Evidence map›Paper›PMID 8514874›Full record

ArticleThe Journal of clinical investigation1993

Human eosinophils can express the cytokines tumor necrosis factor-alpha and macrophage inflammatory protein-1 alpha.

J J Costa, K Matossian, M B Resnick, W J Beil, D T Wong, J R Gordon, A M Dvorak, P F Weller, S J Galli

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
19.3field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 187 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. An update on the diagnostic biomarkers for asthma.Journal of family medicine and primary care · 2021
    Review
  5. Article
  6. DisruptingMicroorganisms · 2020
    Article
  7. Review
  8. Review
  9. Liquiritin apioside attenuates laryngeal chemoreflex but not mechanoreflex in rat pups.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
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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 2 institutions in 2 countries.

J J CostaDepartment of Pathology, Beth Israel Hospital, Boston, Massachusetts 02215.
K Matossian
M B Resnick
W J Beil
D T Wong
J R Gordon
A M Dvorak
P F Weller
S J Galli
University of Saskatchewan · CABrigham and Women's Hospital · US

Funding

Regulation of Mast Cell Development and FunctionR01AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1986 to 2010
$2.4M
REGULATION OF MAST CELL DEVELOPMENT &FUNCTIONR37AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN J · 1996 to 2005
$2.2M
ROLE OF MAST CELLS IN INFLAMMATION AND IMMUNITYR01AI022674 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GALLI, STEPHEN J · 1986 to 1995
–
MAST CELL &EOSINOPHIL CYTOKINES IN ALLERGIC DISORDERSR01AI031982 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GALLI, STEPHEN J · 1992 to 1994
–
NIAID NIH HHS AI22674NIAID NIH HHS AI23990NIAID NIH HHS AI31982
6 · The paper itself

Abstract

By in situ hybridization, 44-100% of the blood eosinophils from five patients with hypereosinophilia and four normal subjects exhibited intense hybridization signals for TNF-alpha mRNA. TNF-alpha protein was detectable by immunohistochemistry in blood eosinophils of hypereosinophilic subjects, and purified blood eosinophils from three atopic donors exhibited cycloheximide-inhibitable spontaneous release of TNF-alpha in vitro. Many blood eosinophils (39-91%) from hypereosinophilic donors exhibited intense labeling for macrophage inflammatory protein-1 alpha (MIP-1 alpha) mRNA, whereas eosinophils of normal donors demonstrated only weak or undetectable hybridization signals for MIP-1 alpha mRNA. Most tissue eosinophils infiltrating nasal polyps were strongly positive for both TNF-alpha and MIP-1 alpha mRNA. By Northern blot analysis, highly enriched blood eosinophils from a patient with the idiopathic hypereosinophilic syndrome exhibited differential expression of TNF-alpha and MIP-1 alpha mRNA. These findings indicate that human eosinophils represent a potential source of TNF-alpha and MIP-1 alpha, that levels of expression of mRNA for both cytokines are high in the blood eosinophils of hypereosinophilic donors and in eosinophils infiltrating nasal polyps, that the eosinophils of normal subjects express higher levels of TNF-alpha than MIP-1 alpha mRNA, and that eosinophils purified from the blood of atopic donors can release TNF-alpha in vitro.

Indexed as

Cells, CulturedChemokine CCL4CytokinesEosinophiliaEosinophilsHumansImmunohistochemistryIn Situ HybridizationMacrophage Inflammatory ProteinsMaleMonokinesRNA, MessengerTumor Necrosis Factor-alphaChemokine CCL4CytokinesMacrophage Inflammatory ProteinsMonokinesRNA, MessengerTumor Necrosis Factor-alpha

Identifiers

PMID8514874
PMCPMC443331
OpenAlexW2038273933

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.