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Induction of Drug-Induced, Autoimmune Hepatitis in BALB/c Mice for the Study of Its Pathogenic Mechanisms
Published on: May 29, 2020
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Drug-induced autoimmune hepatitis: A minireview
Chin Kimg Tan1, Danielle Ho1, Lai Mun Wang2
1Gastroenterology and Hepatology, Changi General Hospital, Singapore 529889, Singapore.
World Journal of Gastroenterology
|August 18, 2022
Summary
Drug-induced autoimmune hepatitis (DIAIH) can mimic idiopathic autoimmune hepatitis (AIH). Early identification and drug withdrawal are crucial for favorable outcomes in DIAIH.
Area of Science:
- Hepatology
- Immunology
- Pharmacology
Background:
- Drug-induced autoimmune hepatitis (DIAIH) is a significant cause of drug-induced liver injury (DILI).
- DIAIH shares clinical and histological features with idiopathic autoimmune hepatitis (AIH), complicating diagnosis.
- Various drug classes, including antimicrobials, NSAIDs, statins, and anti-TNF agents, are implicated in DIAIH.
Purpose of the Study:
- To highlight the diagnostic challenges and clinical features of DIAIH.
- To present two cases of DIAIH secondary to Sorafenib and Atorvastatin.
- To review the literature on DIAIH and emphasize early identification and management strategies.
Main Methods:
- Case report presentation of two patients with DIAIH.
- Literature review of drug-induced autoimmune hepatitis.
- Analysis of clinical presentation, diagnostic workup, and treatment outcomes.
Main Results:
- The clinical presentation of DIAIH can be indistinguishable from AIH, including positive autoantibodies and elevated immunoglobulin G.
- Liver biopsy may be necessary, with advanced fibrosis favoring idiopathic AIH.
- Cessation of the suspected drug is key, with spontaneous resolution and lack of relapse after steroid taper supporting DIAIH.
Conclusions:
- Early recognition of DIAIH based on drug history and clinical course is vital.
- Prompt drug withdrawal and appropriate management, including corticosteroids if needed, lead to favorable outcomes.
- Distinguishing DIAIH from AIH is critical to avoid unnecessary long-term immunosuppression.
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