Evidence map›Paper›PMID 22788220›Full record

ArticleCellular microbiology2012

Natural killer cells are recruited during pulmonary tuberculosis and their ex vivo responses to mycobacteria vary between healthy human donors in association with KIR haplotype.

Damien Portevin, Laura E Via, Seokyong Eum, Douglas Young

Open access · greenAbstract read
In one paragraph

Article in Cellular microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

39 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Pharmacogenomic heterogeneity ofAnnals of medicine · 2025
    Observational
  3. Article
  4. Article
  5. Variants in theJournal of clinical tuberculosis and other mycobacterial diseases · 2024
    Article
  6. Article
  7. Cystatin F Depletion inInternational journal of molecular sciences · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Initial immune response after exposure toFrontiers in immunology · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Observational
  17. TheFuture virology · 2020
    Review
  18. Article
  19. Distinct Human NK Cell Phenotypes and Functional Responses toFrontiers in cellular and infection microbiology · 2020
    Article
  20. Review
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

4 authors at 2 institutions in 2 countries.

Damien PortevinDivision of Mycobacterial Research, MRC National Institute for Medical Research, The Ridgeway, Mill Hill, London, UK. dportev@nimr.mrc.ac.uk
Laura E Via
Seokyong Eum
Douglas Young
International Tuberculosis Research Center · KRNational Institutes of Health · US

Funding

International Research in Korea: Clinical Studies of Drug-Resistant TuberculosisZIAAI001067 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BARRY, CLIFTON · 2009 to 2017
$6.9M
Intramural NIH HHSMedical Research Council MC_U117581288Medical Research Council U117581288
6 · The paper itself

Abstract

Humans vary widely in their susceptibility to tuberculosis. While only a minority will progress to disease, the majority of healthy individuals exposed to Mycobacterium tuberculosis mount an immune response that can clear or contain the infection in a quiescent form. Using immunofluorescence on human clinical samples, we identified natural killer (NK) cells infiltrating granulomatous pulmonary lesions during active disease. In order to compare the NK cell ability to react to free mycobacteria in the context of tuberculosis infection and Mycobacterium bovis BCG vaccination, NK cells were isolated from the peripheral blood of anonymous healthy human donors, and stimulated with M. tuberculosis H37Rv or M. bovis BCG. Extracellular M. tuberculosis and M. bovis BCG could equally trigger the release of IFNγ and TNFα from NK cells in the presence of IL-2. However, we found that this response varied 1000-fold between individuals (n = 52), with differences in KIR haplotype providing a significant criterion to distinguish between low and high responders. Our findings suggest that variations at the KIR locus and therefore of the NK cell repertoire may affect cytokine production in response to mycobacteria and we propose that this innate variability couldsustain different levels of susceptibility to M. tuberculosis infection.

Indexed as

HaplotypesDisease SusceptibilityHumansInterferon-gammaInterleukin-2Killer Cells, NaturalMycobacterium bovisMycobacterium tuberculosisReceptors, KIRTuberculosis, PulmonaryTumor Necrosis Factor-alphaInterferon-gammaInterleukin-2Receptors, KIRTumor Necrosis Factor-alpha

Identifiers

PMID22788220
PMCPMC3503254
OpenAlexW1569643796

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.