研究者業績
基本情報
研究分野
1論文
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International archives of allergy and immunology 1-6 2023年10月18日BACKGROUND: Allergen-specific immunotherapy (AIT), an established treatment for allergic diseases, prevents the development of other allergic manifestations. Although the mechanisms remain unclear, AIT has been shown to reduce basophil activation (BA) against nontarget allergens. OBJECTIVES: The aim of this study was to assess immunological changes in Dermatophagoides farinae (Der f) after Japanese cedar pollen (JCP)-based subcutaneous immunotherapy (SCIT) monotherapy. METHOD: The data of 16 patients (age: 6-37 years) with JCP-induced allergic rhinitis who were sensitive to Der f (serum Der f-specific immunoglobulin E [IgE] level >0.34 kUA/L) and received JCP-based SCIT for 5 years were reviewed retrospectively. BA by Der f and JCP extracts and serum-specific IgE and immunoglobulin G4 (IgG4) levels against these allergens were evaluated before and after completing 5 years of JCP-based SCIT monotherapy. RESULTS: The areas under the dose-response curves of BA by Der f and JCP extracts were significantly reduced (p = 0.02 and p = 0.002, respectively). JCP-specific IgE levels decreased and JCP-specific IgG4 levels increased significantly (p < 0.001 for both), whereas Der f-specific IgE and IgG4 levels did not change significantly. CONCLUSIONS: JCP-based SCIT monotherapy reduced Der f-specific BA. These findings suggest that JCP-based SCIT has the potential to modulate immune response toward nontarget allergens.
MISC
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アレルギー 56(8-9) 1058-1058 2007年9月
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アレルギー 56(3-4) 396-396 2007年4月
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JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 119(1) S193-S193 2007年1月
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Allergol Int 56(2) 149-155 2007年Background: Phenytoin can induce diversified adverse reactions including generalized eruptions and the hypersensitivity syndrome. Delayed-type allergic mechanisms have been postulated to underlie these reactions. The tests most widely used to detect T-cell sensitization to drugs are the patch test and the lymphocyte transformation test (LTT), but their sensitivity is not sufficient. Simultaneous assessment of both the frequencies and the cytokine-producing phenotypes of allergen-specific T cells has become possible with the recently introduced carboxyfluorescein succinimidyl ester (CFSE) assay.<br> Methods: Seven patients who presented with phenytoin-induced maculopapular exanthema with and without fever were included in this study. Peripheral blood mononuclear cells (PBMCs) were labeled with CFSE and cultured with phenytoin for seven days. The cells were stained with anti-CD4 and cytokine-specific monoclonal antibodies (MoAbs), and analyzed with FACSCalibur.<br> Results: The phenytoin-specific proliferation of CD4+ cells in patients was significantly higher than in the four controls exposed to phenytoin, and in seven healthy children with no previous phenytoin intake. A significant difference in the percentages of CD4+ IFN-γ+ cells between patients and the seven healthy children was observed. The sensitivity and specificity of proliferation were 100% and 90.9%, and those of IFN-γ secretion were 71.4% and 100%, respectively.<br> Conclusions: Phenytoin-specific proliferation may be detected with greater sensitivity by the CFSE dilution assay than the conventional LTT. The assay revealed that both CD4+ and CD4- T cells proliferated and produced IFN-γ and TNF-α after stimulation with phenytoin. The CFSE dilution assay might be useful for the diagnosis and understanding of drug hypersensitivity.<br>
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日本ラテックスアレルギー研究会会誌 10(1) 97-101 2006年12月スギ花粉症とキウイあるいはメロンアレルギーをもつ患者の血清を用い、ELISA inhibitionによってスギ花粉抗原と果物抗原の交差反応部分をIgEが認識しているかどうかを検討した。スギ花粉症と果物アレルギーを合併している9例を対象とした。果物アレルギーの主な症状は口腔アレルギー症状であった。原因果物として多かったのはメロン(7例)とキウイ(6例)であった。これらの血清で、スギ花粉により果物抗原に対するIgE結合能が抑制されるパターとスギ花粉抗原により果物抗原に対するIgE結合能が抑制されないパターンがえられた。交差部位を認識するIgEを持った患者血清を用いてinhibition immunoblotによる検討を行った。メロン抗原とキウイ抗原、いずれの抗原も低分子量タンパク質バンドに対する患者のIgE結合能がスギ抗原の添加により消失している像が見られた。
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JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 117(2) S50-S50 2006年2月
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日本小児アレルギー学会誌 19(4) 684-684 2005年10月
書籍等出版物
1講演・口頭発表等
8共同研究・競争的資金等の研究課題
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日本学術振興会 科学研究費助成事業 2020年4月 - 2025年3月
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日本学術振興会 科学研究費助成事業 2021年4月 - 2024年3月