Abstract
Purpose of Review
The aim of this manuscript is to review two immune-mediated drug-induced liver injury (DILI) phenotypes, immune-allergic DILI (IA-DILI) and DILI with autoimmune hepatitis features (DILI-AIH), which are poorly defined and can lead to significant morbidity and mortality.
Recent Findings
Recent information on this topic improves the understanding of IA-DILI and DILI-AIH regarding risk factors, associated medications, clinical presentations, histopathologic findings, and management strategies.
Summary
Although the pathogenesis and specific mechanisms remain elusive, clinical and pathological advancements in our understanding of IA-DILI and DILI-AIH have provided clinicians with added tools for the diagnosis and management of these diseases. Further studies are needed to improve our understanding of immune-mediated DILI.
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Abbreviations
- DILI:
-
Drug-induced liver injury
- IA-DILI:
-
Immuno-allergic DILI
- DILI-AIH:
-
Drug-induced autoimmune hepatitis
- I-DILI:
-
Idiosyncratic DILI
- FDA:
-
Food and Drug Administration
- ALF:
-
Acute liver failure
- APC:
-
Antigen-presenting cells
- TCR:
-
T cell receptor
- HLA:
-
Human leukocyte antigen
- NSAID:
-
Nonsteroidal anti-inflammatory drug
- TEN:
-
Toxic epidermal necrolysis
- DRESS:
-
Drug reaction with eosinophilia and systemic symptoms
- ESR:
-
Erythrocyte sedimentation rate
- CRP:
-
C-reactive protein
- CAM/C:
-
Complementary and alternative medications and Chinese medications
- AIH:
-
Autoimmune hepatitis
- ANA:
-
Anti-nuclear antibody
- ASMA:
-
Anti-smooth muscle antibody
- LKM:
-
Liver-kidney mitochondrial
- CYP:
-
Cytochrome P450
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Acknowledgements
This research was supported by the intramural research programs of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) and the National Cancer Institute (NCI) of the National Institutes of Health (NIH).
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Ben L. Da, Gil Ben-Yakov, David Kleiner, and Christopher Koh declare no conflicts of interest.
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Da, B.L., Ben-Yakov, G., Kleiner, D. et al. Drug-Induced Liver Injury: Understanding the Different Immune-Mediated Phenotypes and Clinical Management. Curr Hepatology Rep 17, 235–244 (2018). https://doi.org/10.1007/s11901-018-0407-9
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DOI: https://doi.org/10.1007/s11901-018-0407-9