Evidence map›Paper›PMID 28363639›Full record

ArticleGastroenterology2017

Increased Expression of Cytotoxic T-Lymphocyte-Associated Protein 4 by T Cells, Induced by B7 in Sera, Reduces Adaptive Immunity in Patients With Acute Liver Failure.

Wafa Khamri, Robin D Abeles, Tie Zheng Hou, Amy E Anderson, Ahmed El-Masry, Evangelos Triantafyllou, Christine Bernsmeier, Fin S Larsen, Arjuna Singanayagam, Nobuaki Kudo and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  8. Suppressor CD4Gut · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Therapeutic plasma exchange in liver failure.World journal of hepatology · 2021
    Review
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  15. Article
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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

20 authors at 6 institutions in 2 countries.

Wafa KhamriDivision of Digestive Diseases, Imperial College London, United Kingdom. Electronic address: w.khamri@imperial.ac.uk.
Robin D AbelesInstitute of Liver Studies, King's College London, United Kingdom.
Tie Zheng HouInstitute of Immunity and Transplantation, University College London, United Kingdom.
Amy E AndersonInstitute of Cellular Medicine, Newcastle University, Newcastle, United Kingdom.
Ahmed El-MasryDivision of Digestive Diseases, Imperial College London, United Kingdom.
Evangelos TriantafyllouDivision of Digestive Diseases, Imperial College London, United Kingdom.
Christine BernsmeierInstitute of Liver Studies, King's College London, United Kingdom.
Fin S LarsenDepartment of Hepatology, Rigshospitalet, Copenhagen, Denmark.
Arjuna SinganayagamInstitute of Liver Studies, King's College London, United Kingdom.
Nobuaki KudoInstitute of Reproductive and Developmental Biology, Imperial College London, United Kingdom.
Lucia A PossamaiDivision of Digestive Diseases, Imperial College London, United Kingdom.
Fanny LebosseDivision of Digestive Diseases, Imperial College London, United Kingdom.
Georg AuzingerInstitute of Liver Studies, King's College London, United Kingdom.
William BernalInstitute of Liver Studies, King's College London, United Kingdom.
Christopher WillarsInstitute of Liver Studies, King's College London, United Kingdom.
Christopher J WestonCentre for Liver Research and National Institute for Health Research, Biomedical Research Unit, University of Birmingham, United Kingdom.
Giovanna LombardiMedical Research Council Centre for Transplantation, King's College London, United Kingdom.
Julia WendonInstitute of Liver Studies, King's College London, United Kingdom.
Mark ThurszDivision of Digestive Diseases, Imperial College London, United Kingdom.
Charalambos G AntoniadesDivision of Digestive Diseases, Imperial College London, United Kingdom; Institute of Liver Studies, King's College London, United Kingdom.
King's College London · GBImperial College London · GBNational Institute for Health Research · GBNewcastle University · GBRigshospitalet · DKUniversity College London · GB

Funding

Medical Research Council G1000344Medical Research Council MR/K010514/1
6 · The paper itself

Abstract

BACKGROUND &

aimsPatients with acute liver failure (ALF) have defects in innate immune responses to microbes (immune paresis) and are susceptible to sepsis. Cytotoxic T-lymphocyte-associated protein 4 (CTLA4), which interacts with the membrane receptor B7 (also called CD80 and CD86), is a negative regulator of T-cell activation. We collected T cells from patients with ALF and investigated whether inhibitory signals down-regulate adaptive immune responses in patients with ALF.

methodsWe collected peripheral blood mononuclear cells from patients with ALF and controls from September 2013 through September 2015 (45 patients with ALF, 20 patients with acute-on-chronic liver failure, 15 patients with cirrhosis with no evidence of acute decompensation, 20 patients with septic shock but no cirrhosis or liver disease, and 20 healthy individuals). Circulating CD4

resultsPeripheral blood samples from patients with ALF had a higher proportion of CD4

conclusionsPeripheral CD4

Indexed as

Adaptive ImmunityAcetaminophenAcute-On-Chronic Liver FailureAdultAnimalsAntibodiesB7-1 AntigenCD3 ComplexCD4 Lymphocyte CountCD4-Positive T-LymphocytesCell ProliferationCells, CulturedChemical and Drug Induced Liver InjuryCoculture TechniquesCTLA-4 AntigenDendritic CellsAcetaminophenAntibodiesB7-1 AntigenCD3 ComplexCTLA-4 AntigenCTLA4 protein, humanImmune RegulationInfection SusceptibilityLiver DiseaseTreatment

Identifiers

PMID28363639
PMCPMC5516432
OpenAlexW2602137310

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.