Clinical Management of Primary Biliary Cholangitis—Strategies and Evolving Trends
Abstract
PBC is a chronic progressive autoimmune disorder involving the destruction of intrahepatic small bile ducts, cholestasis, fibrosis, and ultimately cirrhosis if left untreated. It is largely driven by the autoimmune response, but bile acids and the intestinal microbiota are implicated in disease progression as well. The only drugs licensed for PBC are UDCA and OCA. UDCA as a first-line and OCA as a second-line therapy are safe and effective, but the lack of response in a significant portion of patients and inadequate control of symptoms such as fatigue and pruritus remain as concerns. Liver transplantation is an end-stage therapy for many patients refractory to UDCA, which gives excellent survival rates but also moderate to high recurrence rates. The limited options for FDA-approved PBC therapies necessitate the development of alternative approaches. Currently, a wide variety of experimental drugs exist targeting immunological and physiological aspects of PBC to suppress inflammation. Immunological therapies include drugs targeting immune molecules in the B cell and T cell response, and specific cytokines and chemokines implicated in inflammation. Drugs targeting bile acids are also noteworthy as bile acids can perpetuate hepatic inflammation and lead to fibrosis over time. These include FXR agonists, ASBT inhibitors, and PPAR agonists such as bezafibrate and fenofibrate. Nonetheless, many of these drugs can only delay disease progression and fail to enhance patients' quality of life. Nanomedicine shows great potential for treatment of autoimmune diseases, as it provides a new approach that focuses on tolerance induction rather than immunosuppression. Tolerogenic nanoparticles carrying immune-modifying agents can be engineered to safely and effectively target the antigen-specific immune response in autoimmune diseases. These may work well with PBC especially, given the anatomical features and immunological specificity of the disease. Nanobiological therapy is thus an area of highly promising research for future treatment of PBC.
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Based on the POISE trial results, OCA received approval as a second-line treatment for PBC in patients with an inadequate response or intolerance to UDCA.
“Based on the POISE trial results, OCA received approval as a second-line treatment for PBC in patients with an inadequate response or intolerance to UDCA [29,30].”
From Second-Line Therapies in Primary Biliary Cholangitis: A Comparative Review of Obeticholic Acid, Fibrates, Seladelpar, and Elafibranor (2025) · cites this paper as [30]
Obeticholic acid (OCA) was approved as a second-line agent by the FDA in May 2016.
“In May 2016, obeticholic acid (OCA) was approved as a second-line agent by the Food and Drug Administration (FDA).”
From Second-Line Therapies in Primary Biliary Cholangitis: A Comparative Review of Obeticholic Acid, Fibrates, Seladelpar, and Elafibranor (2025) · cites this paper as [30]
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References 150 · Cited by 39
- Authors
- Gao, L., Wang, L., Woo, E., He, X., Yang, G., Bowlus, C., Leung, P. S. C., & Gershwin, M. E.
- Affiliations
- Second Hospital of Hebei Medical University (CN)
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- University of California, Davis (US)
- Corresponding author
- Leung, Patrick S.C
- Gershwin, M. Eric
- Venue
- Clinical Reviews in Allergy & Immunology
- Published
- 2019-11-11
- Volume
- 59
- Issue
- 2
- Pages
- 175-194
- ISSN
- 1080-0549 (ISSN-L)
- 1559-0267
- OpenAlex
- W2984629632
- Cited by
- 39
- References
- 150
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 4 · 2023: 9 · 2022: 6 · 2021: 6 · 2020: 4
- FWCI
- 0.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Reviews in Allergy & Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Health Sciences › Medicine › Surgery › Pediatric Hepatobiliary Diseases and Treatments
- Keywords
- primary biliary cirrhosis, ursodeoxycholic acid, obeticholic acid, liver transplantation, bile acids, gut microbiota, FXR agonists, PPAR agonists, nanomedicine, autoimmune liver disease, cholestasis, fibrosis, fatigue, pruritus
- MeSH terms
- Animals, Bile Acids and Salts, Chenodeoxycholic Acid, Combined Modality Therapy, Disease Susceptibility, Fibrosis, Humans, Immunotherapy, Liver Cirrhosis, Biliary, Severity of Illness Index, Ursodeoxycholic Acid, Biomarkers, Liver Transplantation, Treatment Outcome, Disease Progression, Disease Management, Molecular Targeted Therapy, Symptom Assessment
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