Evidence map›Paper›PMID 31713023›Full record

ReviewClinical reviews in allergy & immunology2020

Clinical Management of Primary Biliary Cholangitis-Strategies and Evolving Trends.

Lixia Gao, Li Wang, Elena Woo, XiaoSong He, GaoXiang Yang, Christopher Bowlus, Patrick S C Leung, M Eric Gershwin

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical reviews in allergy & immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Dual-tracer PET/CT imaging withRheumatology and immunology research · 2026
    Article
  3. Article
  4. Review
  5. FXR-mediated antigen-specific CD8Journal for immunotherapy of cancer · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Elevated Serum Soluble Tim-3 in Primary Biliary Cholangitis: Lack of Correlation with Cytokines, Chemokines, and Clinical Parameters.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Exosomal Long Noncoding RNAs Serve as Biomarkers for Liver Disease.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Review
  15. Article
  16. Current and future opportunities for the management of primary biliary cholangitis.Frontiers in gastroenterology (Lausanne, Switzerland) · 2023
    Review
  17. Review
  18. Frontiers in immunology · 2022
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Lixia GaoDepartment of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei Province, China.
Li WangDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Science, Beijing, China.
Elena WooDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California, Davis, 451 Health Sciences Drive, Suite 6510, Davis, CA, 95616, USA.
XiaoSong HeDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California, Davis, 451 Health Sciences Drive, Suite 6510, Davis, CA, 95616, USA.
GaoXiang YangDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California, Davis, 451 Health Sciences Drive, Suite 6510, Davis, CA, 95616, USA.
Christopher BowlusDivision of Gastroenterology and Hepatology, School of Medicine, University of California, Davis, CA, 95616, USA.
Patrick S C LeungDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California, Davis, 451 Health Sciences Drive, Suite 6510, Davis, CA, 95616, USA. psleung@ucdavis.edu.ORCID http://orcid.org/0000-0001-5862-4316
M Eric GershwinDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California, Davis, 451 Health Sciences Drive, Suite 6510, Davis, CA, 95616, USA. megershwin@ucdavis.edu.
University of California, Davis · USChinese Academy of Medical Sciences & Peking Union Medical College · CNHebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AnimalsBile Acids and SaltsBiomarkersChenodeoxycholic AcidCombined Modality TherapyDisease ManagementDisease ProgressionDisease SusceptibilityFibrosisHumansImmunotherapyLiver Cirrhosis, BiliaryLiver TransplantationMolecular Targeted TherapySeverity of Illness IndexSymptom AssessmentBile Acids and SaltsBiomarkersChenodeoxycholic Acidobeticholic acidUrsodeoxycholic AcidClinical trialNanomedicinePrimary biliary cholangitisTolerogenic nanoparticle

Identifiers

PMID31713023
OpenAlexW2984629632

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.