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变应原性的分子基础。

The molecular basis of allergenicity.

作者信息

Shakib Farouk, Ghaemmaghami Amir M, Sewell Herb F

机构信息

Division of Immunology, School of Molecular Medical Sciences, Institute of Infection, Immunity and Inflammation, University of Nottingham, Queen's Medical Centre, Nottingham, UK.

出版信息

Trends Immunol. 2008 Dec;29(12):633-42. doi: 10.1016/j.it.2008.08.007. Epub 2008 Oct 24.

Abstract

Allergens are mostly innocuous antigens that elicit powerful T helper cell type 2 (Th2) responses leading to hyper-immunoglobulin E (IgE) production and allergy. Research carried out over several years has highlighted the possible role of the inherent protease activity, surface features and glycosylation patterns of allergens in the engagement of a Th2 signalling pathway. It is thought that allergens possess common features and patterns that enable them to be recognized by innate immune defences as Th2-inducing antigens. These events are further amplified by proteolytically active allergens through digestion of cell surface molecules involved in regulating innate and adaptive immune functions, favouring Th2 responses. A greater understanding of the molecular features that make proteins allergenic will help define new therapeutic targets aimed at blocking allergen recognition and protease activity.

摘要

变应原大多是无害抗原,可引发强大的2型辅助性T细胞(Th2)反应,导致免疫球蛋白E(IgE)过度产生和过敏。多年来开展的研究突出了变应原固有的蛋白酶活性、表面特征和糖基化模式在Th2信号通路激活过程中的可能作用。据认为,变应原具有共同特征和模式,使其能够被固有免疫防御识别为诱导Th2的抗原。这些事件会被具有蛋白水解活性的变应原通过消化参与调节固有免疫和适应性免疫功能的细胞表面分子而进一步放大,从而有利于Th2反应。更深入了解使蛋白质具有变应原性的分子特征将有助于确定旨在阻断变应原识别和蛋白酶活性的新治疗靶点。

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