Starzinski-Powitz A, Pfizenmaier K, Koszinowski U, Röllinghoff M, Wagner H
Eur J Immunol. 1976 Sep;6(9):630-4. doi: 10.1002/eji.1830060907.
Infection of H-2-identical mice with either lymphocytic choriomeningitis (LCM) virus, vaccinia virus, or paramyxo (Sendai) virus resulted in the generation of specifically sensitized cytotoxic T lymphocytes (CTL). CTL generated in vitro against 2,4,6-trinitrophenyl (TNP)-conjugated syngeneic stimulator cells were specifically cytotoxic for TNP-conjugated H-2K (D) region identical targets. Both LCM and vaccinia-induced CTL, however, were found to be strongly cytotoxic towards TNP-conjugated, H-2K(D) region-identical target cells. In contrast, Sendai virus-induced CTL did not lyse TNP-conjugated, syngeneic target cells. Inhibition experiments using cold targets suggested that shared antigenic determinants can be detected on either LCM virus-infected and TNP-conjugated targets, which are not present on the cell surface of normal target cells.
用淋巴细胞性脉络丛脑膜炎(LCM)病毒、痘苗病毒或副粘病毒(仙台病毒)感染H-2相同的小鼠,会导致产生特异性致敏的细胞毒性T淋巴细胞(CTL)。体外产生的针对2,4,6-三硝基苯基(TNP)偶联的同基因刺激细胞的CTL,对TNP偶联的H-2K(D)区域相同的靶细胞具有特异性细胞毒性。然而,发现LCM和痘苗诱导的CTL对TNP偶联的、H-2K(D)区域相同的靶细胞具有强烈的细胞毒性。相比之下,仙台病毒诱导的CTL不会裂解TNP偶联的同基因靶细胞。使用冷靶的抑制实验表明,在LCM病毒感染的和TNP偶联的靶细胞上可以检测到共同的抗原决定簇,而正常靶细胞的细胞表面不存在这些抗原决定簇。