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食物中的变应原模拟表位会增强小鼠的I型过敏反应。

Allergen mimotopes in food enhance type I allergic reactions in mice.

作者信息

Jensen-Jarolim E, Wiedermann U, Ganglberger E, Zurcher A, Stadler B M, Boltz-Nitulescu G, Scheiner O, Breiteneder H

机构信息

Department of General and Experimental Pathology, University of Vienna, 1090 Vienna, Austria.

出版信息

FASEB J. 1999 Sep;13(12):1586-92. doi: 10.1096/fasebj.13.12.1586.

Abstract

BIP1is a murine IgG antibody capable of enhancing the IgE binding to Bet v 1, the major birch pollen allergen. We have previously generated a mimotope of BIP1, designated Bet mim 1, from a constrained phage display peptide library. We demonstrated that oral immunization of BALB/c mice with the Bet mim 1 mimotope resulted in the induction of Bet v 1-specific IgG. The aim of this study was to test the influence of such an oral immunization with Bet mim 1 on a subsequent type I allergic response to Bet v 1. Phages displaying Bet mim 1 or control mimotopes, or PBS alone, were delivered to BALB/c mice by intragastric gavages prior to systemic sensitization with recombinant Bet v 1 and Al(OH)(3), an adjuvant inducing preferentially IgE antibody responses. Only mice fed with Bet mim 1-phages displayed substantially enhanced type I allergic skin reactivity to Bet v 1, as compared to mice pretreated with control mimotopes or PBS. A gastric digestion assay indicated that Bet v 1 and its homologue from apple, Mal d 1, were degraded within seconds under physiological conditions. In contrast, phage-displayed mimotopes were resistant to digestion. Our data indicate that allergen mimics in the diet that resist digestion, can induce allergen specific IgG able to enhance an allergic response. We therefore conclude that sensitization via the oral route may represent a mechanism for aggravating type I allergic reactions, probably leading to an earlier onset of symptoms even at lower allergen dosage.

摘要

BIP1是一种鼠源IgG抗体,能够增强IgE与桦树花粉主要过敏原Bet v 1的结合。我们之前从一个受限的噬菌体展示肽库中筛选出了BIP1的模拟表位,命名为Bet mim 1。我们证明用Bet mim 1模拟表位口服免疫BALB/c小鼠可诱导产生Bet v 1特异性IgG。本研究的目的是测试用Bet mim 1进行这种口服免疫对随后针对Bet v 1的I型过敏反应的影响。在用重组Bet v 1和Al(OH)₃(一种优先诱导IgE抗体反应的佐剂)进行全身致敏之前,通过胃内灌胃将展示Bet mim 1或对照模拟表位的噬菌体,或仅用PBS递送至BALB/c小鼠。与用对照模拟表位或PBS预处理的小鼠相比,仅喂食Bet mim 1噬菌体的小鼠对Bet v 1的I型过敏皮肤反应性显著增强。胃消化试验表明,Bet v 1及其苹果同源物Mal d 1在生理条件下几秒钟内就会被降解。相比之下,噬菌体展示的模拟表位对消化具有抗性。我们的数据表明,饮食中抗消化的过敏原模拟物可诱导能够增强过敏反应的过敏原特异性IgG。因此,我们得出结论,经口致敏可能是加重I型过敏反应的一种机制,甚至可能在较低过敏原剂量下导致症状更早出现。

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