IgA vasculitis during secukinumab therapy

Clin Rheumatol. 2021 May;40(5):2071-2073. doi: 10.1007/s10067-020-05364-1. Epub 2020 Aug 29.

Abstract

Psoriatic arthritis is a chronic, seronegative spondyloarthropathy associated with psoriasis, depending on patient presentation treatment options range from non-pharmacologic measures to NSAIDs, DMARDs, and biologics. Secukinumab is a human monoclonal antibody that specifically targets interleukin-17 and has been shown to be highly effective in the treatment of psoriatic arthritis. As the use of IL-17 inhibitors has been approved in the treatment of psoriatic arthritis, clinicians need to be aware of unusual adverse events not previously observed in clinical trials. We report a rare case of Henoch-Schönlein purpura vasculitis induced by secukinumab in a 39-year-old patient. Therefore, using biologic drugs in clinical practice should be aware that cutaneous vasculitis may be triggered by anti-IL17 treatment, and early diagnosis always helps to decrease morbidity and reduce the amount of time to recovery as well as the impact on the quality of life disruption.

Keywords: Biologics; Henoch-Schönlein purpura; IL-17; Psoriatic arthritis; Rheumatology; Secukinumab.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Antibodies, Monoclonal, Humanized
  • Arthritis, Psoriatic* / drug therapy
  • Humans
  • Immunoglobulin A
  • Quality of Life
  • Vasculitis*

Substances

  • Antibodies, Monoclonal, Humanized
  • Immunoglobulin A
  • secukinumab