Caton A J, Stark S E, Shih F F, Cerasoli D M
Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
J Clin Immunol. 1995 Nov;15(6 Suppl):106S-112S. doi: 10.1007/BF01540900.
We have generated transgenic mouse lineages that express the influenza virus hemagglutinin in different physical forms. One kind expresses the full-length hemagglutinin molecule as a cell surface glycoprotein and can be recognized by hemagglutinin-specific B and T cells. The other expresses a truncated polypeptide corresponding to the N-terminal third of the hemagglutinin molecule. This polypeptide encodes known hemagglutinin-specific T-cell determinants; however, it contains no native B-cell epitopes, since these depend on the conformation of the fully folded protein. In each case, the hemagglutinin transgenic mice display ubiquitous expression of transgenic messenger RNA and induce T-cell tolerance to the transgene-encoded T-cell determinant site 1. Thus, the hemagglutinin is a neo-self-antigen in both kinds of hemagglutinin transgenic mice and should provide a useful system for understanding the factors and mechanisms that govern tolerance and autoimmunity to self-antigens.
我们已经培育出了以不同物理形式表达流感病毒血凝素的转基因小鼠品系。一种品系将全长血凝素分子表达为细胞表面糖蛋白,可被血凝素特异性B细胞和T细胞识别。另一种品系表达对应于血凝素分子N端三分之一的截短多肽。这种多肽编码已知的血凝素特异性T细胞决定簇;然而,它不包含天然B细胞表位,因为这些表位依赖于完全折叠蛋白的构象。在每种情况下,血凝素转基因小鼠均表现出转基因信使RNA的普遍表达,并诱导对转基因编码的T细胞决定簇位点1的T细胞耐受。因此,在这两种血凝素转基因小鼠中,血凝素都是一种新的自身抗原,应该为理解控制对自身抗原的耐受和自身免疫的因素及机制提供一个有用的系统。