Ohi H, Tamano M, Sudo S
Department of Internal Medicine II, Nihon University School of Medicine, Tokyo, Japan.
Am J Kidney Dis. 2001 Aug;38(2):384-9. doi: 10.1053/ajkd.2001.26106.
Membranes used for dialysis therapy activate complement. Complement activation is maximal after initiating dialysis and returns to predialysis values by the end of dialysis. No changes in C3 levels have been detected after dialysis. We hypothesized that although C3 levels were unchanged, C3 activity could be altered by dialysis. We measured complement activation in vitro in serum from patients randomized to dialysis treatments using different types of membranes. The classical pathway was activated with aggregated immunoglobulin G (IgG), and the alternative pathway was activated with inulin. Both the classical and alternative pathways were suppressed after dialysis using cellulose membranes (aggregate IgG, P < 0.01; inulin, P < 0.001). When polyacrylonitrile (PAN) or polyethylene glycol grafted cellulose membranes were used for dialysis, only minor suppression of complement pathways was measured. Levels of the control factor SP-40,40 increased at later times for dialysis using cellulose membranes (P < 0.05). Factor H levels were also greater after dialysis using cellulose membranes compared with PAN membranes (P < 0.05). In summary, cellulose membranes suppress complement activation in serum. One suppressing factor may be the complement control factor SP-40,40.
用于透析治疗的膜会激活补体。补体激活在开始透析后达到最大值,并在透析结束时恢复到透析前的值。透析后未检测到C3水平的变化。我们推测,尽管C3水平未变,但C3活性可能会因透析而改变。我们在体外测量了随机接受不同类型膜透析治疗的患者血清中的补体激活情况。经典途径用聚集的免疫球蛋白G(IgG)激活,替代途径用菊粉激活。使用纤维素膜透析后,经典途径和替代途径均受到抑制(聚集IgG,P < 0.01;菊粉,P < 0.001)。当使用聚丙烯腈(PAN)或聚乙二醇接枝纤维素膜进行透析时,仅检测到补体途径的轻微抑制。使用纤维素膜透析后期,对照因子SP - 40,40的水平升高(P < 0.05)。与PAN膜相比,使用纤维素膜透析后因子H水平也更高(P < 0.05)。总之,纤维素膜可抑制血清中的补体激活。一种抑制因子可能是补体控制因子SP - 40,40。