| Project/Area Number |
09670881
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Dermatology
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| Research Institution | HIROSHIMA UNIVERSITY |
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Principal Investigator |
HIDE Michihiro Hiroshima University School of Medicine, Department of Dermatology, Research associate, 医学部, 助手 (50284188)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥2,800,000 (Direct Cost: ¥2,800,000)
Fiscal Year 1998: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1997: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | Allergy / The high affinity IgE receptor / Urticaria / Atopic Dermatitis / Autoantibody / Mast cell / Histamine / Transfection / 高親和性IpE受容体 / 蓴麻疹 / アレルギー性鼻炎 |
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| Research Abstract |
In order to analyze histamine releasing autoantibodies in diseases associated with type I allergy performed skin test by autologous sera for patients with chronic urticaria (134), allergic rhinitis (43) atopic dermatitis (70) and healthy controls (114). Fifty-six(42.4%), 0(0%), 3(4.3%) and 2(2.6%) of them showed positive reactions. Serum histamine concentrations of patients with urticaria and those atopic dermatitis were higher than those of healthy controls, but cellular histamine contents were I in patients with urticaria and higher in patients with atopic dermatitis than healthy controls. These results suggested disease specificity of the histamine releasing autoantibodies for urticana and increase of the total amount of cellular and serum histamine in patient with atopic dermatitis. We treated patient with sever chronic urticaria by double diffusion plasmapheresis with reasonable effects. Histamine release test with basophils derived from a healthy volunteer showed sera of approximately 70.4% of the patients with positive skin test by their autologous sera showed apparent histamine releasing activities with predominance of anti-FcepsilonRI type over anti-IgE type activities. In order develop a convenient method for the detection of the autoantibodies, we introduced chimeric FcepsilonRI consisting of human extracellular domain and rat trausmembrane and intracellular domains o receptor into a rat mast cell line (RBL-3D4). The cell line stably expresses the extracellular domain c human FcepsilonRI alpha-subunit and degranulated in response to either anti-FcepsilonRI monoclonal antibody or of patients with chronic urticaria. A pilot screening of the sera of urticaria suggested the cell line is : specific and easy to use than human basophils, but less sensitive. The way of application of this cel for studies of the autoantibodies and the improvement of the sensitivity is a subject for future investigations.
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