Evidence map›Paper›PMID 16352737›Full record

ArticleThe Journal of experimental medicine2005

A functional promoter polymorphism in monocyte chemoattractant protein-1 is associated with increased susceptibility to pulmonary tuberculosis.

Pedro O Flores-Villanueva, Jorge A Ruiz-Morales, Chang-Hwa Song, Ludmila M Flores, Eun-Kyeong Jo, Marta Montaño, Peter F Barnes, Moises Selman, Julio Granados

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 3 pooled it
8.3field-weighted citation impact, top 2% 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

106 citing papers in PubMed, 3 syntheses or guidelines pooled it, 238 citations in OpenAlex.

  1. Pooled it
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  4. Trial
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  7. Article
  8. Single nucleotide variants in theFrontiers in cellular and infection microbiology · 2024
    Observational
  9. Review
  10. Review
  11. Article
  12. CC Chemokine Receptor 4 (CCR4) as a Possible New Target for Therapy.International journal of molecular sciences · 2022
    Review
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  14. Article
  15. Article
  16. Article
  17. Article
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46 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Pedro O Flores-VillanuevaCenter for Biomedical Research, University of Texas Health Center at Tyler, Tyler, TX 75708, USA. pedro.flores@UTHCT.edu
Jorge A Ruiz-Morales
Chang-Hwa Song
Ludmila M Flores
Eun-Kyeong Jo
Marta Montaño
Peter F Barnes
Moises Selman
Julio Granados
The University of Texas Health Science Center at Tyler · USChungnam National University · KRDana-Farber Cancer Institute · US

Funding

SCHOLARS IN CLINICAL SCIENCE PROGRAMK30HL004095 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WILLIAMS, GORDON H · 1999 to 2004
$1.0M
MCP-1 and susceptibility to active tuberculosisR21HL072177 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI FLORES-VILLANUEVA, PEDRO OMAR · 2002 to 2003
$472k
NHLBI NIH HHS HL04095-04NHLBI NIH HHS K30 HL004095NHLBI NIH HHS R21 HL072177NHLBI NIH HHS R21 HL72177
6 · The paper itself

Abstract

We examined the distribution of single nucleotide polymorphisms (SNPs) in nitric oxide synthase 2A, monocyte chemoattractant protein-1 (MCP-1), regulated on activation, normal T cell expressed and secreted, and macrophage inflammatory protein-1alpha genes in tuberculosis patients and healthy controls from Mexico. The odds of developing tuberculosis were 2.3- and 5.4-fold higher in carriers of MCP-1 genotypes AG and GG than in homozygous AA. Cases of homozygous GG had the highest plasma levels of MCP-1 and the lowest plasma levels of IL-12p40, and these values were negatively correlated. Furthermore, stimulation of monocytes from healthy carriers of the genotype GG with Mycobacterium tuberculosis antigens yielded higher MCP-1 and lower IL-12p40 concentrations than parallel experiments with monocytes from homozygous AA. Addition of anti-MCP-1 increased IL-12p40 levels in cultures of M. tuberculosis-stimulated monocytes from homozygous GG, and addition of exogenous MCP-1 reduced IL-12p40 production by M. tuberculosis-stimulated monocytes from homozygous AA. Furthermore, we could replicate our results in Korean subjects, in whom the odds of developing tuberculosis were 2.8- and 6.9-fold higher in carriers of MCP-1 genotypes AG and GG than in homozygous AA. Our findings suggest that persons bearing the MCP-1 genotype GG produce high concentrations of MCP-1, which inhibits production of IL-12p40 in response to M. tuberculosis and increases the likelihood that M. tuberculosis infection will progress to active pulmonary tuberculosis.

Indexed as

Epistasis, GeneticGenetic Predisposition to DiseaseAdultAgedChemokine CCL2Chemokine CCL4DNA PrimersEnzyme-Linked Immunosorbent AssayHumansInterleukin-12Interleukin-12 Subunit p40KoreaMacrophage Inflammatory ProteinsMexicoMiddle AgedNitric Oxide Synthase Type IICCL2 protein, humanChemokine CCL2Chemokine CCL4DNA PrimersInterleukin-12Interleukin-12 Subunit p40Macrophage Inflammatory ProteinsNitric Oxide Synthase Type IINOS2 protein, humanProtein Subunits

Identifiers

PMID16352737
PMCPMC2212957
OpenAlexW2127513692

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.