Scher M G, Beller D I, Unanue E R
J Exp Med. 1980 Dec 1;152(6):1684-98. doi: 10.1084/jem.152.6.1684.
Previous studies have shown that Listeria monocytogenes-immune T cells, adoptively transferred into normal mice with killed Listeria organisms, induced peritoneal exudates rich in Ia-positive macrophages. We show now that culture fluids generated by Listeria-immune exudate cells and Listeria contain an activity that elicits Ia-rich exudates when injected intraperitoneally. The factor that recruits Ia-positive macrophages must be injected several times during a 2-d period for optimal demonstration of its activity. The induction of the factor is immunologically specific and requires Ia-positive macrophages, primed T lymphocytes, and antigen challenge. The factor is a nondialyzable protein and is not genetically restricted in its activity. The macrophages in the exudates induced by the factor bear Fc receptors, take up latex, synthesize I-A, but bear few C3 receptors. We have thus identified an immune mediator capable of controlling the Ia phenotype of the exudate macrophages.
先前的研究表明,将单核细胞增生李斯特菌免疫的T细胞,与杀死的李斯特菌一起过继转移到正常小鼠体内,会诱导出富含Ia阳性巨噬细胞的腹腔渗出液。我们现在表明,由李斯特菌免疫渗出细胞和李斯特菌产生的培养液含有一种活性物质,当腹腔注射时会引发富含Ia的渗出液。在2天的时间内必须多次注射招募Ia阳性巨噬细胞的因子,才能最佳地显示其活性。该因子的诱导具有免疫特异性,需要Ia阳性巨噬细胞、致敏的T淋巴细胞和抗原激发。该因子是一种不可透析的蛋白质,其活性不受基因限制。由该因子诱导的渗出液中的巨噬细胞带有Fc受体,摄取乳胶,合成I-A,但几乎没有C3受体。因此,我们鉴定出一种能够控制渗出液巨噬细胞Ia表型的免疫介质。