Kayes S G, Colley D G
Cell Immunol. 1984 Jan;83(1):152-60. doi: 10.1016/0008-8749(84)90234-x.
Spleen cells from mice harboring infections of Schistosoma mansoni for 20 weeks exposed to Con A or to soluble schistosome egg antigenic preparation (SEA), treated with Mitomycin C (Mc), and cocultured with spleen cells from either normal or infected mice caused an augmented baseline [3H]TdR incorporation by the otherwise unstimulated responder cells. This regulation required an in vitro induction phase. SEA-exposed, Mc-treated normal spleen cells had no effect on responder cell cultures. SEA-stimulated, Mc-treated chronic spleen cell augmentation was effective on responder cell populations from either normal mice or mice infected with S. mansoni for 8 weeks. Augmentation was most pronounced when assayed on cells from infected mice assayed over a 5-day incubation. In addition, it is demonstrated that these Con A- and SEA-elicited activities are mediated by soluble mediators which lack H-2 restriction.
来自感染曼氏血吸虫20周的小鼠的脾细胞,暴露于刀豆蛋白A(Con A)或可溶性血吸虫卵抗原制剂(SEA),用丝裂霉素C(Mc)处理,并与来自正常或感染小鼠的脾细胞共培养,导致原本未受刺激的反应细胞的基线[3H]胸苷掺入增加。这种调节需要一个体外诱导阶段。暴露于SEA、经Mc处理的正常脾细胞对反应细胞培养物没有影响。经SEA刺激、Mc处理的慢性脾细胞增殖对来自正常小鼠或感染曼氏血吸虫8周的小鼠的反应细胞群体有效。在对感染小鼠的细胞进行5天培养后进行检测时,增殖最为明显。此外,还证明这些由Con A和SEA引发的活性是由缺乏H-2限制的可溶性介质介导的。