Kontiainen S, Woody J N, Rees A, Feldmann M
Clin Exp Immunol. 1981 Mar;43(3):517-25.
Based on methods used for the in vitro induction of antigen-specific suppressor cells in the mouse, we have cultured Ficoll-Isopaque-separated human blood cells with high dose of antigen (100 microgram/ml) in Marbrook culture vessels for 4 days. The resulting cells, when further recultured for 24 hr with a low dose of antigen (1 microgram/ml), released into the supernatant material, termed 'suppressor factor', which inhibited, in an antigen-specific manner, the antibody response of mouse spleen cells in culture. The suppressor factor was analysed using immunoabsorbents, and was bound to and eluted from specific antigen, concanavalin A and lentil lectin, anti-human Ia antibodies, and anti-mouse suppressor factor antibodies, but was not bound to antibodies against human IgG.
基于用于在小鼠体内体外诱导抗原特异性抑制细胞的方法,我们将经Ficoll-Isopaque分离的人血细胞与高剂量抗原(100微克/毫升)在Marbrook培养容器中培养4天。所得细胞在与低剂量抗原(1微克/毫升)进一步再培养24小时后,释放出一种称为“抑制因子”的物质到上清液中,该抑制因子以抗原特异性方式抑制培养的小鼠脾细胞的抗体反应。使用免疫吸附剂对抑制因子进行分析,发现它能与特异性抗原、伴刀豆球蛋白A和扁豆凝集素、抗人Ia抗体以及抗小鼠抑制因子抗体结合并从其上洗脱,但不与抗人IgG抗体结合。