Project/Area Number |
26870244
|
Research Category |
Grant-in-Aid for Young Scientists (B)
|
Allocation Type | Multi-year Fund |
Research Field |
Collagenous pathology/Allergology
Pediatrics
|
Research Institution | Gifu University |
Principal Investigator |
Kawamoto Norio 岐阜大学, 医学部附属病院, 助教 (50397337)
|
Project Period (FY) |
2014-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
Keywords | 経口免疫療法 / カゼイン |
Outline of Final Research Achievements |
IgE-mediated reactions are risk of oral immunotherapy (OIT), while T cell reactions seem to be necessary for desensitization. We developed novel hydrolyzed casein, which is designed to digest IgE epitopes and can induce a lymphocyte response and performed the OIT. Thirteen participants with cow's milk allergy were enrolled, and ten have been successively increased the threshold for casein after escalation phase. Cytokines produced from peripheral mononuclear cell stimulated by casein were measured comprehensively by bead-based multiple-proteins quantification system. We used the samples of tree time points consisted by before the escalation phase, after the escalation phase and after the maintenance phase. We could observe no significant difference in these cytokines. However, IL-4/IL-12(p70) ratio showed significant decrease according to the time course, indicating the possible shift toward to Th1 from Th2. Further investigation may needed with larger population.
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