Literature DB >> 35369660

Transforming Growth Factor Beta Receptor 3 (TGFBR3)-Associated Membranous Nephropathy.

Tiffany N Caza1, Samar I Hassen1, Daniel J Kenan1, Aaron Storey2, John M Arthur2, Christian Herzog2, Rick D Edmondson2, T David Bourne1, Laurence H Beck3, Christopher P Larsen1.   

Abstract

Background: Membranous lupus nephritis (MLN) comprises 10%-15% of lupus nephritis and increases morbidity and mortality of patients with SLE through complications of nephrotic syndrome and chronic kidney failure. Identification of the target antigens in MLN may enable noninvasive monitoring of disease activity, inform treatment decisions, and aid in prognostication, as is now possible for idiopathic MN caused by antibodies against the phospholipase A2 receptor. Here, we show evidence for type III TGF-β receptor (TGFBR3) as a novel biomarker expressed in a subset of patients with MLN.
Methods: Mass spectrometry was used for protein discovery through enrichment of glomerular proteins by laser capture microdissection and through elution of immune complexes within MLN biopsy specimens. Colocalization with IgG within glomerular immune deposits from patients and disease controls was evaluated by confocal microscopy. Immunostaining of consecutive case series was used to determine the overall frequency in MN and MLN.
Results: TGFBR3 was found to be enriched in glomeruli and coimmunoprecipitated with IgG within a subset of MLN biopsy specimens by mass spectrometry. Staining of consecutive MN cases without clinical evidence of SLE did not show TGFBR3 expression (zero of 104), but showed a 6% prevalence in MLN (11 of 199 cases). TGFBR3 colocalized with IgG along the glomerular basement membranes in TGFBR3-associated MN, but not in controls. Conclusions: Positive staining for TGFBR3 within glomerular immune deposits represents a distinct form of MN, substantially enriched in MLN. A diagnosis of TGFBR3-associated MN can alert the clinician to search for an underlying autoimmune disease.
Copyright © 2021 by the American Society of Nephrology.

Entities:  

Keywords:  betaglycan; glomerular and tubulointerstitial diseases; mass spectrometry; membranous lupus nephritis; membranous nephropathy; proteoglycans; systemic lupus erythematosus; transforming growth factor beta receptors

Mesh:

Substances:

Year:  2021        PMID: 35369660      PMCID: PMC8676385          DOI: 10.34067/KID.0001492021

Source DB:  PubMed          Journal:  Kidney360        ISSN: 2641-7650


  18 in total

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8.  Neural cell adhesion molecule 1 is a novel autoantigen in membranous lupus nephritis.

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10.  Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney.

Authors:  Rajasree Menon; Edgar A Otto; Austin Kokoruda; Jian Zhou; Zidong Zhang; Euisik Yoon; Yu-Chih Chen; Olga Troyanskaya; Jason R Spence; Matthias Kretzler; Cristina Cebrián
Journal:  Development       Date:  2018-08-30       Impact factor: 6.868

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Review 2.  Cell type-specific mechanistic target of rapamycin-dependent distortion of autophagy pathways in lupus nephritis.

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4.  Clinicopathologic features of non-lupus membranous nephropathy in a pediatric population.

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5.  Editorial: Immune dysfunction in nephrotic syndrome - recent advances and new roads ahead.

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6.  The Alternative Pathway Is Necessary and Sufficient for Complement Activation by Anti-THSD7A Autoantibodies, Which Are Predominantly IgG4 in Membranous Nephropathy.

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