Evidence map›Paper›PMID 18246079›Full record

ArticleNature medicine2008

Mouse models of rhinovirus-induced disease and exacerbation of allergic airway inflammation.

Nathan W Bartlett, Ross P Walton, Michael R Edwards, Juliya Aniscenko, Gaetano Caramori, Jie Zhu, Nicholas Glanville, Katherine J Choy, Patrick Jourdan, Jerome Burnet and 18 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Nature medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05775952 (Comparison of Airway Remodeling Mediators Following Experimental Human Rhinovirus Infection in Subjects With Mild to Moderate Asthma and Healthy, Non-asthmatic Control Subjects), which is not on this map. Cited by 199 papers.

0numbers the graph read from it
0cells of the map it votes in
199citing papers in PubMed
16.8field-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.

NCT05775952 unknown statusnot on this mapstarted 2011, after this paper: background citation

Comparison of Airway Remodeling Mediators Following Experimental Human Rhinovirus Infection in Subjects With Mild to Moderate Asthma and Healthy, Non-asthmatic Control Subjects

TypeobservationalSponsorUniversity of CalgaryRan2011 to 2024Enrolled24ConditionsAsthma, Respiratory DiseaseArmsHRV-39
3 · Its place in the literature

Who cites it

199 citing papers in PubMed, 372 citations in OpenAlex.

  1. Rhinovirus-induced CCL17 and CCL22 in Asthma Exacerbations and Differential Regulation by STAT6.American journal of respiratory cell and molecular biology · 2021
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  18. Targeting respiratory virus-induced reactive oxygen species in airways diseases.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
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  20. Article

139 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

28 authors at 10 institutions in 4 countries.

Nathan W BartlettDepartment of Respiratory Medicine, UK National Heart and Lung Institute, and Medical Research Council & Asthma UK Centre in Allergic Mechanisms of Asthma, Imperial College London, Norfolk Place, London W2 1PG, UK.
Ross P Walton
Michael R Edwards
Juliya Aniscenko
Gaetano Caramori
Jie Zhu
Nicholas Glanville
Katherine J Choy
Patrick Jourdan
Jerome Burnet
Tobias J Tuthill
Michael S Pedrick
Michael J Hurle
Chris Plumpton
Nigel A Sharp
James N Bussell
Dallas M Swallow
Jurgen Schwarze
Bruno Guy
Jeffrey W Almond
Peter K Jeffery
Clare M Lloyd
Alberto Papi
Richard A Killington
David J Rowlands
Edward D Blair
Neil J Clarke
Sebastian L Johnston
Age UK · GBImperial College London · GBMedical Research Council · GBUniversity of Leeds · GBAsthma UK · GBGlaxoSmithKline (United Kingdom) · GBNational Institutes of Health · USSanofi (France) · FRUniversity of Ferrara · ITUniversity College London · GB

Funding

Wellcome Trust 057704Wellcome Trust 087618
6 · The paper itself

Abstract

Rhinoviruses cause serious morbidity and mortality as the major etiological agents of asthma exacerbations and the common cold. A major obstacle to understanding disease pathogenesis and to the development of effective therapies has been the lack of a small-animal model for rhinovirus infection. Of the 100 known rhinovirus serotypes, 90% (the major group) use human intercellular adhesion molecule-1 (ICAM-1) as their cellular receptor and do not bind mouse ICAM-1; the remaining 10% (the minor group) use a member of the low-density lipoprotein receptor family and can bind the mouse counterpart. Here we describe three novel mouse models of rhinovirus infection: minor-group rhinovirus infection of BALB/c mice, major-group rhinovirus infection of transgenic BALB/c mice expressing a mouse-human ICAM-1 chimera and rhinovirus-induced exacerbation of allergic airway inflammation. These models have features similar to those observed in rhinovirus infection in humans, including augmentation of allergic airway inflammation, and will be useful in the development of future therapies for colds and asthma exacerbations.

Indexed as

Disease Models, AnimalAnimalsAntibody FormationBronchial HyperreactivityChemokinesChemotactic FactorsDendritic CellsHumansHypersensitivityImmunity, InnateInflammationInflammation MediatorsIntercellular Adhesion Molecule-1MiceMice, TransgenicMucusChemokinesChemotactic FactorsInflammation MediatorsIntercellular Adhesion Molecule-1

Identifiers

PMID18246079
PMCPMC3384678
OpenAlexW2065220920

What OpenQuestion holds

Textmetadata
LicenceTDM
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.