Hachimura Satoshi
a Research Center for Food Safety, Graduate School of Agricultural and Life Sciences , The University of Tokyo , Tokyo , Japan.
b Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences , The University of Tokyo , Tokyo , Japan.
Biosci Biotechnol Biochem. 2017 Oct;81(10):1967-1972. doi: 10.1080/09168451.2017.1361806. Epub 2017 Aug 16.
Oral immunotherapy (OIT) is a promising treatment of food allergy. To administer an appropriate oral dose of an allergenic component as OIT to individuals sensitized with a food allergen may prevent inducing food allergic inflammation in them. So we attempted to establish a mouse model to evaluate efficacy for oral administration of food allergen after sensitization. In BALB/c mice sensitized by injecting ovalbumin (OVA) with alum twice, OVA was administered before inducing inflammation by feeding the mice with egg white (EW) diet. Severe inflammatory responses, such as enteropathy, weight loss, IL-4 production, and increase of IgE antibody levels, were suppressed by administration with 4 mg of OVA 7 times before feeding EW diet. OVA administration alone induced a slight Th2 response, but no symptoms. The current study demonstrated that severe food allergic enteropathy could be prevented by pre-administration with appropriate dose of OVA to sensitized mice.