Infliximab biosimilar-induced lupus nephritis: A case report

Author:

Shidahara Kenta1,Katsuyama Takayuki1ORCID,Hirose Kei1,Matsumoto Kazuya1,Nawachi Shoichi1,Nakadoi Takato1,Asano Yosuke1,Katayama Yu1,Miyawaki Yoshia1,Katsuyama Eri1,Takano-Narazaki Mariko1,Matsumoto Yoshinori1,Sada Ken-Ei12,Wada Jun1

Affiliation:

1. Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences , Okayama, Japan

2. Department of Clinical Epidemiology, Kochi Medical School, Kochi University , Nankoku, Japan

Abstract

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.

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Renal disease in pediatric rheumatology;Current Opinion in Rheumatology;2024-05-17

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