期刊
JOURNAL OF NEPHROLOGY
卷 31, 期 4, 页码 489-502出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s40620-017-0427-5
关键词
Membranous glomerulonephritis; Immunosuppression; Renal diseases; Glomerulopathies
In the last 10 years, basic science and clinical research have made important contributions to the understanding and management of primary membranous nephropathy (MN). The identification of antibodies directed against the M-type phospholipase A(2) receptor (PLA2R) and thrombospondin type-1 domain-containing 7A protein have added a new perspective on diagnosis, monitoring the immunological activity, predicting prognosis and guiding therapy in patients with primary MN. Mounting evidence suggests that quantification and follow-up of antiPLA2R Abs levels can help in assessing prognosis and evaluate the response to treatment. The kidney disease improving global outcomes guidelines published in 2012 have not been updated. New data on the use of rituximab suggest it should be considered as a potential initial therapy in the treatment of patients with primary MN.
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