Heeg K, Wagner H
Eur J Immunol. 1985 Jan;15(1):25-30. doi: 10.1002/eji.1830150106.
Injection of (CBA X A)F1 cells into neonatal CBA mice rendered them tolerant to skin grafts of (CBA X A)F1 origin. Limiting dilution analysis revealed a very low frequency of tolerogen-inducible cytotoxic T lymphocyte precursors (CTL-P) in spleens of tolerant mice. Two in vitro procedures allowed, however, the induction of tolerogen-specific CTL-P of high frequencies in tolerant mice: (a) the "by-pass" activation of spleen cells from tolerant mice by concanavalin A under short-term bulk culture conditions followed by culture of limiting numbers of activated responder cells, and (b) absorption of spleen cells from tolerant mice on monolayers of tolerogen-activated T cells from normal syngeneic mice. Furthermore, spleen cells from tolerant mice, recently challenged with a tolerogen-bearing skin graft, specifically suppressed the activation of tolerogen-reactive splenic CTL-P from normal CBA mice under limiting dilution conditions. These data confirm the presence of tolerogen-specific CTL-P of high frequency in tolerant mice and suggest their functional inactivation through a suppressive mechanism.
将(CBA×A)F1细胞注射到新生CBA小鼠体内,可使其对(CBA×A)F1来源的皮肤移植物产生耐受。有限稀释分析显示,耐受小鼠脾脏中可诱导耐受原的细胞毒性T淋巴细胞前体(CTL-P)频率极低。然而,两种体外方法可在耐受小鼠中诱导出高频率的耐受原特异性CTL-P:(a)在短期大量培养条件下,用刀豆球蛋白A对耐受小鼠的脾细胞进行“旁路”激活,随后培养有限数量的活化反应细胞;(b)将耐受小鼠的脾细胞吸附在正常同基因小鼠的耐受原激活T细胞单层上。此外,最近用携带耐受原的皮肤移植物攻击过的耐受小鼠的脾细胞,在有限稀释条件下可特异性抑制正常CBA小鼠中耐受原反应性脾CTL-P的激活。这些数据证实了耐受小鼠中存在高频率的耐受原特异性CTL-P,并提示它们通过抑制机制发生功能失活。