Evidence map›Paper›PMID 24190334›Full record

ArticlePathogens and disease2014

Inhibition of toll-like receptor 2 (TLR-2)-mediated response in human alveolar epithelial cells by mycolic acids and Mycobacterium tuberculosis mce1 operon mutant.

Patricia C Sequeira, Ryan H Senaratne, Lee W Riley

Open access · bronzeAbstract read
In one paragraph

Article in Pathogens and disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Significance of genotypes and resistance status ofIranian journal of basic medical sciences · 2024
    Article
  3. Review
  4. Review
  5. Journal of thoracic disease · 2023
    Article
  6. Dual RNA Sequencing ofInternational journal of molecular sciences · 2022
    Article
  7. Review
  8. Article
  9. TLR-9 Plays a Role inFrontiers in immunology · 2021
    Article
  10. Evolution of Drug-ResistantFrontiers in microbiology · 2021
    Review
  11. The Journal of biological chemistry · 2020
    Article
  12. Article
  13. Underestimated Manipulative Roles ofFrontiers in immunology · 2019
    Review
  14. Review
  15. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2018
    Review
  16. Review
  17. 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

3 authors at 1 institution in 1 country.

Patricia C SequeiraSchool of Public Health, University of California, Berkeley, CA, USA.
Ryan H Senaratne
Lee W Riley
University of California, Berkeley · US

Funding

MOLECULAR BIOLOGY OF INFECTION WITH M TUBERCULOSISR01AI035266 · NIAID · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI RILEY, LEE W · 1993 to 2002
$781k
NIAID NIH HHS R01 AI035266NIAID NIH HHS R01AI035266
6 · The paper itself

Abstract

In human lungs, the earliest encounter of Mycobacterium tuberculosis, the agent of tuberculosis, involves alveolar epithelial cells. Droplets expectorated by a patient with tuberculosis are likely to contain a mixed population of M. tuberculosis cells in different physiologic and metabolic states from the lung lesions of the patient. Here, we compared the chemokine expression patterns of human epithelial cell line A549 and RAW 264.7 macrophage cells infected with wild-type M. tuberculosis H37Rv against patterns induced by a mutant that accumulates free mycolic acids in its cell wall (Δmce1). We also examined the effect of free mycolic acids on toll-like receptor-2 (TLR-2). Wild-type M. tuberculosis induced significantly higher levels of IL-8, MCP-1, RANTES, and IP-10 in both cell types than did Δmce. Free mycolic acids reduced the ability of the mammalian cells to respond to a TLR-2 agonist in a dose-dependent manner. These observations suggest that differences in mycolic acid abundance in the M. tuberculosis cell wall can affect TLR-2-mediated pro-inflammatory response in both epithelial and macrophage cells. The final fate of a new infection may be ultimately determined by the proportion of M. tuberculosis cells expressing free mycolates in the infecting inoculum population.

Indexed as

AnimalsBacterial ProteinsCell LineEpithelial CellsHumansImmunosuppressive AgentsMacrophagesMutationMycobacterium tuberculosisMycolic AcidsToll-Like Receptor 2Bacterial ProteinsImmunosuppressive Agentsmammalian cell entry protein Mce1A, Mycobacterium tuberculosisMycolic AcidsToll-Like Receptor 2A549 cellsalveolar epithelial cellsmce1 operonMycobacterium tuberculosismycolic acidtuberculosis

Identifiers

PMID24190334
PMCPMC6433132
OpenAlexW2091804922

What OpenQuestion holds

Textmetadata
LicenceTDM
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.