Sharpe A H, Gaulton G N, Ertl H C, Finberg R W, McDade K K, Fields B N, Greene M I
J Immunol. 1985 Apr;134(4):2702-6.
Cytotoxic T lymphocyte (Tc) cell lines specific for reovirus type 3 lysed an uninfected B cell hybridoma line, 87.92.6, that expresses and secretes an anti-idiotypic antibody that reacts with an anti-viral hemagglutinin monoclonal antibody, 9BG5. Monoclonal anti-idiotype 87.92.6 was shown by fluorescence analysis to specifically bind to reovirus Tc and to block reovirus-specific Tc from killing reovirus-infected target cells or the 87.92.6 hybridoma. An anti-LFA-1 monoclonal antibody, M17, interfered with Tc-mediated lysis of reovirus-infected targets and the 87.92.6 cells, indicating the similarity of cellular interactions mediated by LFA-1 structures when Tc bind to virally infected targets or 87.92.6 targets. Together with studies in which anti-H2 or monoclonal idiotypic antibodies were found to interfere with reovirus-specific Tc recognition of virally infected or 87.92.6 targets, these experiments indicate that some reovirus-specific Tc have conformations in their receptor that can be recognized by anti-idiotype.
对3型呼肠孤病毒具有特异性的细胞毒性T淋巴细胞(Tc)细胞系可裂解未感染的B细胞杂交瘤细胞系87.92.6,该细胞系表达并分泌一种抗独特型抗体,该抗体可与抗病毒血凝素单克隆抗体9BG5发生反应。荧光分析显示,单克隆抗独特型87.92.6可特异性结合呼肠孤病毒Tc,并阻止呼肠孤病毒特异性Tc杀伤呼肠孤病毒感染的靶细胞或87.92.6杂交瘤细胞。抗LFA-1单克隆抗体M17可干扰Tc介导的对呼肠孤病毒感染靶细胞和87.92.6细胞的裂解,这表明当Tc与病毒感染的靶细胞或87.92.6靶细胞结合时,由LFA-1结构介导的细胞相互作用具有相似性。与抗H2或单克隆独特型抗体干扰呼肠孤病毒特异性Tc对病毒感染或87.92.6靶细胞的识别的研究一起,这些实验表明,一些呼肠孤病毒特异性Tc的受体具有可被抗独特型识别的构象。