Leibowitch J, Halbwachs L, Wattel S, Gaillard M H, Droz D
Kidney Int. 1979 Apr;15(4):396-403. doi: 10.1038/ki.1979.51.
Dense deposit disease of the kidney is a rare form of chronic glomerulonephritis frequently associated with serum complement abnormalities (low C3 levels) and a circulating C3 convertase activator of the alternative pathway, the C3 nephritic factor (NF). Eleven patients with end-stage dense deposit disease underwent kidney transplantation. Of the 11, 7 had pretransplant low C3 and NF. In the posttransplant period, persisting low C3 levels were associated with persisting NF, although not quantitatively so. The original glomerular lesion recurred in the graft within 6 months in 9 of 11. Of these 9, 2 had no complement abnormalities either prior to or after transplantation. Pretransplant complement abnormalities were rapidly corrected in 4 of 7 patients whether or not recurrence of the original lesion occurred. Thus, serum complement profiles before and after transplantation are neither predictive nor indicative of recurrence.
肾致密沉积物病是一种罕见的慢性肾小球肾炎,常与血清补体异常(C3水平降低)以及替代途径的循环C3转化酶激活剂即C3肾炎因子(NF)相关。11例终末期致密沉积物病患者接受了肾移植。在这11例患者中,7例移植前C3和NF水平较低。在移植后时期,持续的低C3水平与持续的NF相关,尽管在数量上并非如此。11例中有9例移植肾在6个月内出现了原有的肾小球病变复发。在这9例中,2例移植前后均无补体异常。7例患者中有4例移植前的补体异常无论原发病变是否复发均迅速得到纠正。因此,移植前后的血清补体情况既不能预测也不能指示复发。