Infliximab biosimilar-induced lupus nephritis: A case report

Mod Rheumatol Case Rep. 2023 Dec 29;8(1):74-76. doi: 10.1093/mrcr/rxad061.

Abstract

We present a case of microhematuria, proteinuria and hypocomplementemia which developed in a 55-year-old female who was being treated with an infliximab biosimilar for rheumatoid arthritis. Renal biopsy showed lupus nephritis (ISN/RPS classification class IV + V). Treatment with the infliximab biosimilar was discontinued, and treatment with prednisolone, hydroxychloroquine and abatacept was started, resulting in clinical remission of lupus nephritis and RA. Although tumour necrosis factor-α α inhibitors are known to induce production of autoantibodies, symptoms are usually limited to skin involvement or arthritis, and renal complications are rare. Physicians should be aware of the risk of lupus nephritis and carefully monitor patients for the development of renal involvement during treatment with tumour necrosis factor-α inhibitors.

Keywords: Drug-induced lupus; anti-TNF-α-induced lupus; biosimilar; case report; infliximab.

Publication types

  • Case Reports

MeSH terms

  • Biosimilar Pharmaceuticals* / adverse effects
  • Female
  • Humans
  • Infliximab / adverse effects
  • Kidney / pathology
  • Lupus Nephritis* / diagnosis
  • Lupus Nephritis* / drug therapy
  • Middle Aged
  • Tumor Necrosis Factor-alpha

Substances

  • Infliximab
  • Biosimilar Pharmaceuticals
  • Tumor Necrosis Factor-alpha