Eardley D D, Gershon R K
J Immunol. 1976 Jul;117(1):313-8.
We describe conditions for generating sheep red blood cell-specific suppressor T cells in Mishell-Dutton cultures. The production of specific suppressor cells is favored by increasing antigen dose in the initial culture but can be produced by transferring more cells when lower doses of antigen are used. Transfer of small numbers of cells cultured with low doses of antigen leads to a specific helper effect. Transfer of large numbers of educated cells leads to nonspecific suppression. Suppression can be effected by the effluent cells from nylon wool columns which do not make detectable PFC. A fraction of these cells become resistant to treatment with anti-T cell sera and complement after culture. The suppressor cells are radiation sensitive and must be able to synthesize protein to suppress. They take 2 to 3 days of education to reach maximum suppressive efficiency and will not suppress cultures if added 2 to 3 days after culture initiation. Their production is favored by the absence of mercaptoethanol, suggesting that the observed suppression is not "too much help". The ability to generate specific suppressor cells in vitro should be of great benefit in determining the factors that regulate their appearance in vivo.
我们描述了在米舍尔-达顿培养体系中产生绵羊红细胞特异性抑制性T细胞的条件。在初始培养中增加抗原剂量有利于特异性抑制细胞的产生,但当使用较低剂量抗原时,通过转移更多细胞也可产生。用低剂量抗原培养后转移少量细胞会产生特异性辅助效应。转移大量受过刺激的细胞会导致非特异性抑制。用尼龙毛柱流出的细胞(这些细胞不能产生可检测到的空斑形成细胞)可实现抑制。这些细胞中的一部分在培养后对抗T细胞血清和补体处理产生抗性。抑制性细胞对辐射敏感,且必须能够合成蛋白质才能发挥抑制作用。它们需要2至3天的“训练”才能达到最大抑制效率,并且如果在培养开始后2至3天才添加,则不会抑制培养物。巯基乙醇的缺失有利于它们的产生,这表明观察到的抑制并非“过度辅助”。体外产生特异性抑制细胞的能力对于确定调节其在体内出现的因素应具有极大的益处。