Evidence map›Paper›PMID 24958709›Full record

ArticleInfection and immunity2014

Allergic airway inflammation decreases lung bacterial burden following acute Klebsiella pneumoniae infection in a neutrophil- and CCL8-dependent manner.

Daniel E Dulek, Dawn C Newcomb, Kasia Goleniewska, Jaqueline Cephus, Weisong Zhou, Sara Reiss, Shinji Toki, Fei Ye, Rinat Zaynagetdinov, Taylor P Sherrill and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. IL-33-mediated Eosinophilia Protects against Acute Lung Injury.American journal of respiratory cell and molecular biology · 2021
    Article
  10. Can Eosinophils Prevent Lung Injury? Ask PHIL.American journal of respiratory cell and molecular biology · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Allergic Asthma FavorsFrontiers in immunology · 2018
    Article
  16. Article
  17. Cell-free hemoglobin: a novel mediator of acute lung injury.American journal of physiology. Lung cellular and molecular physiology · 2016
    Article
  18. Article
  19. Allergen-encoded signals that control allergic responses.Current opinion in allergy and clinical immunology · 2016
    Review
  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

15 authors at 3 institutions in 1 country.

Daniel E DulekDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Dawn C NewcombDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Kasia GoleniewskaDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Jaqueline CephusDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Weisong ZhouDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Sara ReissDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Shinji TokiDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Fei YeDepartment of Biostatistics and Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Rinat ZaynagetdinovDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Taylor P SherrillDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Timothy S BlackwellDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Martin L MooreDepartment of Pediatrics, Emory University, and Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Kelli L BoydDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Jay K KollsDepartment of Pediatrics, University of Pittsburgh, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
R Stokes PeeblesDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA stokes.peebles@vanderbilt.edu.
Vanderbilt University Medical Center · USChildren's Hospital of Pittsburgh · USEmory University · US

Funding

Viral and Host Determinants of Infant and Childhood Allergy and AsthmaU19AI095227 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Christian Rosas-Salazar · 2011 to 2026
$34.9M
Building Interdisciplinary Research Careers in Women's HealthK12HD043483 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARTMANN, KATHERINE E, MAJOR, AMY S · 2002 to 2023
$10.3M
Immunobiology of Blood and Vascular Systems Training ProgramT32HL069765 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2002 to 2016
$6.5M
Interdisciplinary Training Program in Lung ResearchT32HL094296 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ray Stokes Peebles · 2008 to 2026
$6.3M
Conducting Child Health Care Research in Vulnerable PopulationsT32HD060554 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BARKIN, SHARI, WILLIAMS, DEREK J. · 2009 to 2019
$3.8M
PGI2 regulation of TSLP-mediated allergic inflammation in the lungR01AI111820 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PEEBLES, RAY STOKES · 2014 to 2018
$2.0M
The Role of PGI2 in Allergic InflammationR01HL090664 · NHLBI · VANDERBILT UNIVERSITY · PI PEEBLES, RAY STOKES · 2009 to 2013
$1.9M
The role of cyclooxygenase in the adaptive immune response and toleranceI01BX000624 · VA · VETERANS HEALTH ADMINISTRATION · PI PEEBLES, RAY STOKES · 2009 to 2019
–
BLRD VA I01 BX000624NHLBI NIH HHS R01 HL090664NHLBI NIH HHS R01HL090664NHLBI NIH HHS T32 HL069765NHLBI NIH HHS T32 HL094296NHLBI NIH HHS T32HL094296NIAID NIH HHS R01 AI111820NIAID NIH HHS R01AI111820NIAID NIH HHS U19 AI095227NIAID NIH HHS U19AI095227NICHD NIH HHS K12 HD043483NICHD NIH HHS T32 HD060554NICHD NIH HHS T32HD060554
6 · The paper itself

Abstract

The Th17 cytokines interleukin-17A (IL-17A), IL-17F, and IL-22 are critical for the lung immune response to a variety of bacterial pathogens, including Klebsiella pneumoniae. Th2 cytokine expression in the airways is a characteristic feature of asthma and allergic airway inflammation. The Th2 cytokines IL-4 and IL-13 diminish ex vivo and in vivo IL-17A protein expression by Th17 cells. To determine the effect of IL-4 and IL-13 on IL-17-dependent lung immune responses to acute bacterial infection, we developed a combined model in which allergic airway inflammation and lung IL-4 and IL-13 expression were induced by ovalbumin sensitization and challenge prior to acute lung infection with K. pneumoniae. We hypothesized that preexisting allergic airway inflammation decreases lung IL-17A expression and airway neutrophil recruitment in response to acute K. pneumoniae infection and thereby increases the lung K. pneumoniae burden. As hypothesized, we found that allergic airway inflammation decreased the number of K. pneumoniae-induced airway neutrophils and lung IL-17A, IL-17F, and IL-22 expression. Despite the marked reduction in postinfection airway neutrophilia and lung expression of Th17 cytokines, allergic airway inflammation significantly decreased the lung K. pneumoniae burden and postinfection mortality. We showed that the decreased lung K. pneumoniae burden was independent of IL-4, IL-5, and IL-17A and partially dependent on IL-13 and STAT6. Additionally, we demonstrated that the decreased lung K. pneumoniae burden associated with allergic airway inflammation was both neutrophil and CCL8 dependent. These findings suggest a novel role for CCL8 in lung antibacterial immunity against K. pneumoniae and suggest new mechanisms of orchestrating lung antibacterial immunity.

Indexed as

AnimalsChemokine CCL8EosinophilsFemaleHypersensitivityInflammationInterleukinsKlebsiella InfectionsKlebsiella pneumoniaeLungMiceMice, Inbred BALB CNeutrophilsOvalbuminPneumonia, BacterialCcl8 protein, mouseChemokine CCL8InterleukinsOvalbumin

Identifiers

PMID24958709
PMCPMC4187810
OpenAlexW2124408542

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.