Evidence map›Paper›PMID 11179353›Full record

ArticleInfection and immunity2001

Human natural killer cells mediate killing of intracellular Mycobacterium tuberculosis H37Rv via granule-independent mechanisms.

K J Brill, Q Li, R Larkin, D H Canaday, D R Kaplan, W H Boom, R F Silver

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Tuberculosis treatment and cytotoxic immune signatures: a longitudinal study.Journal of clinical tuberculosis and other mycobacterial diseases · 2026
    Article
  4. Review
  5. Review
  6. Mixed infections and heteroresistance ofEmerging microbes & infections · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Distinct Human NK Cell Phenotypes and Functional Responses toFrontiers in cellular and infection microbiology · 2020
    Article
  18. Review
  19. Review
  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

7 authors at 4 institutions in 1 country.

K J BrillDivisions of Pulmonary and Critical Care Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
Q Li
R Larkin
D H Canaday
D R Kaplan
W H Boom
R F Silver
Pulmonary and Critical Care Associates · USUniversity Hospitals of Cleveland · USCase Western Reserve University · USOffice of Infectious Diseases · US

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI John Christian Tilton · 1994 to 2026
$50.0M
Tuberculosis Prevention Research Unit /TBRU/-266095383N01AI095383 · NIAID · CASE WESTERN RESERVE UNIVERSITY · 2000 to 2005
$5.6M
HETEROGENEITY OF TCELLS IN M TUBERCULOSIS INFECTIONR01AI027243 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY · 1989 to 2016
$5.5M
CD8+ T CELLS AND MYCOPLASMA TUBERCULOSISK08AI001581 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI CANADAY, DAVID H · 1999 to 2003
$471k
SECOND-GENERATION VACCINES AGAINST LYME DISEASER01AI035027 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI PHILIPP, MARIO TOMAS · 1994 to 1996
–
SECOND GENERATION VACCINES AGAINST LYME DISEASER21AI035027 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI PHILIPP, MARIO TOMAS · 1998 to 1998
–
NHLBI NIH HHS HL59851NIAID NIH HHS AI01581NIAID NIH HHS AI27243NIAID NIH HHS AI35027NIAID NIH HHS AI36219NIAID NIH HHS K08 AI001581NIAID NIH HHS N01 AI095383NIAID NIH HHS P30 AI036219NIAID NIH HHS R01 AI027243
6 · The paper itself

Abstract

Despite the continued importance of tuberculosis as a world-wide threat to public health, little is known about the mechanisms used by human lymphocytes to contain and kill the intracellular pathogen Mycobacterium tuberculosis. We previously described an in vitro model of infection of human monocytes (MN) with virulent M. tuberculosis strain H37Rv in which the ability of peripheral blood lymphocytes to limit intracellular growth of the organism could be measured. In the current study, we determined that lymphocyte-mediated killing of intracellular M. tuberculosis occurs within the first 24 h of coculture with infected MN. Natural killer (NK) cells isolated from both purified protein derivative (PPD)-positive and PPD-negative subjects were capable of mediating this early killing of intracellular H37Rv. NK cell-mediated killing of intracellular M. tuberculosis was not associated with the production of gamma interferon. Transferred supernatants of cocultured NK cells and M. tuberculosis-infected MN could not mediate the killing of intracellular M. tuberculosis, and Transwell studies indicated that direct cell-to-cell contact was required for NK cells to mediate the killing of the organism. Killing was not dependent upon exocytosis of NK cell cytotoxic granules. NK cells induced apoptosis of mycobacterium-infected MN, but neither killing of intracellular M. tuberculosis by NK cells nor NK cell-induced apoptosis of infected MN was inhibited by blocking the interaction of FasL and Fas. Thus, human NK cells may mediate killing of intracellular M. tuberculosis via alternative apoptotic pathways.

Indexed as

ApoptosisAdultCell CommunicationCoculture TechniquesCytoplasmic GranulesFas Ligand Proteinfas ReceptorHumansInterferon-gammaKiller Cells, NaturalLymphocytesMembrane GlycoproteinsMiddle AgedMycobacterium bovisMycobacterium tuberculosisFASLG protein, humanFas Ligand Proteinfas ReceptorInterferon-gammaMembrane Glycoproteins

Identifiers

PMID11179353
PMCPMC98082
OpenAlexW2149051564

What OpenQuestion holds

Textmetadata
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.