Lefkovits I, QUintáns J, Munro A, Waldmann H
Immunology. 1975 Jun;28(6):1149-54.
Supernatants were collected from keyhole limpet haemocyanin (KLH) primed spleen cells which had been incubated in tissue culture medium with their priming antigen KLH. These non-specific factor (NSF) containing supernatants were then tested in a microculture system for their ability to facilitate an anti-SRBC response of nu/nu or AT times BM spleen cells. It was concluded that:(a) NSF was able to engage a large number of the available pool of sheep erythrocyte (SRBC) specific B cells into an antibody response (b) this response was characterized by the development of clones expressing plaque-forming cells (PFC), the number of PFC produced within a clone being dependent upon the amount of NSF available in that culture; (c) NSF probably acted directly on B cells, and not via other accessory cell types.
从预先用钥孔戚血蓝蛋白(KLH)致敏的脾细胞中收集上清液,这些脾细胞已在组织培养基中与它们的致敏抗原KLH一起孵育。然后在微量培养系统中测试这些含有非特异性因子(NSF)的上清液促进无胸腺裸鼠(nu/nu)或经照射的骨髓脾细胞抗绵羊红细胞(SRBC)反应的能力。得出以下结论:(a)NSF能够使大量可用的绵羊红细胞(SRBC)特异性B细胞库参与抗体反应;(b)这种反应的特征是表达空斑形成细胞(PFC)的克隆的发展,克隆内产生的PFC数量取决于该培养物中可用的NSF量;(c)NSF可能直接作用于B细胞,而不是通过其他辅助细胞类型。