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Published on: December 16, 2021
Colitis associated with biological agents
1Division of Gastroenterology, Department of Medicine, University of British Columbia Hospital, Vancouver, BC V6T 1W5, Canada. hugfree@shaw.ca
Abstract:
In the past, there has been considerable focus on a host of drugs and chemicals that may produce colonic toxicity. Now, a variety of new biological monoclonal antibody agents, usually administered by infusion, have appeared in the clinical realm over the last decade or so to treat different chronic inflammatory or malignant disorders.For some of these agents, adverse effects have been documented, including apparently new forms of immune-mediated inflammatory bowel disease. In some, only limited symptoms have been recorded, but in others, severe colitis with serious complications, such as bowel perforation has been recorded. In others, adverse effects may have a direct vascular or ischemic basis, while other intestinal effects may be related to a superimposed infection. Some new onset cases of ulcerative colitis or Crohn's disease may also be attributed to the same agents used to treat these diseases, or be responsible for disease exacerbation. Dramatic and well documented side effects have been observed with ipilimumab, a humanized monoclonal antibody developed to reduce and overcome cytotoxic T-lymphocyte antigen 4, a key negative feedback regulator of the T-cell anti-tumor response. This agent has frequently been used in the treatment of different malignancies, notably, malignant melanoma. Side effects with this agent occur in up to 40% and these are believed to be largely immune-mediated. One of these is a form of enterocolitis that may be severe, and occasionally, fatal. Other agents include rituximab (an anti-CD20 monoclonal antibody), bevacizumab (a monoclonal antibody against the vascular endothelial growth factor) and anti-tumor necrosis factor agents, including infliximab, adalimumab and etanercept.
Insights
New biological monoclonal antibody therapies can cause severe immune-mediated colitis and other gastrointestinal issues. These adverse effects, including new inflammatory bowel disease, require careful monitoring in patients undergoing treatment for chronic inflammatory or malignant disorders.
Area of Science:
- Gastroenterology
- Immunology
- Oncology
Background:
- Monoclonal antibodies are increasingly used to treat chronic inflammatory and malignant conditions.
- These therapies can lead to significant gastrointestinal adverse effects, including immune-mediated colitis.
- Previous research focused on drug-induced colonic toxicity, but new biological agents present novel challenges.
Purpose of the Study:
- To review the emerging adverse effects of biological monoclonal antibody agents on the gastrointestinal tract.
- To highlight the spectrum of colonic toxicity associated with these novel therapies.
- To discuss the mechanisms and clinical implications of these side effects.
Main Methods:
- Literature review of adverse effects associated with monoclonal antibody therapies.
- Analysis of documented cases of gastrointestinal toxicity, including colitis, enterocolitis, and inflammatory bowel disease.
- Categorization of side effects based on potential mechanisms (immune-mediated, vascular, infectious).
Main Results:
- Monoclonal antibodies, such as ipilimumab, rituximab, bevacizumab, and anti-tumor necrosis factor agents, are associated with gastrointestinal adverse events.
- These events can range from mild symptoms to severe colitis, perforation, and even fatal outcomes.
- Immune-mediated mechanisms are implicated in a significant proportion of these side effects, including new-onset or exacerbated inflammatory bowel disease.
Conclusions:
- Biological monoclonal antibody therapies introduce a new spectrum of gastrointestinal toxicity.
- Understanding and monitoring for these immune-mediated effects is crucial for patient safety.
- Further research is needed to elucidate mechanisms and develop management strategies for antibody-induced enterocolitis.
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