Novel Antigens and Clinical Updates in Membranous Nephropathy

被引:3
|
作者
Avasare, Rupali [1 ]
Andeen, Nicole [2 ]
Beck, Laurence [3 ,4 ]
机构
[1] Oregon Hlth & Sci Univ, Div Nephrol & Hypertens, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Pathol, Portland, OR 97201 USA
[3] Boston Med Ctr, Dept Med, Sect Nephrol, Boston, MA USA
[4] Boston Univ, Chobanian & Avedisian Sch Med, Sect Nephrol, Dept Med, Boston, MA USA
来源
ANNUAL REVIEW OF MEDICINE | 2024年 / 75卷
关键词
membranous nephropathy; kidney disease; podocyte antigens; nephrotic syndrome; autoimmunity; antibody-mediated kidney disease; PHOSPHOLIPASE A(2) RECEPTOR; DOMAIN-CONTAINING; 7A; RITUXIMAB; AUTOANTIBODIES; TARGET;
D O I
10.1146/annurev-med-050522-034537
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Membranous nephropathy (MN), an autoimmune kidney disease and leading cause of nephrotic syndrome, leads to kidney failure in up to one-third of affected individuals. Most MN cases are due to an autoimmune reaction against the phospholipase A2 receptor (PLA2R) located on kidney podocytes. Serum PLA2R antibody quantification is now part of routine clinical practice because antibody titers correlate with disease activity and treatment response. Recent advances in target antigen detection have led to the discovery of more than 20 other podocyte antigens, yet the clinical impact of additional antigen detection remains unknown and is under active investigation. Here we review recent findings and hypothesize how current research will inform future care of patients with MN.
引用
收藏
页码:219 / 232
页数:14
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