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鉴定人类免疫缺陷病毒1型Nef蛋白中被细胞毒性T淋巴细胞识别的多限制性免疫显性区域。

Identification of multirestricted immunodominant regions recognized by cytolytic T lymphocytes in the human immunodeficiency virus type 1 Nef protein.

作者信息

Culmann-Penciolelli B, Lamhamedi-Cherradi S, Couillin I, Guegan N, Levy J P, Guillet J G, Gomard E

机构信息

Laboratoire d'Immunologie des Interactions Cellulaires et Moléculaires, Institut National de la Santé et de la Recherche Médicale U152. Institut Cochin de Génétique Moléculaire, Paris, France.

出版信息

J Virol. 1994 Nov;68(11):7336-43. doi: 10.1128/JVI.68.11.7336-7343.1994.

Abstract

Peripheral blood mononuclear cells from a large number of human immunodeficiency virus (HIV)-seropositive donors were used to analyze the CD8+ T-cell response to each part of the Nef protein of HIV-1/LAI. This report identifies an immunodominant region (amino acids 73 to 144) in the Nef protein that was recognized by 97% of the NEF responder donors. This peptide sequence was dissected into four epitopic regions (amino acids 73 to 82, 83 to 97, 113 to 128, and 126 to 144), each of which was recognized under different HLA class I restrictions. Short overlapping peptides were used to sensitive the target cells for cytolysis and so to determine if these epitopic regions were multirestricted. Each region was found to contain several epitopes recognized with different HLA molecules. Thus, the central region of the Nef protein, a regulatory protein expressed early in HIV-infected cells, is rich in epitopic sequences which are found to be similar in many infected individuals and which can be recognized in association with at least ten HLA class I molecules. Their implications for the vaccination of humans with peptide sequences are discussed.

摘要

来自大量人类免疫缺陷病毒(HIV)血清反应阳性供体的外周血单个核细胞被用于分析CD8 + T细胞对HIV-1/LAI的Nef蛋白各部分的反应。本报告鉴定出Nef蛋白中的一个免疫显性区域(氨基酸73至144),97%的Nef反应性供体可识别该区域。该肽序列被分解为四个表位区域(氨基酸73至82、83至97、113至128和126至144),每个区域在不同的HLA I类限制下被识别。使用短重叠肽使靶细胞对细胞溶解敏感,从而确定这些表位区域是否受到多种限制。发现每个区域都包含几个可被不同HLA分子识别的表位。因此,Nef蛋白的中央区域,一种在HIV感染细胞早期表达的调节蛋白,富含表位序列,这些序列在许多感染个体中相似,并且可以与至少十种HLA I类分子结合被识别。讨论了它们对用肽序列对人类进行疫苗接种的意义。

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