An Indirect Immunofluorescence Method Facilitates Detection of Thrombospondin Type 1 Domain–Containing 7A–Specific Antibodies in Membranous Nephropathy
Author(s) -
Elion Hoxha,
Laurence H. Beck,
Thorsten Wiech,
Nicola M. Tomas,
Christian Probst,
Swantje Mindorf,
Catherine Meyer-Schwesinger,
Gunther Zahner,
Phillip Stahl,
Ruth Schöpper,
Ulf Panzer,
Sigrid Harendza,
Udo Helmchen,
David J. Salant,
Rolf A.K. Stahl
Publication year - 2016
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.2016010050
Subject(s) - membranous nephropathy , thrombospondin , medicine , immunofluorescence , western blot , immunohistochemistry , malignancy , antigen , pathology , antibody , gastroenterology , metastasis , immunology , chemistry , glomerulonephritis , kidney , cancer , biochemistry , matrix metalloproteinase , metalloproteinase , gene
Thrombospondin type 1 domain-containing 7A (THSD7A) is a target antigen identified in adult membranous nephropathy (MN) along with the major antigen phospholipase A 2 receptor 1 (PLA 2 R1). The prevalence of THSD7A-Ab-positive patients is unknown, and it is unclear whether the clinical presentation differs between patients positive for PLA 2 R1-Ab or THSD7A-Ab. We screened serum samples of 1276 patients with MN from three different cohorts for the presence of THSD7A-Ab by Western blot analysis and a newly developed indirect immunofluorescence test (IFT). Compared with Western blot analysis, the IFT had a 92% sensitivity and a 100% specificity. The prevalence of THSD7A-associated MN in a prospective cohort of 345 patients with MN was 2.6%, and most were women. In this cohort, the percentage of patients with THSD7A-associated MN and malignant disease significantly exceeded that of patients with PLA 2 R1-associated MN and malignant disease. In all cohorts, we identified 40 patients with THSD7A-associated MN, eight of whom developed a malignancy within a median time of 3 months from diagnosis of MN. In one patient with THSD7A-associated MN and metastases of an endometrial carcinoma, immunohistochemistry showed THSD7A expression on the metastatic cells and within follicular dendritic cells of the metastasis-infiltrated lymph node. We conclude that the IFT allows sensitive and specific measurement of circulating THSD7A-Ab in patients with MN. Patients with THSD7A-associated MN differ in their clinical characteristics from patients with PLA 2 R1-associated MN, and more intensive screening for the presence of malignancies may be warranted in those with THSD7A-associated MN.
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