Evidence map›Paper›PMID 19412539›Full record

ArticlePloS one2009

IL10 haplotype associated with tuberculin skin test response but not with pulmonary TB.

Thorsten Thye, Edmund N Browne, Margaret A Chinbuah, John Gyapong, Ivy Osei, Ellis Owusu-Dabo, Norbert W Brattig, Stefan Niemann, Sabine Rüsch-Gerdes, Rolf D Horstmann and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 5 pooled it
2.1field-weighted citation impact, top 14% 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

34 citing papers in PubMed, 5 syntheses or guidelines pooled it, 64 citations in OpenAlex.

  1. Bioscience reports · 2017
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Review
  8. Genetics and evolution of tuberculosis pathogenesis: New perspectives and approaches.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2020
    Review
  9. Review
  10. The Interplay of Human andFrontiers in genetics · 2019
    Review
  11. Review
  12. The Research Progress of Host Genes and Tuberculosis Susceptibility.Oxidative medicine and cellular longevity · 2019
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Genetic Resistance toFrontiers in immunology · 2018
    Review
  18. Article
  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

11 authors at 5 institutions in 2 countries.

Thorsten ThyeBernhard Nocht Institute for Tropical Medicine, Department of Molecular Medicine, Hamburg, Germany. thye@bni-hamburg.de
Edmund N Browne
Margaret A Chinbuah
John Gyapong
Ivy Osei
Ellis Owusu-Dabo
Norbert W Brattig
Stefan Niemann
Sabine Rüsch-Gerdes
Rolf D Horstmann
Christian G Meyer
Bernhard Nocht Institute for Tropical Medicine · DEMinistry of Health · GHResearch Center Borstel - Leibniz Lung Center · DEKumasi Centre for Collaborative Research in Tropical Medicine · GHKwame Nkrumah University of Science and Technology · GH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence from genetic association and twin studies indicates that susceptibility to tuberculosis (TB) is under genetic control. One gene implicated in susceptibility to TB is that encoding interleukin-10 (IL10). In a group of 2010 Ghanaian patients with pulmonary TB and 2346 healthy controls exposed to Mycobacterium tuberculosis, among them 129 individuals lacking a tuberculin skin test (PPD) response, we genotyped four IL10 promoter variants at positions -2849 , -1082 , -819 , and -592 and reconstructed the haplotypes. The IL10 low-producer haplotype -2849A/-1082A/-819C/-592C, compared to the high-producer haplotype -2849G/-1082G/-819C/-592C, occurred less frequent among PPD-negative controls than among cases (OR 2.15, CI 1.3-3.6) and PPD-positive controls (OR 2.09, CI 1.2-3.5). Lower IL-10 plasma levels in homozygous -2849A/-1082A/-819C/-592C carriers, compared to homozygous -2849G/-1082G/-819C/-592C carriers, were confirmed by a IL-10 ELISA (p = 0.016). Although we did not observe differences between the TB patients and all controls, our results provide evidence that a group of individuals exposed to M. tuberculosis transmission is genetically distinct from healthy PPD positives and TB cases. In these PPD-negative individuals, higher IL-10 production appears to reflect IL-10-dependent suppression of adaptive immune responses and sustained long-term specific anergy.

Indexed as

Tuberculin TestBase SequenceCase-Control StudiesDNA PrimersEthnicityFemaleGenetic Predisposition to DiseaseGenetic VariationGhanaHaplotypesHomozygoteHumansImmunity, InnateInterleukin-10MalePromoter Regions, GeneticDNA PrimersIL10 protein, humanInterleukin-10

Identifiers

PMID19412539
PMCPMC2671601
OpenAlexW2028030668

What OpenQuestion holds

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Read underepoch 390

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.