Douglas G N, Rubin A S
Immunology. 1977 May;32(5):669-79.
In cultures of spleen cells from mice immunized with horse erythrocytes (HRBC) 7 days earlier, the simultaneous addition of sheep erythrocytes (SRBC) and the priming antigen on day 0 resulted in the suppression of the anti-SRBC plaque-forming cell (PFC) response by day 5 compared to the response of similar cultures that received only SRBC. The cell-free culture fluid from specifically-stimulated, HRBC-primed cells, but not normal cells, contained a factor that nonspecifically inhibited the anti-SRBC PFC response of cultures of normal spleen cells to which SRBC and diluted supernatant aliquots were added at the beginning of culture. Suppressor activity was not manifest unless active supernatants were added on day 0 of a 5-day culture period. Inhibition of the reference plaque response was not due to cytotoxicity of the active material, decreased immunogenicity of the SRBC, or switchover from IgM to IgG plaque formation. The soluble mediator was released slowly into the culture fluid, with linear kinetics, from specifically activated, primed cells, with maximum suppression obtained with the 120-h supernatant. When active supernatants were fractionated by gel filtration over Sephadex G-150, the inhibitory factor eluted with molecules of about 34,000 mol. wt.
在7天前用马红细胞(HRBC)免疫的小鼠脾细胞培养物中,在第0天同时加入绵羊红细胞(SRBC)和致敏抗原,与仅接受SRBC的类似培养物的反应相比,到第5天时抗SRBC斑块形成细胞(PFC)反应受到抑制。来自特异性刺激的、经HRBC致敏的细胞而非正常细胞的无细胞培养液含有一种因子,该因子可非特异性抑制正常脾细胞培养物的抗SRBC PFC反应,在培养开始时向这些培养物中加入了SRBC和稀释的上清液等分试样。除非在5天培养期的第0天加入活性上清液,否则抑制活性不会显现。对参考斑块反应的抑制并非由于活性物质的细胞毒性、SRBC免疫原性降低或从IgM斑块形成转换为IgG斑块形成。可溶性介质从特异性激活的致敏细胞中以线性动力学缓慢释放到培养液中,120小时的上清液可获得最大抑制效果。当活性上清液通过Sephadex G - 150进行凝胶过滤分离时,抑制因子与分子量约为34,000的分子一起洗脱。