Evidence map›Paper›PMID 23935498›Full record

ArticlePLoS pathogens2013

An anti-human ICAM-1 antibody inhibits rhinovirus-induced exacerbations of lung inflammation.

Stephanie Traub, Alexandra Nikonova, Alan Carruthers, Rebecca Dunmore, Katherine A Vousden, Leila Gogsadze, Weidong Hao, Qing Zhu, Katie Bernard, Jie Zhu and 12 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. 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
4.4field-weighted citation impact, top 5% 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, 71 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
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  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. A Pandemic Lesson for Global Lung Diseases: Exacerbations Are Preventable.American journal of respiratory and critical care medicine · 2022
    Review
  11. Review
  12. Role of air pollutants in airway epithelial barrier dysfunction in asthma and COPD.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  13. Article
  14. Rhinovirus and asthma: Challenges and opportunities.Reviews in medical virology · 2021
    Review
  15. Article
  16. Review
  17. Review
  18. Smoking and COVID-19: What we know so far.Respiratory medicine · 2021
    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

22 authors at 5 institutions in 2 countries.

Stephanie TraubNational Heart and Lung Institute, MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, Centre for Respiratory Infection, Imperial College London, London, United Kingdom.
Alexandra Nikonova
Alan Carruthers
Rebecca Dunmore
Katherine A Vousden
Leila Gogsadze
Weidong Hao
Qing Zhu
Katie Bernard
Jie Zhu
Michael Dymond
Gary R McLean
Ross P Walton
Nicholas Glanville
Alison Humbles
Musa Khaitov
Ted Wells
Roland Kolbeck
Andrew J Leishman
Matthew A Sleeman
Nathan W Bartlett
Sebastian L Johnston
Imperial College London · GBAimmune Therapeutics (United Kingdom) · GBAsthma UK · GBAstraZeneca (United Kingdom) · GBInstitute of Immunology and Physiology · RU

Funding

Medical Research Council G1000758Medical Research Council G1100168Wellcome Trust
6 · The paper itself

Abstract

Human rhinoviruses (HRV) cause the majority of common colds and acute exacerbations of asthma and chronic obstructive pulmonary disease (COPD). Effective therapies are urgently needed, but no licensed treatments or vaccines currently exist. Of the 100 identified serotypes, ∼90% bind domain 1 of human intercellular adhesion molecule-1 (ICAM-1) as their cellular receptor, making this an attractive target for development of therapies; however, ICAM-1 domain 1 is also required for host defence and regulation of cell trafficking, principally via its major ligand LFA-1. Using a mouse anti-human ICAM-1 antibody (14C11) that specifically binds domain 1 of human ICAM-1, we show that 14C11 administered topically or systemically prevented entry of two major groups of rhinoviruses, HRV16 and HRV14, and reduced cellular inflammation, pro-inflammatory cytokine induction and virus load in vivo. 14C11 also reduced cellular inflammation and Th2 cytokine/chemokine production in a model of major group HRV-induced asthma exacerbation. Interestingly, 14C11 did not prevent cell adhesion via human ICAM-1/LFA-1 interactions in vitro, suggesting the epitope targeted by 14C11 was specific for viral entry. Thus a human ICAM-1 domain-1-specific antibody can prevent major group HRV entry and induction of airway inflammation in vivo.

Indexed as

AnimalsAntibodies, Monoclonal, Murine-DerivedChemokinesHeLa CellsHumansImmunoglobulin GIntercellular Adhesion Molecule-1Jurkat CellsLymphocyte Function-Associated Antigen-1MiceMice, TransgenicPicornaviridae InfectionsPneumonia, ViralRhinovirusTh2 CellsVirus InternalizationAntibodies, Monoclonal, Murine-DerivedChemokinesImmunoglobulin GIntercellular Adhesion Molecule-1Lymphocyte Function-Associated Antigen-1

Identifiers

PMID23935498
PMCPMC3731244
OpenAlexW2040248326

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.