Evidence map›Paper›PMID 9221761›Full record

ArticleThe Journal of experimental medicine1997

Human peripheral blood eosinophils express a functional c-kit receptor for stem cell factor that stimulates very late antigen 4 (VLA-4)-mediated cell adhesion to fibronectin and vascular cell adhesion molecule 1 (VCAM-1).

Q Yuan, K F Austen, D S Friend, M Heidtman, J A Boyce

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01097694 (A 28 Week, Treatment Randomized, Double -Blind, Placebo-controlled Study of the Effects of cKit Inhibition by Imatinib in Patients With Severe Refractory Asthma), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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.

NCT01097694 phase2completednot on this mapstarted 2010, after this paper: background citation

A 28 Week, Treatment Randomized, Double -Blind, Placebo-controlled Study of the Effects of cKit Inhibition by Imatinib in Patients With Severe Refractory Asthma (KIA)

TypeinterventionalSponsorBrigham and Women's HospitalRan2010 to 2016Enrolled176ConditionsAsthmaArmsImatinib mesylate, Placebo
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. KIT as a master regulator of the mast cell lineage.The Journal of allergy and clinical immunology · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Intranasal sirna targeting c-kit reduces airway inflammation in experimental allergic asthma.International journal of clinical and experimental pathology · 2014
    Article
  13. Article
  14. Review
  15. Endothelial-mesenchymal transition in bleomycin-induced pulmonary fibrosis.American journal of respiratory cell and molecular biology · 2010
    Article
  16. Hypoxia modulates human eosinophil function.Clinical and molecular allergy : CMA · 2010
    Article
  17. FIP1L1/PDGFR alpha-associated systemic mastocytosis.International archives of allergy and immunology · 2010
    Review
  18. Expression of ADAMs ("a disintegrin and metalloprotease") in the human lung.Virchows Archiv : an international journal of pathology · 2009
    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

5 authors at 2 institutions in 1 country.

Q YuanDepartment of Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA.
K F Austen
D S Friend
M Heidtman
J A Boyce
Harvard University · USBrigham and Women's Hospital · US

Funding

Role of PGE2 in Human Mast Cell BiologyP01HL036110 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI BEIER, DAVID R. · 1985 to 2009
$20.1M
Role of Integrin alphaEbeta7 on Th2 Immune ResponsesP01AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, KARL FRANK · 1999 to 2007
$7.7M
IN VITRO STUDIES OF THE MECHANISM OF ANAPHYLAXISR01AI022531 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, K. FRANK · 1985 to 1989
–
IN VITRO STUDIES OF THE MECHANISM OF ANAPHYLAXISR37AI022531 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, K. FRANK · 1990 to 1999
–
URINARY AND EXCRETION OF LTR AS AN INDEX OF AIRWAY RESPONSESU01AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI DRAZEN, JEFFREY M · 1991 to 1994
–
THE V3 MASTOCYTOSIS MOUSE--MAST CELL DIFFERENTIATION, MATURATION, AND FUNCTIONU19AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, K. FRANK · 1995 to 1998
–
NHLBI NIH HHS P01 HL036110NIAID NIH HHS AI-01304NIAID NIH HHS AI-22531NIAID NIH HHS AI-31599NIAID NIH HHS P01 AI031599NIAID NIH HHS U19 AI031599
6 · The paper itself

Abstract

We evaluated mature peripheral blood eosinophils for their expression of the surface tyrosine kinase, c-kit, the receptor for the stromal cell-derived cytokine, stem cell factor (SCF). Cytofluorographic analysis revealed that c-kit was expressed on the purified peripheral blood eosinophils from 8 of 8 donors (4 nonatopic and 4 atopic) (mean channel fluorescence intensity 2.0- 3. 6-fold, average 2.8 +/- 0.6-fold, greater than the negative control). The uniform and selective expression of c-kit by eosinophils was confirmed by immunohistochemical analysis of peripheral blood buffy coats. The functional integrity of c-kit was demonstrated by the capacity of 100 ng/ml (5 nM) of recombinant human (rh) SCF to increase eosinophil adhesion to 3, 10, and 30 microg/ml of immobilized FN40, a 40-kD chymotryptic fragment of plasma fibronectin, in 15 min by 7.7 +/- 1.4-, 5.3 +/- 3.3-, and 5.4 +/- 0. 2-fold, respectively, and their adhesion to 0.1, 0.5, and 1.0 microg/ml vascular cell adhesion molecule-1 (VCAM-1), by 12.7 +/- 9. 2-, 3.8 +/- 2.5-, and 1.7 +/- 0.6-fold, respectively. The SCF-stimulated adhesion occurred without concomitant changes in surface integrin expression, thereby indicating an avidity-based mechanism. rhSCF (100 ng/ml, 5 nM) was comparable to rh eotaxin (200 ng/ml, 24 nM) in stimulating adhesion. Cell adhesion to FN40 was completely inhibited with antibodies against the alpha4 and beta1 integrin subunits, revealing that the SCF/c-kit adhesion effect was mediated by a single integrin heterodimer, very late antigen 4 (VLA-4). Thus, SCF represents a newly recognized stromal ligand for the activation of eosinophils for VLA-4-mediated adhesion, which could contribute to the exit of these cells from the blood, their tissue localization, and their prominence in inflammatory lesions.

Indexed as

Chemokines, CCCell AdhesionChemokine CCL11CytokinesEosinophilsFibronectinsHumansImmunohistochemistryIntegrin alpha4beta1IntegrinsProto-Oncogene Proteins c-kitReceptors, Lymphocyte HomingRecombinant ProteinsStem Cell FactorVascular Cell Adhesion Molecule-1CCL11 protein, humanChemokine CCL11Chemokines, CCCytokinesFibronectinsIntegrin alpha4beta1IntegrinsProto-Oncogene Proteins c-kitReceptors, Lymphocyte HomingRecombinant ProteinsStem Cell FactorVascular Cell Adhesion Molecule-1

Identifiers

PMID9221761
PMCPMC2198988
OpenAlexW2104648805

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.