Evidence map›Paper›PMID 24348661›Full record

ArticleKorean journal of pediatrics2013

The effect of rhinovirus on airway inflammation in a murine asthma model.

Eugene Kim, Huisu Lee, Hyun Sook Kim, Sulmui Won, Eu Kyoung Lee, Hwan Soo Kim, Kyongwon Bang, Yoon Hong Chun, Jong-Seo Yoon, Hyun Hee Kim and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Korean journal of pediatrics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Viruses and non-allergen environmental triggers in asthma.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2019
    Review
  2. Article
  3. Review
  4. Reply.The Journal of allergy and clinical immunology · 2017
    Article
  5. 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

12 authors at 1 institution in 1 country.

Eugene KimDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Huisu LeeDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Hyun Sook KimDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Sulmui WonDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Eu Kyoung LeeDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Hwan Soo KimDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Kyongwon BangDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Yoon Hong ChunDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Jong-Seo YoonDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Hyun Hee KimDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Jin Tack KimDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Joon Sung LeeDepartment of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.
Catholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of the present study was to investigate the differences in lower airway inflammatory immune responses, including cellular responses and responses in terms of inflammatory mediators in bronchoalveolar lavage fluid (BALF) and the airway, to rhinovirus (RV) infection on asthma exacerbation by comparing a control and a murine asthma model, with or without RV infection.

methodsBALB/c mice were intraperitoneally injected with a crude extract of Dermatophagoides farinae (Df) or phosphate buffered saline (PBS) and were subsequently intranasally treated with a crude extract of Df or PBS. Airway responsiveness and cell infiltration, differential cell counts in BALF, and cytokine and chemokine concentrations in BALF were measured 24 hours after intranasal RV1B infection.

resultsRV infection increased the enhanced pause (Penh) in both the Df sensitized and challenged mice (Df mice) and PBS-treated mice (PBS mice) (P<0.05). Airway eosinophil infiltration increased in Df mice after RV infection (P<0.05). The levels of interleukin (IL) 13, tumor necrosis factor alpha, and regulated on activation, normal T cells expressed and secreted (RANTES) increased in response to RV infection in Df mice, but not in PBS mice (P<0.05). The level of IL-10 significantly decreased following RV infection in Df mice (P<0.05).

conclusionOur findings suggest that the augmented induction of proinflammatory cytokines, Th2 cytokines, and chemokines that mediate an eosinophil response and the decreased induction of regulatory cytokines after RV infection may be important manifestations leading to airway inflammation with eosinophil infiltration and changes in airway responsiveness in the asthma model.

Indexed as

AsthmaExacerbationImmune responseRhinovirus

Identifiers

PMID24348661
PMCPMC3859881
OpenAlexW2106284392

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.