Evidence map›Paper›PMID 26944087›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2016

Dissecting the inflammatory twitch in allergically inflamed mice.

Joshua J Pothen, Matthew E Poynter, Lennart K A Lundblad, Jason H T Bates

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Pathophysiology to Phenotype in the Asthma of Obesity.Annals of the American Thoracic Society · 2017
    Review
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

4 authors.

Joshua J PothenDepartment of Medicine, University of Vermont College of Medicine, Burlington, Vermont.
Matthew E PoynterDepartment of Medicine, University of Vermont College of Medicine, Burlington, Vermont.
Lennart K A LundbladDepartment of Medicine, University of Vermont College of Medicine, Burlington, Vermont.
Jason H T BatesDepartment of Medicine, University of Vermont College of Medicine, Burlington, Vermont jason.h.bates@med.uvm.edu.

Funding

Multidisciplinary Training in Lung BiologyT32HL076122 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI IRVIN, CHARLES G, POYNTER, MATTHEW E · 2004 to 2023
$6.1M
Translational Research in Lung Biology and DiseaseP30GM103532 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI IRVIN, CHARLES G · 2012 to 2016
$3.7M
A multi-scale approach to airway hyperresponsiveness: from molecule to organR01HL103405 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BATES, JASON HT, LAUZON, ANNE-MARIE · 2010 to 2013
$3.6M
iNKT Cells Regulating Lung Mast Cells: New Treatment Opportunity for AsthmaR21AI112804 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI LUNDBLAD, LENNART KARL ALF · 2014 to 2015
$419k
The Inflammatory Twitch: Discerning the Nature of Chronic Inflammatory DiseasesF31EB018215 · NIBIB · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI POTHEN, JOSHUA JEREMY · 2014 to 2015
$81k
NHLBI NIH HHS R01 HL103405NHLBI NIH HHS T32 HL076122NIAID NIH HHS R21 AI112804NIBIB NIH HHS F31 EB018215NIGMS NIH HHS P30 GM103532
6 · The paper itself

Abstract

We have previously advanced the hypothesis that the allergic inflammatory response in the lungs occurs as a self-limited sequence of events that begins with the onset of inflammation and then resolves back to baseline over a predetermined time course (Pothen JJ, Poynter ME, Bates JH. J Immunol 190: 3510-3516, 2013). In the present study we tested a key prediction of this hypothesis, which is that the instigation of the allergic inflammatory response should be accompanied by a later refractory period during which the response cannot be reinitiated. We challenged groups of ovalbumin-sensitized BALB/c mice for 3, 14, 21 and 31 consecutive days with aerosolized ovalbumin. We measured airways responsiveness as well as cell counts and cytokines in bronchoalveolar lavage fluid after the final challenge in subgroups from each group. In other subgroups we performed the same measurements following rest periods and after a final single recall challenge with antigen. We determined that the refractory periods for GM-CSF, KC, and IL-5 are no longer than 10 days, while those for IFNγ and IL-10 are no longer than 28 days. The refractory periods for total leukocytes and neutrophils were no greater than 28 days, while that for eosinophils was more than 28 days. The refractory period for airways resistance was less than 17, while for lung elastance it was longer than 28 days. Our results thus demonstrate that the components of the allergic inflammatory response in the lung have finite refractory periods, with the refractory period of the entire response being in the order of a month.

Indexed as

AnimalsAsthmaCytokinesFemaleLeukocyte CountLungMice, Inbred BALB CPneumoniaCytokinesbronchoalveolar lavagecytokineslung functionrefractory period

Identifiers

PMID26944087
PMCPMC4896098

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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.