S4984 Drug-Induced Colitis in a Patient With Rheumatoid Arthritis on Abatacept Therapy

Introduction: Drug-induced inflammatory colitis encompasses a range of colon disorders that can manifest microscopically or macroscopically. Medications prescribed for rheumatic conditions can trigger flare-ups of inflammatory bowel disease or lead to de novo colitis. Therapeutic monoclonal anti-cytotoxic T-lymphocyte-associated antigen 4 antibodies are associated with immune-mediated enterocolitis. Abatacept, a fusion protein targeting cytotoxic T-lymphocyte-associated antigen 4, is commonly used for rheumatoid arthritis but has been associated with gastrointestinal adverse effects, including enterocolitis. While abatacept-induced colitis is rare, it can resemble Crohn's disease or ulcerative colitis, with symptoms of colonic inflammation, sometimes complicated by fistula formation. This case highlights abatacept-induced colitis and offers guidance for physicians managing such cases—typically involving discontinuation of the suspected medication and treatment with steroids or immune-modulating therapies. Case Description/Methods: A 63-year-old woman with a history of hypertension, hyperlipidemia, and rheumatoid arthritis (treated with leflunomide and abatacept) presented to the emergency department with 12 days of severe, diffuse, crampy abdominal pain and persistent watery diarrhea. Labs revealed leukocytosis (white blood cell 13 × 109/L), with elevated inflammatory markers and liver enzymes. Computed tomography imaging showed ileal and colonic thickening suggestive of inflammatory bowel disease. Stool cultures and serologies were negative for Clostridioides difficile and viral pathogens. Colonoscopy revealed sigmoid and rectal ulcers, with biopsies showing acute and chronic colitis with cryptitis. After excluding infectious causes, abatacept was identified as the likely trigger and was discontinued. The patient was started on Entocort, leading to symptom resolution at follow-up. Discussion: This case highlights the rare but significant potential for abatacept to induce severe colitis in rheumatoid arthritis patients. The pathophysiology involves the suppression of regulatory T cells, which plays a crucial role in maintaining intestinal immune tolerance. Previous cases describe management with drug withdrawal and therapies like mesalamine, infliximab, or steroids. In this case, endoscopic findings and histology supported the diagnosis of abatacept-induced colitis, with improvement after drug cessation. Early colonoscopy and abatacept withdrawal are crucial for patients with suspected drug-induced colitis presenting with diarrhea or gastrointestinal bleeding.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001147396.30668.bb
Primary Topic
Microscopic Colitis
Type
article
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article

S4984 Drug-Induced Colitis in a Patient With Rheumatoid Arthritis on Abatacept Therapy

The American Journal of Gastroenterology
Microscopic Colitis
article

S4984 Drug-Induced Colitis in a Patient With Rheumatoid Arthritis on Abatacept Therapy

article en

Abstract

Introduction: Drug-induced inflammatory colitis encompasses a range of colon disorders that can manifest microscopically or macroscopically. Medications prescribed for rheumatic conditions can trigger flare-ups of inflammatory bowel disease or lead to de novo colitis. Therapeutic monoclonal anti-cytotoxic T-lymphocyte-associated antigen 4 antibodies are associated with immune-mediated enterocolitis. Abatacept, a fusion protein targeting cytotoxic T-lymphocyte-associated antigen 4, is commonly used for rheumatoid arthritis but has been associated with gastrointestinal adverse effects, including enterocolitis. While abatacept-induced colitis is rare, it can resemble Crohn's disease or ulcerative colitis, with symptoms of colonic inflammation, sometimes complicated by fistula formation. This case highlights abatacept-induced colitis and offers guidance for physicians managing such cases—typically involving discontinuation of the suspected medication and treatment with steroids or immune-modulating therapies. Case Description/Methods: A 63-year-old woman with a history of hypertension, hyperlipidemia, and rheumatoid arthritis (treated with leflunomide and abatacept) presented to the emergency department with 12 days of severe, diffuse, crampy abdominal pain and persistent watery diarrhea. Labs revealed leukocytosis (white blood cell 13 × 109/L), with elevated inflammatory markers and liver enzymes. Computed tomography imaging showed ileal and colonic thickening suggestive of inflammatory bowel disease. Stool cultures and serologies were negative for Clostridioides difficile and viral pathogens. Colonoscopy revealed sigmoid and rectal ulcers, with biopsies showing acute and chronic colitis with cryptitis. After excluding infectious causes, abatacept was identified as the likely trigger and was discontinued. The patient was started on Entocort, leading to symptom resolution at follow-up. Discussion: This case highlights the rare but significant potential for abatacept to induce severe colitis in rheumatoid arthritis patients. The pathophysiology involves the suppression of regulatory T cells, which plays a crucial role in maintaining intestinal immune tolerance. Previous cases describe management with drug withdrawal and therapies like mesalamine, infliximab, or steroids. In this case, endoscopic findings and histology supported the diagnosis of abatacept-induced colitis, with improvement after drug cessation. Early colonoscopy and abatacept withdrawal are crucial for patients with suspected drug-induced colitis presenting with diarrhea or gastrointestinal bleeding.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 33%
Microscopic Colitis
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