Cihak J, Lehmann-Grube F
Immunology. 1978 Feb;34(2):265-75.
Previous studies have shown that no cell-mediated immunity against LCM virus-infected cells can be detected in neonatally established LCM virus carrier mice suggesting that they are immunologically tolerant to virally-altered cell membrane antigens. In this communication experiments are described aimed at analyzing the mechanism. Virus-specific cell-mediated immunity was assessed by 51Cr release and target cell reduction assays. Attempts to demonstrate cells in spleens of CBA/J carrier mice able to suppress in syngeneic recipients the induction or the effector phase of the cytotoxic T-cell response against LCM virus-infected cells were unsuccessful. Also, no factors were detected in CBA/J and C57BL/6J carrier mice, either spleen cell-associated or free in the circulation, which would block the activity of cytotoxic T-lymphocytes against LCM virus-infected syngeneic target cells. The results indicate that inability of LCM virus carrier mice to act immunologically against virus-infected target cells is due to deletion or irreversible inactivation of T lymphocytes carrying receptors for virally altered cell membrane antigens.
先前的研究表明,在新生期建立的淋巴细胞性脉络丛脑膜炎病毒(LCM病毒)携带小鼠中,检测不到针对LCM病毒感染细胞的细胞介导免疫,这表明它们对病毒改变的细胞膜抗原具有免疫耐受性。在本通讯中,描述了旨在分析该机制的实验。通过51Cr释放和靶细胞减少试验评估病毒特异性细胞介导免疫。试图在CBA/J携带小鼠的脾脏中证明能够在同基因受体中抑制针对LCM病毒感染细胞的细胞毒性T细胞反应的诱导或效应阶段的细胞,但未成功。此外,在CBA/J和C57BL/6J携带小鼠中,无论是与脾细胞相关的还是循环中游离的,均未检测到会阻断细胞毒性T淋巴细胞对LCM病毒感染的同基因靶细胞活性的因子。结果表明,LCM病毒携带小鼠无法对病毒感染的靶细胞产生免疫作用,是由于携带病毒改变的细胞膜抗原受体的T淋巴细胞缺失或不可逆失活所致。