Evidence map›Paper›PMID 22997428›Full record

ArticleMolecular & cellular proteomics : MCP2012

Identification of new autoantigens by protein array indicates a role for IL4 neutralization in autoimmune hepatitis.

Chiara Zingaretti, Milena Arigò, Angela Cardaci, Monica Moro, Mariacristina Crosti, Antonella Sinisi, Elisa Sugliano, Cristina Cheroni, Francesco Marabita, Renzo Nogarotto and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Observational
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Developments and Applications of Functional Protein Microarrays.Molecular & cellular proteomics : MCP · 2020
    Review
  15. Article
  16. Article
  17. Review
  18. Autoimmune hepatitis.Frontiers of medicine · 2015
    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

25 authors at 7 institutions in 1 country.

Chiara ZingarettiIstituto Nazionale Genetica Molecolare (INGM), 20122 Milan, Italy.
Milena Arigò
Angela Cardaci
Monica Moro
Mariacristina Crosti
Antonella Sinisi
Elisa Sugliano
Cristina Cheroni
Francesco Marabita
Renzo Nogarotto
Raoul Jean Pierre Bonnal
Paolo Marcatili
Maurizio Marconi
Annalinda Zignego
Paolo Muratori
Pietro Invernizzi
Piero Colombatto
Maurizia Brunetto
Ferruccio Bonino
Raffaele De Francesco
Jens Geginat
Massimiliano Pagani
Luigi Muratori
Sergio Abrignani
Mauro Bombaci
Istituto Nazionale Genetica Molecolare · ITPoliclinico S.Orsola-Malpighi · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale Maggiore · ITSapienza University of Rome · ITUniversity of Florence · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune hepatitis (AIH) is an unresolving inflammation of the liver of unknown cause. Diagnosis requires the exclusion of other conditions and the presence of characteristic features such as specific autoantibodies. Presently, these autoantibodies have relatively low sensitivity and specificity and are identified via immunostaining of cells or tissues; therefore, there is a diagnostic need for better and easy-to-assess markers. To identify new AIH-specific autoantigens, we developed a protein microarray comprising 1626 human recombinant proteins, selected in silico for being secreted or membrane associated. We screened sera from AIH patients on this microarray and compared the reactivity with that of sera from healthy donors and patients with chronic viral hepatitis C. We identified six human proteins that are specifically recognized by AIH sera. Serum reactivity to a combination of four of these autoantigens allows identification of AIH patients with high sensitivity (82%) and specificity (92%). Of the six autoantigens, the interleukin-4 (IL4) receptor fibronectin type III domain of the IL4 receptor (CD124), which is expressed on the surface of both lymphocytes and hepatocytes, showed the highest individual sensitivity and specificity for AIH. Remarkably, patients' sera inhibited STAT6 phosphorylation induced by IL4 binding to CD124, demonstrating that these autoantibodies are functional and suggesting that IL4 neutralization has a pathogenetic role in AIH.

Indexed as

Antibodies, NeutralizingAutoantibodiesAutoantigensBiomarkersHepatitis, AutoimmuneHumansInterleukin-4Interleukin-4 Receptor alpha SubunitLiverPhosphorylationProtein Array AnalysisProtein Structure, TertiaryRecombinant ProteinsSignal TransductionSTAT6 Transcription FactorAntibodies, NeutralizingAutoantibodiesAutoantigensBiomarkersInterleukin-4Interleukin-4 Receptor alpha SubunitRecombinant ProteinsSTAT6 protein, humanSTAT6 Transcription Factor

Identifiers

PMID22997428
PMCPMC3518104
OpenAlexW2138010842

What OpenQuestion holds

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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.