Evidence map›Paper›PMID 9312163›Full record

ArticleThe Journal of clinical investigation1997

Chemokine-induced eosinophil recruitment. Evidence of a role for endogenous eotaxin in an in vivo allergy model in mouse skin.

M M Teixeira, T N Wells, N W Lukacs, A E Proudfoot, S L Kunkel, T J Williams, P G Hellewell

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
10.0field-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

43 citing papers in PubMed, 170 citations in OpenAlex.

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  13. Dietary ω-3 fatty acids alter the lipid mediator profile and alleviate allergic conjunctivitis without modulating TFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  14. Review
  15. Article
  16. Roles and regulation of gastrointestinal eosinophils in immunity and disease.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Review
  17. Article
  18. IgE, mast cells, and eosinophils in atopic dermatitis.Clinical reviews in allergy & immunology · 2011
    Review
  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 2 countries.

M M TeixeiraApplied Pharmacology, Imperial College School of Medicine at the National Heart and Lung Institute, London, SW3 6LY, United Kingdom. mauro.teixeira@ic.ac.uk
T N Wells
N W Lukacs
A E Proudfoot
S L Kunkel
T J Williams
P G Hellewell
Imperial College London · GBBiomedical Research Institute · USUniversity of Michigan–Ann Arbor · US

Funding

The Role of C-C Chemokines in Eosinophil Airway InflammationR01AI036302 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKACS, NICHOLAS W · 2001 to 2018
$5.6M
MONOCYTE/MACROPHAGE SIGNALS IN LUNG GRANULOMAR37HL035276 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KUNKEL, STEVEN LYNN · 1996 to 2005
$1.4M
C-C CHEMOKINES AND EOSINOPHIL AIRWAY INFLAMMATIONR29AI036302 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKACS, NICHOLAS W · 1996 to 2000
$107k
MONOCYTE/MACROPHAGE SIGNALS IN LUNG GRANULOMAR01HL035276 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KUNKEL, STEVEN LYNN · 1987 to 1996
–
NHLBI NIH HHS HL35276NIAID NIH HHS AI36302Wellcome Trust
6 · The paper itself

Abstract

Selective eosinophil recruitment into tissues is a characteristic feature of allergic diseases. Chemokines are effective leukocyte chemoattractants and may play an important role in mediating eosinophil recruitment in various allergic conditions in man. Here, we describe a novel mouse model of eosinophil recruitment in which we have compared the in vivo chemoattractant activity of different C-C chemokines. Furthermore, we describe the use of antibodies to chemokines and receptor blockade to address the endogenous mechanisms involved in eosinophil recruitment in a late-phase allergic reaction in mouse skin. Intradermal injection of mEotaxin and mMIP-1alpha, but not mMCP-1, mRANTES, mMCP-5, or mMIP-1beta, induced significant 111In-eosinophil recruitment in mouse skin. Significant 111In-eosinophil recruitment was also observed in an active cutaneous anaphylactic reaction. Pretreatment of skin sites with antieotaxin antiserum, but not an antiMIP-1alpha antibody, suppressed 111In-eosinophil recruitment in this delayed-onset allergic reaction. Similarly, desensitization of the eosinophil eotaxin receptor CCR3 with mEotaxin, or blockade of the receptor with metRANTES, significantly inhibited 111In-eosinophil recruitment in the allergic reaction. These results demonstrate an important role for endogenous eotaxin in mediating the 111In-eosinophil recruitment in allergic inflammation, and suggest that blockade of the CCR3 receptor is a valid strategy to inhibit eosinophil migration in vivo.

Indexed as

Chemotaxis, LeukocyteAnaphylaxisAnimalsChemokine CCL11Chemokines, CCChemotactic Factors, EosinophilComplement C5aCytokinesEosinophilsFemaleHypersensitivityHypersensitivity, DelayedLeukotriene B4MiceMice, Inbred CBAPlatelet Activating FactorCcl11 protein, mouseCcr3 protein, mouseChemokine CCL11Chemokines, CCChemotactic Factors, EosinophilComplement C5aCytokinesLeukotriene B4Platelet Activating FactorReceptors, CCR3Receptors, Chemokine

Identifiers

PMID9312163
PMCPMC508348
OpenAlexW2039980834

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.