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Epicutaneous allergen application preferentially boosts specific T cell responses in sensitized patients

机译:表皮过敏原的应用优先增强致敏患者的特异性T细胞反应

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摘要

The effects of epicutaneous allergen administration on systemic immune responses in allergic and non-allergic individuals has not been investigated with defined allergen molecules. We studied the effects of epicutaneous administration of rBet v 1 and rBet v 1 fragments on systemic immune responses in allergic and non-allergic subjects. We conducted a clinical trial in which rBet v 1 and two hypoallergenic rBet v 1 fragments were applied epicutaneously by atopy patch testing (APT) to 15 birch pollen (bp) allergic patients suffering from atopic dermatitis, 5 bp-allergic patients suffering from rhinoconjunctivitis only, 5 patients with respiratory allergy without bp allergy and 5 non-allergic individuals. Epicutaneous administration of rBet v 1 and rBet v 1 fragments led to strong and significant increases of allergen-specific T cell proliferation (CLA+ and CCR4+T cell responses) only in bp-allergic patients with a positive APT reaction. There were no relevant changes of Bet v 1-specific IgE and IgG responses. No changes were noted in allergic subjects without bp allergy and in non-allergic subjects. Epicutaneous allergen application boosts specific T cell but not antibody responses mainly in allergic, APT-positive patients suggesting IgE-facilitated allergen presentation as mechanism for its effects on systemic allergen-specific immune responses.
机译:尚未使用确定的过敏原分子研究表皮过敏原对过敏性和非过敏性个体全身免疫应答的影响。我们研究了rBet v 1和rBet v 1片段的表皮给药对变态反应性和非变态反应性受试者的全身免疫反应的影响。我们进行了一项临床试验,其中通过特应性斑贴测试(APT)将rBet v 1和两个低变应原性rBet v 1片段经皮肤应用到15例桦木花粉(bp)过敏性皮炎过敏患者,5 bp过敏性鼻结膜炎患者,5例无bp过敏的呼吸道过敏患者和5例非过敏个体。仅在具有APT反应阳性的bp过敏患者中,对rBet v 1和rBet v 1片段进行表皮给药会导致过敏原特异性T细胞增殖(CLA +和CCR4 + T细胞反应)显着增加。 Bet v 1特异性IgE和IgG响应无相关变化。没有bp过敏的过敏受试者和非过敏受试者均未发现变化。表皮过敏原的应用主要在过敏性APT阳性患者中增强特异性T细胞,但不能增强抗体应答,提示IgE促进过敏原呈递是其对全身性过敏原特异性免疫应答的作用机制。

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