Abstract

BackgroundVarious molecular-targeted therapeutic agents that inhibit cytokines and immune checkpoints are used in clinical practice. Some of these biologics that control immunity, such as anti-interleukin-17, anti-programmed cell death protein-1, and anti-cytotoxic T-lymphocyte-associated protein antibodies, affect intestinal immune homeostasis and cause intestinal inflammation. Development of enteritis due to dupilumab (an anti-IL-4Ralpha monoclonal antibody) therapy is not yet reported in the literature.Case presentationA 17-year-old man was administered an injection of dupilumab and continued to receive it for refractory atopic dermatitis. After 3 months of initiating dupilumab therapy, he developed intermittent abdominal pain, tenesmus, and had diarrhea. Colonoscopy examination showed decreased vascularity, mild friability, and erythema in the cecum, part of the ascending colon, sigmoid colon, and rectum without any pathogenic bacteria. Histological examination revealed moderate mixed inflammatory cell infiltration, cryptitis, destruction of the crypt, decreased goblet cells, mucosal erosions, and edema. He was diagnosed with UC and was prescribed oral mesalazine (4800 mg/day) treatment. Within a month of the treatment, his diarrhea improved and the frequency of defecation decreased.ConclusionsThis is a first report that dupilumab mimicked ulcerative colitis. Careful monitoring for adverse effects with the onset of an intestinal inflammation will be recommended after dupilumab administration.

Highlights

  • Various molecular-targeted therapeutic agents that inhibit cytokines and immune checkpoints are used in clinical practice

  • Careful monitoring for adverse effects with the onset of an intestinal inflammation will be recommended after dupilumab administration

  • Molecular-targeted therapeutic agents are innovative therapeutic agents used in several fields, such as cancer and immune diseases, that effectively act on specific molecules and in turn inhibit disease pathways [1, 2]

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Summary

Introduction

Various molecular-targeted therapeutic agents that inhibit cytokines and immune checkpoints are used in clinical practice. Conclusions: This is a first report that dupilumab mimicked ulcerative colitis. Careful monitoring for adverse effects with the onset of an intestinal inflammation will be recommended after dupilumab administration. Various therapeutic agents that inhibit cytokines and immune checkpoints are used in clinical practice.

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