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皮内免疫疗法通过完整的皮肤使树突状细胞快速摄取过敏原,并下调致敏小鼠的过敏原特异性反应。

Epicutaneous immunotherapy results in rapid allergen uptake by dendritic cells through intact skin and downregulates the allergen-specific response in sensitized mice.

机构信息

DBV Technologies, Pépinière Paris Santé Cochin, 75014 Paris, France.

出版信息

J Immunol. 2011 May 15;186(10):5629-37. doi: 10.4049/jimmunol.1003134. Epub 2011 Apr 13.

Abstract

Epicutaneous immunotherapy onto intact skin has proved to be an efficient and safe alternative treatment of allergy in an animal model with various allergens and in children for cow's milk allergy. The aim of this study was to analyze the different steps of the immunological handling of the allergen when deposited on intact skin using an epicutaneous delivery system and its immune consequences in sensitized BALB/c mice. As expected, when applied on intact skin, OVA exhibits neither a passive passage through the skin nor any detectable systemic delivery. The current study demonstrates that, after a prolonged application on intact skin, OVA is taken up by dendritic cells in the superficial layers of the stratum corneum and transported, after internalization, to the draining lymph nodes, with variations according to the previous level of sensitization of the mice. When OVA is applied with the epicutaneous delivery system repeatedly, specific local and systemic responses are down-modulated in association with the induction of regulatory T cells. Besides providing new insights into skin function in the presence of allergens, this study indicates that the skin might have a tolerogenic role, at least when kept intact.

摘要

经皮免疫疗法已被证明是一种有效的、安全的替代疗法,可以治疗动物模型中的各种过敏原和儿童的牛奶过敏症。本研究的目的是分析在致敏 BALB/c 小鼠中,使用经皮给药系统将过敏原沉积在完整皮肤表面时,其免疫处理的不同步骤及其免疫后果。正如预期的那样,当应用于完整皮肤时,OVA 既不会被动通过皮肤,也不会有任何可检测到的全身递送。本研究表明,在完整皮肤表面长时间应用后,OVA 被角质层浅层的树突状细胞摄取,并在内化后被运送到引流淋巴结,其变化取决于小鼠先前的致敏水平。当 OVA 与经皮给药系统重复应用时,特异性局部和全身反应会被下调,同时诱导调节性 T 细胞。除了为过敏原存在时的皮肤功能提供新的见解外,本研究还表明,皮肤至少在保持完整时可能具有耐受作用。

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