Sevilla N, Homann D, von Herrath M, Rodriguez F, Harkins S, Whitton J L, Oldstone M B
Division of Virology, Department of Neuropharmacology, The Scripps Research Institute, La Jolla, California 92037, USA.
J Virol. 2000 Apr;74(7):3284-92. doi: 10.1128/jvi.74.7.3284-3292.2000.
Virus-specific cytotoxic T lymphocytes (CTL) at frequencies of >1/1, 000 are sufficient to cause insulin-dependent diabetes mellitus (IDDM) in transgenic mice whose pancreatic beta cells express as "self" antigen a protein from a virus later used to initiate infection. The inability to generate sufficient effector CTL for other cross-reacting viruses that fail to cause IDDM could be mapped to point mutations in the CTL epitope or its COO(-) flanking region. These data indicate that IDDM and likely other autoimmune diseases are caused by a quantifiable number of T cells, that neither standard epidemiologic markers nor molecular analysis with nucleic acid probes reliably distinguishes between viruses that do or do not cause diabetes, and that a single-amino-acid change flanking a CTL epitope can interfere with antigen presentation and development of autoimmune disease in vivo.
频率大于1/1000的病毒特异性细胞毒性T淋巴细胞(CTL)足以在转基因小鼠中引发胰岛素依赖型糖尿病(IDDM),这些转基因小鼠的胰腺β细胞将一种后来用于引发感染的病毒蛋白作为“自身”抗原表达。对于其他未能引发IDDM的交叉反应病毒,无法产生足够的效应CTL可归因于CTL表位或其COOH(-)侧翼区域的点突变。这些数据表明,IDDM以及可能的其他自身免疫性疾病是由可量化数量的T细胞引起的,标准流行病学标志物和核酸探针分子分析都无法可靠地区分引发或不引发糖尿病的病毒,并且CTL表位侧翼的单个氨基酸变化可在体内干扰抗原呈递和自身免疫性疾病的发展。