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在HIV-1 NEF蛋白中心区域与人类细胞毒性CD8 + T细胞发生反应的六个表位。

Six epitopes reacting with human cytotoxic CD8+ T cells in the central region of the HIV-1 NEF protein.

作者信息

Culmann B, Gomard E, Kiény M P, Guy B, Dreyfus F, Saimot A G, Sereni D, Sicard D, Lévy J P

机构信息

Institut Cochin de Génétique Moléculaire, Institut de la Santé et de la Recherche Medicale 152-Centre National de la Recherche Scientifique 628, Hôpital Cochin, Paris, France.

出版信息

J Immunol. 1991 Mar 1;146(5):1560-5.

PMID:1704397
Abstract

In order to identify the target epitopes recognized by specific CTL in the NEF protein of HIV-1, 33 peptides derived from the HIV-BRU sequence were tested with NEF-specific CTL generated from HIV-seropositive donors. Six different epitopes were identified and several points were remarkable: 1) They were all located in two regions of the central part of the NEF protein corresponding to residues 73 to 94 and 113 to 147, respectively. 2) The CTL issued from a single donor could recognize several peptides of the NEF protein. 3) Some of these peptides could be recognized in association with at least two or three different HLA class I molecules. 4) Two different overlapping epitopes were present in a relatively short sequence of 15 amino acids. These results suggest that multiple epitopes corresponding to different HLA restrictions could coexist in a relatively small region of the NEF protein. The implications of these results in vaccine strategies using synthetic peptides bearing CTL epitopes are discussed.

摘要

为了鉴定HIV-1的NEF蛋白中被特异性CTL识别的靶表位,用来自HIV血清阳性供体产生的NEF特异性CTL检测了源自HIV-BRU序列的33个肽段。鉴定出6个不同的表位,有几点值得注意:1)它们都位于NEF蛋白中央部分的两个区域,分别对应于第73至94位氨基酸残基和第113至147位氨基酸残基。2)来自单个供体的CTL可以识别NEF蛋白的几种肽段。3)其中一些肽段可以与至少两到三种不同的HLA I类分子结合被识别。4)在15个氨基酸的相对短序列中存在两个不同的重叠表位。这些结果表明,对应于不同HLA限制的多个表位可能共存于NEF蛋白的一个相对小的区域。讨论了这些结果在使用带有CTL表位的合成肽的疫苗策略中的意义。

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