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β-乳球蛋白连续B细胞表位的识别模式不会因牛奶过敏的临床表现而有所不同。

The recognition pattern of sequential B cell epitopes of beta-lactoglobulin does not vary with the clinical manifestations of cow's milk allergy.

作者信息

Heinzmann A, Blattmann S, Spuergin P, Forster J, Deichmann K A

机构信息

University Children's Hospital, University of Freiburg, Freiburg, Germany.

出版信息

Int Arch Allergy Immunol. 1999 Dec;120(4):280-6. doi: 10.1159/000024280.

Abstract

BACKGROUND

beta-Lactoglobulin (BLG) represents one of the major allergens causing cow's milk allergy (CMA) - a disease with a wide spectrum of clinical symptoms. The aim of this study was to evaluate sequential B cell epitopes of BLG by the Pin-ELISA method. Furthermore, we wanted to investigate a possible association of the IgE recognition patterns in sera of patients with BLG sensitization and the type of clinical reactions following contact with cow's milk.

METHODS

Overlapping sequential decapeptides corresponding to the amino acid sequence of BLG were used in Pin-ELISAs specific for human IgE. Tested sera were from 14 individuals with CMA, 8 of them with a history of immediate systemic reactions and 6 with delayed skin reactions following contact with cow's milk. All of them showed specific IgE antibodies to BLG in the CAP-RAST. Control sera were from 5 healthy nonallergic individuals.

RESULTS

All sera from BLG-sensitized individuals showed IgE binding with one region of BLG corresponding to amino acids 95-113. Furthermore, individual sera showed reactions with two further regions, 12-27 and 124-135. Inhibition of IgE binding to BLG with one soluble synthetic peptide confirmed the major epitope. No differences were found in the B cell epitope recognition pattern to BLG in the two groups of patients with CMA, characterized by acute systemic or delayed skin reactions.

CONCLUSIONS

Using IgE Pin-ELISAs we were able to confirm previously described sequential B cell epitopes of BLG. However, the recognition pattern of one of the major cow's milk allergens is not predictive of the clinical type of reaction.

摘要

背景

β-乳球蛋白(BLG)是引起牛奶过敏(CMA)的主要过敏原之一,CMA是一种具有广泛临床症状的疾病。本研究的目的是通过Pin-ELISA法评估BLG的连续B细胞表位。此外,我们想研究BLG致敏患者血清中IgE识别模式与接触牛奶后临床反应类型之间的可能关联。

方法

将与BLG氨基酸序列相对应的重叠连续十肽用于针对人IgE的Pin-ELISA。检测血清来自14名CMA患者,其中8名有速发型全身反应史,6名在接触牛奶后有迟发型皮肤反应。他们在CAP-RAST中均显示出针对BLG的特异性IgE抗体。对照血清来自5名健康非过敏个体。

结果

所有BLG致敏个体的血清均显示IgE与BLG对应于氨基酸95-113的一个区域结合。此外,个体血清还与另外两个区域,即12-27和124-135发生反应。用一种可溶性合成肽抑制IgE与BLG的结合证实了主要表位。在以急性全身反应或迟发型皮肤反应为特征的两组CMA患者中,对BLG的B细胞表位识别模式未发现差异。

结论

使用IgE Pin-ELISA,我们能够证实先前描述的BLG连续B细胞表位。然而,主要牛奶过敏原之一的识别模式并不能预测临床反应类型。

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