Evidence map›Paper›PMID 9177232›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

A chemoattractant cytokine associated with granulomas in tuberculosis and silicosis.

G J Nau, P Guilfoile, G L Chupp, J S Berman, S J Kim, H Kornfeld, R A Young

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
7.0field-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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 191 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. The Role of Osteopontin in Respiratory Health and Disease.Journal of personalized medicine · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Transcriptomics in toxicology.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2017
    Review
  17. Article
  18. Article
  19. Article
  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

7 authors at 3 institutions in 1 country.

G J NauWhitehead Institute for Biomedical Research, Nine Cambridge Center, and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
P Guilfoile
G L Chupp
J S Berman
S J Kim
H Kornfeld
R A Young
Boston University · USMassachusetts Institute of Technology · USWhitehead Institute for Biomedical Research · US

Funding

MONOCLONAL ANTIBODIES FOR DEVELOPMENTAL STUDIESN01HD062915 · NICHD · JOHNS HOPKINS UNIVERSITY · PI AUGUST, J THOMAS · 1986 to 1991
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MACROPHAGE AND MYCOBACTERIA--GENES AND GENOMESR01AI037869 · NIAID · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI YOUNG, RICHARD A · 1995 to 1999
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ANTIMICROBIAL FUNCTION HIV-INFECTED ALVEOLAR MACROPHAGESR01HL044846 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KORNFELD, HARDY · 1990 to 1999
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NHLBI NIH HHS HL44846NIAID NIH HHS AI 37869NICHD NIH HHS N01-HD-6-2915
6 · The paper itself

Abstract

Chronic inflammation and granuloma formation are associated with mononuclear cell infiltrates and are characteristic pathologic responses in tuberculosis. To identify host cell genes involved in tuberculous pathology, we screened macrophage cDNA libraries for genes induced by mycobacterial infection. One gene isolated in this screen, osteopontin (also known as early T lymphocyte activation protein 1 or Eta-1), was of particular interest because it is a cytokine and macrophage chemoattractant. Further study revealed that Mycobacterium tuberculosis infection of primary human alveolar macrophages causes a substantial increase in osteopontin gene expression. Osteopontin protein was identified by immunohistochemistry in macrophages, lymphocytes, and the extracellular matrix of pathologic tissue sections of patients with tuberculosis. Increased osteopontin expression also was found to be associated with silicosis, another granulomatous disease. The association of osteopontin with granulomatous pathology, together with the known properties of the protein, suggest that osteopontin may participate in granuloma formation. The strategy of identifying host genes whose expression is altered by infection thus can provide valuable clues to disease mechanisms and will be increasingly valuable as additional human genome sequences become available.

Indexed as

BronchopneumoniaCell LineChemokine CCL4Chemotactic FactorsCytokinesDNA PrimersFerritinsGene LibraryGranulomaHumansImmunohistochemistryMacrophage Inflammatory ProteinsMacrophagesMacrophages, AlveolarMycobacterium bovisMycobacterium tuberculosisChemokine CCL4Chemotactic FactorsCytokinesDNA PrimersFerritinsMacrophage Inflammatory ProteinsOsteopontinSialoglycoproteinsSPP1 protein, human

Identifiers

PMID9177232
PMCPMC21064
OpenAlexW2137801669

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.