Schiek W
Z Immunitatsforsch Exp Klin Immunol. 1975 May;148(5):431-50.
Peritoneal cells from normal, unimmunized mice (female NMRI, 28-32 gr) produced in vitro primary and secondary immune response after induction with the bacteriophage T2 6 hours or 7 day resp. after establishing the cultures. We confirmed the induction of a primary and secondary immunological response in vitro in the very same culture by the following data: 1. In vivo the donor animals were not in contact with the antigen used. We found neither the phage nor its host E. coli B in the gut of 97 mice investigated and no humoral antibodies against T2. The kinetics of humoral antibody production in vivo by different doses of T2 also showed that there are no related or identical antigen structures incorporated in our animals. 2. The T2 neutralizing activity in the culture medium after the first induction had the sedimentation constant of 19.7 +/- 2.3 S (n = 9) but the activity found after the second induction sedimented with 8.1 +/- 0.7 S (n = 10). 3. The primary activity was more sensitive to mercaptoethanol than the secondary. 4. Complement was bound by the complex T2 + neutralizing activity.
来自正常、未免疫小鼠(雌性NMRI,体重28 - 32克)的腹膜细胞,在分别于培养建立后6小时或7天用噬菌体T2诱导后,在体外产生了初次和二次免疫反应。我们通过以下数据证实了在同一培养物中体外诱导出了初次和二次免疫反应:1. 在体内,供体动物未接触所用抗原。在对97只小鼠进行检查时,我们在其肠道中既未发现噬菌体,也未发现其宿主大肠杆菌B,且未发现针对T2的体液抗体。不同剂量的T2在体内产生体液抗体的动力学也表明,我们的动物体内不存在相关或相同的抗原结构。2. 初次诱导后培养基中的T2中和活性沉降常数为19.7 +/- 2.3 S(n = 9),但二次诱导后发现的活性沉降常数为8.1 +/- 0.7 S(n = 10)。3. 初次活性比二次活性对巯基乙醇更敏感。4. 补体与T2 + 中和活性复合物结合。