Rubin A S, Macdonald A B
Immunology. 1976 Jan;30(1):69-81.
The mixing of two histoincompatible human lymphocyte cell lines generated the release of a soluble factor which was capable on non-specifically enhancing the in vitro immune response of normal mouse spleen cells against sheep erythrocytes. The mediator was secreted into the supernatant of the allogeneic cell cultures within 24 h of cultuvation. The human enhancing factor (HEF) must be added to assay cultures on day 2, of a 5-day culture period, for its activity to be manifest. HEF was resistant to DNase, RNase and heating at 56 degrees for 30 min, but was inactivated by exposure to protease or elevated temperature (80 degrees for 30 min). The molecular weight of HEF, purified by ammonium sulphate fractionation, followed by Sephadex gel filtration, DEAE-cellulose chromatography and SDS-polyacrylamide gel electrophoresis, was approximately 38,000 Daltons.
两种组织不相容的人淋巴细胞系混合后,可释放出一种可溶性因子,该因子能够非特异性地增强正常小鼠脾细胞对绵羊红细胞的体外免疫反应。在培养24小时内,该介质分泌到同种异体细胞培养物的上清液中。在为期5天的培养期的第2天,必须添加人增强因子(HEF)到检测培养物中,其活性才能显现出来。HEF对脱氧核糖核酸酶、核糖核酸酶以及在56摄氏度下加热30分钟具有抗性,但暴露于蛋白酶或高温(80摄氏度30分钟)会使其失活。通过硫酸铵分级分离、随后的葡聚糖凝胶过滤、二乙氨基乙基纤维素色谱法和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳纯化的HEF分子量约为38,000道尔顿。