Karanikas V, Mackay I R, Rowley M J, Loveland B E
Centre for Molecular Biology and Medicine, Monash University, Clayton, Victoria, Australia.
Cell Immunol. 1993 Apr 15;148(1):166-76. doi: 10.1006/cimm.1993.1099.
We investigated whether a novel immunisation scheme using an endogenous protein could stimulate an autoreactive cytolytic response. The protein selected was porcine dihydrolipoamide dehydrogenase, the E3 component of the mitochondrial 2-OADC enzyme family, because it is structurally conserved in mammals and ubiquitously expressed. Recombinant insulin was used as an alternative antigen. Female BALB/c mice were injected with adjuvant-free syngeneic lymphoid cells that had been exposed to E3 in hypertonic medium to facilitate its pinocytosis and were given two booster injections. Effector lymphoid cells from immunised mice were cultured in vitro with irradiated syngeneic cells that had been treated with hypertonic medium, either with or without antigen. Cytolytic effector cells were detected that lysed isogeneic and not allogeneic target cells, but only from mice immunised with E3. This experimental system provides a new model for the early stages of the development of autoimmunity.
我们研究了一种使用内源性蛋白质的新型免疫方案是否能刺激自身反应性溶细胞反应。所选蛋白质为猪二氢硫辛酰胺脱氢酶,它是线粒体2 - 氧代酸脱氢酶家族的E3成分,因为它在哺乳动物中结构保守且普遍表达。重组胰岛素用作替代抗原。雌性BALB/c小鼠注射了无佐剂的同基因淋巴细胞,这些淋巴细胞在高渗培养基中暴露于E3以促进其胞饮作用,并给予两次加强注射。将免疫小鼠的效应淋巴细胞与经高渗培养基处理的照射过的同基因细胞在体外培养,有无抗原均可。检测到溶细胞效应细胞能裂解同基因而非异基因靶细胞,但仅来自用E3免疫的小鼠。该实验系统为自身免疫发展的早期阶段提供了一个新模型。