Nelson R D, Leu R W
J Immunol. 1975 Feb;114(2 Pt 1):606-9.
Methods devised for generation and assay of migration inhibitory factor (MIF) on a reduced scale have permitted the performance of experiments which demonstrate that glass bead column-purified guinea pig lymph node lymphocytes do not produce MIF or proliferate in response to antigen. Evidence that the macrophage is the essential cellular element eliminated by the purification procedure is demonstrated by the restoration of both lymphocyte responses upon addition of 5% macrophages to the purified lymphocytes. Autologous, immune and syngeneic, non-immune peritoneal exudate macrophages were equally effective in restoring MF production by purified lymphocytes. Supernatants which inhibited the migration of peritoneal exudate macrophages had only minimal or no effect on the migration of alveolar macrophages, confirming that the inhibitory effects studied were attributable to MF and not cytophilic antibody.
为在较小规模上生成和检测迁移抑制因子(MIF)而设计的方法,使得能够开展实验,这些实验表明,经玻璃珠柱纯化的豚鼠淋巴结淋巴细胞不会产生MIF,也不会对抗原产生增殖反应。通过向纯化淋巴细胞中添加5%的巨噬细胞后淋巴细胞反应得以恢复,证明巨噬细胞是纯化过程中被去除的关键细胞成分。自体、免疫和同基因、非免疫的腹膜渗出巨噬细胞在恢复纯化淋巴细胞产生MF方面同样有效。抑制腹膜渗出巨噬细胞迁移的上清液对肺泡巨噬细胞的迁移只有极小影响或没有影响,这证实所研究的抑制作用归因于MF而非嗜细胞抗体。