Evidence map›Paper›PMID 27379100›Full record

ArticleFrontiers in immunology2016

Combined Expression of IFN-γ, IL-17, and IL-4 mRNA by Recall PBMCs Moderately Discriminates Active Tuberculosis from Latent Mycobacterium tuberculosis Infection in Patients with Miscellaneous Inflammatory Underlying Conditions.

Laura E Savolainen, Anu Kantele, Aija Knuuttila, Liana Pusa, Riitta Karttunen, Heikki Valleala, Tamara Tuuminen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Specific immune response toFrontiers in immunology · 2024
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  3. Diagnostic Performance of a NovelFrontiers in microbiology · 2022
    Article
  4. Frontiers in immunology · 2021
    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

7 authors at 3 institutions in 1 country.

Laura E SavolainenDepartment of Bacteriology and Immunology, Haartman Institute, University of Helsinki , Helsinki , Finland.
Anu KanteleDepartment of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Helsinki, Finland; Department of Medicine, Division of Infectious Diseases, Helsinki University Central Hospital, Helsinki, Finland; Department of Medicine, Institute of Clinical Medicine, University of Helsinki, Helsinki, Finland.
Aija KnuuttilaHeart and Lung Center, Helsinki University Central Hospital , Helsinki , Finland.
Liana PusaLänsi-Uusimaa Hospital , Tammisaari , Finland.
Riitta KarttunenDepartment of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Helsinki, Finland; Laboratory Division (HUSLAB), Helsinki University Central Hospital, Helsinki, Finland.
Heikki VallealaDepartment of Medicine, Division of Rheumatology, Helsinki University Central Hospital , Helsinki , Finland.
Tamara TuuminenDepartment of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Helsinki, Finland; Eastern Finland Laboratory Centre Joint Authority Enterprise, Mikkeli, Finland.
University of Helsinki · FIHelsinki University Hospital · FISitra · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New biomarkers are needed for discriminating active tuberculosis (TB) from latent TB infection (LTBI), especially in vulnerable groups representing the major diagnostic challenge. This pilot study was carried out to explore the diagnostic potential of selected genes, IFN-γ, IL-17, IL-4, and FoxP3, associated with TB immunity and immunopathology. IFN-γ, IL-17, IL-4, and FoxP3 mRNA expression levels were measured by quantitative reverse transcription PCR (RT-qPCR) from antigen-stimulated peripheral blood mononuclear cells of patients with active TB (n = 25); patients with miscellaneous inflammatory disorders and concomitant LTBI (n = 20), rheumatoid arthritis (RA) being the most predominant in the group (n = 11); and in healthy Bacillus Calmette-Guérin (BCG) vaccinees (n = 8). While the levels of FoxP3 mRNA did not differ between the tested groups, the cumulative expression levels of purified protein derivative-stimulated IFN-γ, IL-17, and IL-4 mRNAs were found to distinguish active TB from the whole group of LTBI with 48% sensitivity and 85% specificity. When restricting the LTBI group to RA cases only, the sensitivity was 56% and specificity 100%. When interpreting the result as positive in at least one of the mRNAs IFN-γ, IL-17, or IL-4, sensitivity of 64% and specificities of 75% (heterogeneous group of LTBI) or 100% (LTBI with RA) were achieved. Moderate discrimination of active TB from LTBI with miscellaneous inflammatory underlying conditions by using combined quantitative expression of IFN-γ, IL-17, and IL-4 mRNA seems not to be of high diagnostic potential.

Indexed as

active TBIFN-γIL-17IL-4LTBImRNA

Identifiers

PMID27379100
PMCPMC4905973
OpenAlexW2432281414

What OpenQuestion holds

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Registered trials

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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.