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通过合成肽对HIV蛋白上的IgG亚类和T细胞表位进行图谱分析。

Mapping of IgG subclass and T-cell epitopes on HIV proteins by synthetic peptides.

作者信息

Mathiesen T, Broliden P A, Rosen J, Wahren B

机构信息

National Bacteriological Laboratory, Karolinska Institute, Stockholm, Sweden.

出版信息

Immunology. 1989 Aug;67(4):453-9.

Abstract

Fifteen amino acid peptides, sequentially overlapping by 10 amino acids, were synthesized on the basis of the HTLV-III sequences of the gag and env proteins. They were used as antigens in IgG subclass ELISAs and T-cell stimulation assays. Sera and cells were obtained from 30 asymptomatic, HIV-infected homosexuals. In all subclasses reactivity was found to parts of the gag protein, while IgG1 dominated anti-env peptide responses. It was possible to delineate peptides showing restricted IgG subclass responses that were dominated by either IgG1, 2, 3 or 4. A negative correlation was generally observed between B-cell and T-cell reactivity, but a T-cell and B-cell co-operation was suggested by the response to two IgG1-restricted peptides. The IgG3-dominated epitopes were present in peptides previously known to be amphipathic and capable of T-cell stimulation. The analysis of subclass-restricted responses on the peptide level will assist the understanding of the subclass expression in vivo, since the peptide mapping approximates the delineation of a subclass-restricted response at the level of single epitopes.

摘要

基于人类嗜T淋巴细胞病毒III型(HTLV - III)gag和env蛋白的序列,合成了15个氨基酸的肽段,这些肽段依次重叠10个氨基酸。它们被用作IgG亚类酶联免疫吸附测定(ELISA)和T细胞刺激试验中的抗原。血清和细胞取自30名无症状的、感染了HIV的同性恋者。在所有亚类中,均发现针对gag蛋白部分的反应性,而IgG1在抗env肽反应中占主导。有可能描绘出显示出受限制的IgG亚类反应的肽段,这些反应分别由IgG1、2、3或4主导。一般观察到B细胞和T细胞反应性之间呈负相关,但对两种受IgG1限制的肽段的反应提示了T细胞和B细胞之间的合作。以IgG3为主的表位存在于先前已知具有两亲性且能够刺激T细胞的肽段中。在肽段水平上对亚类限制反应的分析将有助于理解体内亚类的表达,因为肽图谱绘制在单个表位水平上近似于对亚类限制反应的描绘。

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