Cited by 39Liver Diseases and ImmunityDrug Transport and Resistance MechanismsPediatric Hepatobiliary Diseases and Treatments

Clinical Management of Primary Biliary Cholangitis—Strategies and Evolving Trends

Gao, Lixia, Wang, Li, Woo, Elena, He, XiaoSong, Yang, GaoXiang, Bowlus, Christopher, Leung, Patrick S.C, Gershwin, M. Eric·2020·Clinical Reviews in Allergy & Immunology

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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Crossref · 10.1007/s12016-019-08772-7

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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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