Evidence map›Paper›PMID 12165073›Full record

ReviewClinical and experimental immunology2002

The immunology of primary biliary cirrhosis: the end of the beginning?

J M Palmer, J A Kirby, D E J Jones

Open access · greenAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Women and primary biliary cirrhosis.Clinical reviews in allergy & immunology · 2015
    Review
  3. Article
  4. Primary biliary cirrhosis.Best practice & research. Clinical gastroenterology · 2010
    Review
  5. Pathogenesis of primary biliary cirrhosis: a unifying model.World journal of gastroenterology · 2006
    Review
  6. 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

3 authors.

J M PalmerCentre for Liver Research, University of Newcastle, Newcastle-upon-Tyne, UK.
J A Kirby
D E J Jones

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chronic liver disease primary biliary cirrhosis (PBC) is characterised by autoreactive B-cell and T-cell responses directed against mitochondrial antigens. In recent years these responses have been extensively characterised and the principal PBC associated autoantigen identified as pyruvate dehydrogenase complex (PDC). The identification of anti-PDC responses (present in over 95% of PDC patients) has given rise to important questions pertinent to our understanding of the pathogenesis of PBC. What specific role to anti-PDC responses play in target cell damage? How and why does immune tolerance break down to as highly conserved and ubiquitously expressed self-antigen as PDC? Why does breakdown in tolerance to an antigen present in all nucleated cells result in damage restricted to the intra-hepatic bile ducts? In attempting to answer these key questions we have, in this review, proposed a unifying hypothesis for the pathogenesis of PBC.

Indexed as

AnimalsAutoantibodiesBiliary TractEpithelial CellsHumansImmunity, CellularLiver Cirrhosis, BiliaryMiceModels, ImmunologicalPyruvate Dehydrogenase ComplexSelf ToleranceT-LymphocytesAutoantibodiesPyruvate Dehydrogenase Complex

Identifiers

PMID12165073
PMCPMC1906441
OpenAlexW2141213451

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.