人t细胞过敏原表位的定位。

Thomas Zeiler, Tuomas Virtanen
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引用次数: 5

摘要

过敏原的特点是能够与转基因结合。Swiss-Prot蛋白质数据库目前列出了超过350种过敏原的部分或完整氨基酸序列。目前尚不清楚过敏原如何参与过敏致敏过程,即特异性t辅助2型(Th2)淋巴细胞的产生,而Th2淋巴细胞在刺激B淋巴细胞产生过敏原特异性IgE中起着至关重要的作用。辅助性t细胞(Th)在调节免疫应答中起着关键作用。T细胞对抗原的识别是复杂的,它可以触发定性差异信号。因此,可以想象,Th细胞识别的表位或抗原决定因子可能会影响免疫反应的质量。本章的目的是描述t细胞表位可以被识别(映射)的方式。这一点尤其重要,因为了解过敏原的精确t细胞表位可以提供有关过敏发病机制的重要信息,并有助于为过敏的诊断和/或免疫治疗提供更好的准备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping of human T-cell epitopes of allergens.

Allergens are characterized by their ability to be bound by gE. The Swiss-Prot protein database currently lists a partial or complete amino acid sequence of in excess of about 350 allergens. It is not clear how allergens participate in the process of allergic sensitization, the generation of specific T-helper type 2 (Th2) lymphocytes, which play a crucial role in stimulating B lymphocytes to produce allergen-specific IgE.T-helper (Th) cells play a key role in the regulation of immune responses. The recognition of antigen by T cells is complex and it can trigger qualitatively differential signaling. Therefore, it is conceivable that epitopes or antigenic determinants recognized by Th cells may influence the quality of immune response. The aim of this chapter is to describe the way in which T-cell epitopes can be identified (mapped). This is particularly important because knowledge of the precise T-cell epitopes of allergens can give important information on the pathogenesis of allergy and can help to develop better preparations for the diagnostics and/or immunotherapy of allergy.

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