Fox R A, Rajaraman K
Immunol Commun. 1978;7(3):311-21. doi: 10.3109/08820137809025475.
The production of migration inhibition factor (MIF) by human peripheral blood lymphocytes and guinea pig lymph node lymphocytes, in response to mitogen, concanavalin A, or antigen, tuberculin, has been studied. Suppressor cells have been depleted by in vitro ageing of cultures for 24 hours, and this has resulted in a significant increase in MIF activity. Reconstitution of the aged lymphocyte population by the addition of fresh lymphocytes results in a suppression of MIF production. When lymphocytes, which have been cultured for 24 hours in the presence of antigen or mitogen to generate suppressor cells, are added to aged cultures MIF production is inhibited. These results suggest that suppressor cells play a regulatory role in the production of MIF.
已对人外周血淋巴细胞和豚鼠淋巴结淋巴细胞在有丝分裂原刀豆球蛋白A 或抗原结核菌素刺激下产生迁移抑制因子(MIF)的情况进行了研究。通过体外培养24小时使培养物老化来去除抑制细胞,这导致MIF活性显著增加。添加新鲜淋巴细胞对老化淋巴细胞群体进行重建,会抑制MIF的产生。当在抗原或有丝分裂原存在的情况下培养24小时以产生抑制细胞的淋巴细胞添加到老化培养物中时,MIF的产生受到抑制。这些结果表明,抑制细胞在MIF的产生中起调节作用。