抗原
膜性肾病
免疫学
奈特林
医学
小学(天文学)
肾小球肾炎
肾
内科学
受体
轴突引导
天文
物理
作者
Linda Reinhard,Maya Machalitza,Thorsten Wiech,Hermann‐Josef Gröne,Moritz Lassé,Markus M. Rinschen,Nicoletta Ferru,Jan Hinrich Bräsen,Friederike Drömann,Peter Rob,Sanjeev Sethi,Elion Hoxha,Rolf A.K. Stahl
出处
期刊:Journal of The American Society of Nephrology
日期:2022-08-19
卷期号:33 (10): 1823-1831
被引量:40
标识
DOI:10.1681/asn.2022050608
摘要
Background: Primary membranous nephropathy (MN) is caused by circulating autoantibodies (ab) binding to antigens on the podocyte surface. PLA2R1 is the main target antigen in 70-80% of cases, but the pathogenesis is unresolved in 10-15% of patients. Methods: We used native Western blotting to identify IgG4-ab in the serum of the index MN patient, which binds an antigen endogenously expressed on podocyte membranes. These IgG4-ab were used to immunoprecipitate the target antigen and mass spectrometry used to identify Netrin G1 (NTNG1). Native Western blot and ELISA analyzed NTNG1-ab in cohorts of 888 patients with MN or other glomerular diseases. Results: NTNG1 was identified as a novel target antigen in MN. It is a membrane protein expressed in healthy podocytes. Immunohistochemistry confirmed granular NTNG1 in subepithelial glomerular immune deposits. In prospective and retrospective MN cohorts, we identified three patients with NTNG1-associated MN, who showed IgG4-dominant circulating NTNG1-ab, enhanced NTNG1 expression in the kidney, and glomerular IgG4 deposits. No NTNG1-ab were identified in 561 PLA2R1-ab positive patients, 27 THSD7A-ab positive patients, and 77 patients with other glomerular diseases. In two patients with available followup of 2 and 4 years, both NTNG1-ab and proteinuria persisted. Conclusions: NTNG1 expands the repertoire of target antigens in patients with MN. The clinical role of NTNG1-ab remains to be defined.
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