Mathieson P W, Qasim F J, Thiru S, Oldroyd R G, Oliveira D B
Department of Medicine Unit, University of Cambridge, UK.
Clin Exp Immunol. 1994 Sep;97(3):474-7. doi: 10.1111/j.1365-2249.1994.tb06112.x.
Mercuric chloride (HgCl2) induces autoimmunity in susceptible rat strains, with hyper-IgE, appearance of a number of autoantibodies, and widespread tissue injury, including necrotizing vasculitis in the gut. In the early phase of tissue injury there is granulocyte infiltration; later there is immunoglobulin deposition along basement membranes in vessels. We have analysed the role of complement in this model using cobra venom factor (CVF), which causes decomplementation lasting around 5 days. The characteristic time course when HgCl2 is given over 10 days is that tissue injury and autoantibody levels reach a peak at around day 15 (start of HgCl2 = day 0). We therefore gave CVF either early (day 0), intermediate (day 5) or late (day 10); a fourth group (controls) received HgCl2 but no CVF. At each time point, CVF caused complete decomplementation which lasted for at least 5 days. Serum IgE and autoantibody levels were similar in all four experimental groups. Tissue injury in the 'early' CVF group and in the 'late' CVF group was not significantly different from controls, but in the intermediate group tissue injury was significantly more severe than in controls. These data indicate that the complement system does not play a major role in the induction of autoantibodies by HgCl2, nor in the effector phase of tissue injury. We speculate that the exacerbation of tissue injury by CVF in the group given this agent at an intermediate stage of the model is explained by the presence of products of C3 activation which have proinflammatory effects during the phase of active granulocyte-mediated tissue injury.
氯化汞(HgCl2)可在易感大鼠品系中诱发自身免疫反应,表现为高IgE水平、多种自身抗体出现以及广泛的组织损伤,包括肠道坏死性血管炎。在组织损伤的早期阶段有粒细胞浸润;后期血管基底膜有免疫球蛋白沉积。我们使用眼镜蛇毒因子(CVF)分析了补体在该模型中的作用,CVF可导致持续约5天的补体耗竭。当在10天内给予HgCl2时,其特征性的时间进程是组织损伤和自身抗体水平在大约第15天(HgCl2给药开始日=第0天)达到峰值。因此,我们在早期(第0天)、中期(第5天)或晚期(第10天)给予CVF;第四组(对照组)接受HgCl2但不给予CVF。在每个时间点,CVF均导致完全的补体耗竭,且持续至少5天。所有四个实验组的血清IgE和自身抗体水平相似。“早期”CVF组和“晚期”CVF组的组织损伤与对照组无显著差异,但中期组的组织损伤比对照组明显更严重。这些数据表明,补体系统在HgCl2诱导自身抗体产生过程中以及在组织损伤的效应阶段均不发挥主要作用。我们推测,在模型中期给予CVF的组中,CVF加剧组织损伤的原因是C3活化产物的存在,这些产物在活跃的粒细胞介导的组织损伤阶段具有促炎作用。