Membranous nephropathy:: a family report leading to new pathophysiologic concepts

被引:1
|
作者
Debiec, H
Guigonis, V
Mougenot, B
Haymann, JP
Bensman, A
Deschênes, G
Ronco, P
机构
[1] Hop Tenon, Unite INSERM 489, F-75020 Paris, France
[2] Hop Armand Trousseau, Serv Nephrol Pediat, F-75012 Paris, France
来源
关键词
glomerulonephritis; membranous; nephrotic syndrome; kidney failure; neprilysin; kidney glomerules;
D O I
10.1016/S0001-4079(19)33976-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Membranous glomerulonephritis (MGN) is a major cause of the nephrotic syndrome and chronic renal insufficiency. Studies on the reactivity of nephritogenic antibodies implicated in a case of antenatal MGN led to identify for the first time a target of the immune conflict in glomeruli, neutral endopeptidase (CD10). This enzyme that is restricted to certain tissues, being strongly expressed in the placenta and on glomerular podocytes, is involved in the catabolism of a number of regulatory peptides, particularly those involved in vasomotricity. We showed that the nephritogenic antibodies blocked enzymatic activity and that the mother became immunized at the time of a previous pregnancy because she was neutral endopeptidase-deficient. Two additional families have been identified since then. The pathophysiologic mechanisms that we have unraveled are reminiscent of Rhesus immunization and open up new avenues for therapeutic intervention.
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页码:921 / 932
页数:12
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