Evidence map›Paper›PMID 26254778›Full record

Observational studyInflammopharmacology2015

T-bet and interleukin-27: possible TH1 immunomodulators of sarcoidosis.

Wei Sheng Joshua Loke, Araluen Freeman, Linda Garthwaite, Silvie Prazakova, Mijeong Park, Kenneth Hsu, Paul S Thomas, Cristan Herbert

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Inflammopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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 1 institution in 2 countries.

Wei Sheng Joshua LokeSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. joshua_loke_w_s@hotmail.com.ORCID http://orcid.org/0000-0001-6496-1546
Araluen FreemanSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. araluen.freeman@unsw.edu.au.
Linda GarthwaiteSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. l.garthwaite@unsw.edu.au.
Silvie PrazakovaSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. s.prazakova@unsw.edu.au.
Mijeong ParkSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. mijeong.park@unsw.edu.au.
Kenneth HsuSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. k.hsu@unsw.edu.au.
Paul S ThomasSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. paul.thomas@unsw.edu.au.
Cristan HerbertSchool of Medical Sciences, Inflammation and Infection Research Centre, UNSW, Sydney, 2052, Australia. c.herbert@unsw.edu.au.
UNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSarcoidosis has often been termed an "immune paradox" as there is peripheral anergy to common recall antigens despite pronounced TH1-dominant inflammation at disease sites, such as the lung, with up-regulation of interferon γ, IL-27 and transcription factors. Peripheral blood may reflect the anergic state, while exhaled breath condensate (EBC) analysis may offer insights into the lung disease.

methodsA cross-sectional study was conducted to investigate the expression of TH1 cytokines and transcription factors (IFNγ, IL-27 and T-bet) in the peripheral blood and/or EBC of sarcoidosis patients and healthy controls. Whole blood and EBC were collected from sarcoidosis patients and healthy controls. TH1 cytokine expression levels were then measured in peripheral blood mononuclear cells (PBMCs) and/or plasma and EBC using quantitative real-time PCR, ELISA and via Western blotting.

resultsCompared to healthy controls, PBMC IL-27 mRNA was higher in patients (p = 0.0019). There were no significant differences in plasma IL-27 protein between patients and controls (p = 0.20). T-bet mRNA and protein were lower (p = 0.010 and p = 0.0043, respectively) in patients compared to controls. There were no significant differences in PBMC IFNγ mRNA and protein expression (p = 0.68 and p = 0.74, respectively) nor in EBC IL-27 levels.

conclusionsOur data indicate that depressed T-bet mRNA and protein expression could contribute to the peripheral anergy in sarcoidosis and that IL-27 mRNA levels are elevated in the PBMC from those with sarcoidosis.

Indexed as

AdultCross-Sectional StudiesFemaleHumansImmunologic FactorsInterleukinsLeukocytes, MononuclearMaleMiddle AgedSarcoidosisT-bet Transcription FactorT-Box Domain ProteinsTh1 CellsYoung AdultImmunologic FactorsInterleukinsMYDGF protein, humanT-bet Transcription FactorT-Box Domain ProteinsAnergyIL-27Interferon-γSarcoidosisT-betTH1

Identifiers

PMID26254778
PMCPMC4568011
OpenAlexW1954785758

What OpenQuestion holds

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LicenceCC BY
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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.