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对携带嵌合人-鼠I类主要组织相容性复合体的转基因小鼠中HLA限制的流感特异性细胞毒性T淋巴细胞反应的分析。

Analysis of the HLA-restricted influenza-specific cytotoxic T lymphocyte response in transgenic mice carrying a chimeric human-mouse class I major histocompatibility complex.

作者信息

Vitiello A, Marchesini D, Furze J, Sherman L A, Chesnut R W

机构信息

Department of Cellular Immunology, Cytel Corporation, La Jolla, California 92037.

出版信息

J Exp Med. 1991 Apr 1;173(4):1007-15. doi: 10.1084/jem.173.4.1007.

Abstract

Transgenic murine lines have been constructed that express a chimeric class I molecule composed of the alpha 1 and alpha 2 domains of HLA-A2.1 and the alpha 3, transmembrane, and cytoplasmic domains of H-2Kb. Upon immunization with influenza virus, transgenic mice developed a strong A2.1Kb-restricted cytotoxic T lymphocyte (CTL) response specific for the same matrix protein epitope that serves as the dominant A2.1-restricted determinant in the equivalent human response. Fine specificity analysis of CTL clones using truncated peptides revealed strong similarity between the response repertoire of transgenic mice and that previously reported using influenza-specific A2.1-restricted CTL clones from humans. This suggests that even when considering T cell responses by different species, the alpha 1 and alpha 2 domains of the restriction element play a dominant role in determining the CTL specific repertoire. Thus, substituting the alpha 3 domain of A2.1 with a murine counterpart has permitted development of a transgenic strain that should serve as an excellent model system in studies of HLA-restricted responses.

摘要

已构建出转基因鼠系,其表达一种嵌合的I类分子,该分子由HLA - A2.1的α1和α2结构域以及H - 2Kb的α3、跨膜和胞质结构域组成。用流感病毒免疫后,转基因小鼠产生了强烈的A2.1Kb限制性细胞毒性T淋巴细胞(CTL)反应,该反应针对与在相应人类反应中作为主要A2.1限制性决定簇的相同基质蛋白表位具有特异性。使用截短肽对CTL克隆进行精细特异性分析发现,转基因小鼠的反应库与先前报道的使用来自人类的流感特异性A2.1限制性CTL克隆的反应库之间具有很强的相似性。这表明,即使考虑不同物种的T细胞反应,限制元件的α1和α2结构域在决定CTL特异性反应库方面也起着主导作用。因此,用鼠类对应物替代A2.1的α3结构域已使得能够开发出一种转基因品系,该品系应可作为研究HLA限制性反应的优良模型系统。

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