Primary IgA Vasculitis with Nephritis in a Patient with Rheumatoid Arthritis Diagnosed by Anti-galactose-deficient IgA1 Immunostaining

Intern Med. 2019 Sep 1;58(17):2551-2554. doi: 10.2169/internalmedicine.2640-19. Epub 2019 Jun 7.

Abstract

Renal disease is a common complication of rheumatoid arthritis (RA) and can occur secondary to RA or be induced by therapeutic agents. Recently, glomerular deposition of galactose-deficient IgA1 (Gd-IgA1) was identified as a feature of primary IgA vasculitis with nephritis (IgA-VN). We herein report a case of IgA-VN in an RA patient whose disease activity was controlled by treatment with etanercept. To distinguish between primary IgA-VN and secondary IgA-VN caused by RA or etanercept, we performed immunostaining of renal biopsy sections with the Gd-IgA1-specific antibody KM55. Positive KM55 staining confirmed the diagnosis of primary IgA-VN in a patient with RA.

Keywords: IgA vasculitis with nephritis; anti-galactose-deficient IgA1 antibody; nephrotic syndrome; rheumatoid arthritis.

Publication types

  • Case Reports

MeSH terms

  • Antirheumatic Agents / therapeutic use
  • Arthritis, Rheumatoid / complications*
  • Arthritis, Rheumatoid / drug therapy
  • Etanercept / therapeutic use
  • Female
  • Galactose / immunology
  • Glomerulonephritis, IGA / diagnosis*
  • Glomerulonephritis, IGA / etiology
  • Glomerulonephritis, IGA / immunology
  • Humans
  • IgA Vasculitis / diagnosis*
  • IgA Vasculitis / etiology
  • IgA Vasculitis / immunology
  • Immunoglobulin A / analysis*
  • Middle Aged

Substances

  • Antirheumatic Agents
  • Immunoglobulin A
  • Etanercept
  • Galactose