Klein J R, Pasternack M S, Bevan M J
J Immunol. 1985 Apr;134(4):2456-61.
We have studied the activation signals that regulate interferon-gamma (IFN-gamma) secretion from murine cytotoxic T lymphocytes (CTL) upon binding mitogen or antigen. CTL clones were found to require at least 1 hr of stimulation with concanavalin A (Con A) in order to produce detectable levels of IFN-gamma. Full activation of IFN-gamma synthesis in CTL clones occurred after stimulation for 2 hr or more, and in those cultures CTL continued to produce high levels of IFN-gamma even after the effects of Con A had been neutralized. Splenic T cells and uncloned long-term CTL lines required a longer period of stimulation than cloned CTL for Con A-induced IFN-gamma secretion. The relationship between IFN-gamma secretion and cytotoxic activity was studied in an antigen-specific system. These studies reveal marked differences in the types of effector responses generated by CTL upon contact with antigen, demonstrating that some antigen-bearing cells promote high levels of IFN-gamma secretion and are poorly lysed by CTL, whereas other cell lines are lysed with high efficiency by CTL but induce low levels of IFN-gamma secretion.
我们研究了在结合丝裂原或抗原后,调节小鼠细胞毒性T淋巴细胞(CTL)分泌干扰素-γ(IFN-γ)的激活信号。发现CTL克隆需要用伴刀豆球蛋白A(Con A)刺激至少1小时才能产生可检测水平的IFN-γ。CTL克隆中IFN-γ合成的完全激活在刺激2小时或更长时间后发生,并且在那些培养物中,即使Con A的作用已被中和,CTL仍继续产生高水平的IFN-γ。对于Con A诱导的IFN-γ分泌,脾T细胞和未克隆的长期CTL系比克隆的CTL需要更长的刺激时间。在抗原特异性系统中研究了IFN-γ分泌与细胞毒性活性之间的关系。这些研究揭示了CTL与抗原接触后产生的效应反应类型存在显著差异,表明一些携带抗原的细胞促进高水平的IFN-γ分泌,且被CTL裂解的效率较低,而其他细胞系被CTL高效裂解,但诱导的IFN-γ分泌水平较低。