对蚊子过敏原的免疫反应与交叉反应性蜂毒成分有关:交叉反应性碳水化合物决定因素(CCDs)在蜜蜂-蚊子综合征中的重要性

IF 2.6 Q2 ALLERGY
C G Uasuf, C D'Anna, C Di Sano, V Blanda, E Scala, M Barrale, I Brusca, A Torina
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引用次数: 0

摘要

摘要:背景。蚊子是双翅目的一个科。在世界各地,有两种能够吸人血并传播疾病的类群:按蚊和库蚊,包括库蚊、伊蚊和社区伊蚊(Ac)等几个属。先前的研究表明,Ac致敏与提取物或单一蜂毒成分之间存在显著关系,表明存在“蜂蚊综合征”。本研究的目的是鉴定蚊子和蜂毒提取物与IgE阳性血清之间的交叉反应带。方法。对21例不同类型的蚊虫和蜜蜂过敏个体进行血清与室内蚊虫和蜜蜂提取物的联合检测。使用/不使用CCD抑制剂进行SDS-PAGE和(IB)检测。结果。不含CCD抑制剂的数据表明,雄库蚊、雌库蚊和伊蚊之间的IgE结合条带约为~21kDa、~35kDa、~40kDa和~55kDa。虽然从蜜蜂提取物中观察到IgE结合的蛋白质带,但这些带与蚊子提取物中存在的任何条带不一致。CCD抑制剂的数据导致IgE结合的差异。先前在40和90 kDa的蜜蜂毒液样品中观察到的条带消失了。虽然印迹看起来更干净,但在蚊子样本的条带模式上没有观察到重大差异。结论。IB数据表明,CCD抑制剂的使用可阻止蚊虫过敏患者的IgE与蜜蜂毒液的多个条带结合。可以推断,最初出现在40kDa和90kda的波段可能是由于CCD相互作用。在15-20 kDa之间仍存在两条条带,但与蚊子提取物中存在的任何条带不一致。进一步的实验必须确定来自蜜蜂的反应带是不相关的蛋白质还是不同分子量的相关同源蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune response to mosquito allergens is associated with cross-reactive bee venom components: the importance of cross-reactive carbohydrate determinants (CCDs) in the Bee-Mosquito Syndrome.

Summary: Background. Mosquitoes are a family of the order Diptera. Throughout the world, there are two groups able to suck human blood and transmit diseases: the anophelines and the culicines comprise several genera such as Culex, Aedes and Aedes communis (Ac). Previous study has demostrated a significant relationship between Ac sensitization and either extract or single bee venom components suggesting a "bee-mosquito syndrome" occurrence. The aim of the study was to identify bands of cross reactivity between the extracts of Mosquito and Bee venom, with IgE positive sera. Methods. Serum from 21 different Mosquito and A. mellifera allergic individuals were combined with extracts of Mosquito (in house) and A. mellifera. SDS-PAGE and (IB) were carried out with/without CCD inhibitor. Results. The data without CCD inhibitor suggests IgE binding to common bands between Culex male, Culex female and Aedes of approx ~21kDa, ~35kDa, ~40kDa and ~55kDa. Whilst IgE binding has been observed to protein bands from the A. mellifera extract, these bands do not align with any present in the mosquito extracts. Data with CCD inhibitor results in differences in IgE binding. Bands that were previously observed in the A. mellifera venom sample at 40 and 90 kDa, disappeared. No major differences in banding pattern were observed for the mosquito samples, although the blot appears cleaner. Conclusions. IB data suggests that the use of CCD inhibitor prevents binding of IgE from mosquito allergic patients to multiple bands from A. mellifera venom. It may be inferred that bands originally present at 40kDa and 90 kDa may have been due to a CCD interaction. Two bands remain present in the A. mellifera sample between 15-20 kDa, however do not align with any bands present in the mosquito extracts. Further experiments must be done to determine whether the reactive bands from A. mellifera are unrelated proteins or whether the proteins are related homologues of varying MW.

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