Sp. Kon et al., URINARY C5B-9 EXCRETION AND CLINICAL COURSE IN IDIOPATHIC HUMAN MEMBRANOUS NEPHROPATHY, Kidney international, 48(6), 1995, pp. 1953-1958
Recent reports suggested that the presence of terminal complement comp
lex (C5b-9) in urine from patients with idiopathic membranous nephropa
thy (IMN) may indicate on-going immunological damage. This report docu
ments the relationship between C5b-9 excretion and clinical outcome in
35 adult patients with biopsy-proven IMN and progressively declining
renal function. There were two groups of patients. Group I received on
e of three treatment regimens: prednisolone alone, prednisolone and ch
lorambucil, or prednisolone and cyclophosphamide (N = 22). Group II re
ceived no immunosuppressive therapy (N = 17). Three of the 18 patients
receiving immunosuppressive drugs had more than one treatment regimen
as they experienced a clinical relapse during the study period; hence
22 treatments were available for analysis. Urine samples were collect
ed regularly and urinary C5b-9 (uC5b-9) was determined by ELISA. Both
groups were similar with respect to age, sex distribution, and the dur
ation of follow-up. An improvement in proteinuria and creatinine clear
ance was noted in the immunosuppressed group. Thirty-five patients wer
e excreting C5b-9 initially (18 from group I and 17 from group II); 17
patients continued to excrete C5b-9 at the end of the observation per
iod. These 17 patients had a significantly worse clinical outcome when
compared to the 18 patients whose C5b-9 excretion became negative, ei
ther spontaneously or with treatment (P < 0.005). These results indica
te that continuing C5b-9 excretion is correlated with a poor clinical
outcome. They also suggest that uC5b-9 is a dynamic marker of ongoing
immunological injury, and therefore may be useful in the initial asses
sment and monitoring of patients with IMN and in identifying patients
who may derive benefit from immunosuppressive therapy.