Evidence map›Paper›PMID 19329554›Full record

ArticleAmerican journal of respiratory cell and molecular biology2010

Stimulated innate resistance of lung epithelium protects mice broadly against bacteria and fungi.

Scott E Evans, Brenton L Scott, Cecilia G Clement, Derek T Larson, Dimitrios Kontoyiannis, Russell E Lewis, P Rocco Lasala, Jennifer Pawlik, Johnny W Peterson, Ashok K Chopra and 6 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02148796 (Randomized, Placebo-controlled, Multicenter Study to Assess the Efficacy, Safety and Tolerability of ORal Bacterial EXtract for the Prevention of Wheezing Lower Respiratory Tract Illness), which is not on this map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
4.2field-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.

NCT02148796 phase2completednot on this mapstarted 2017, after this paper: background citation

Randomized, Placebo-controlled, Multicenter Study to Assess the Efficacy, Safety and Tolerability of ORal Bacterial EXtract for the Prevention of Wheezing Lower Respiratory Tract Illness (ORBEX)

TypeinterventionalSponsorUniversity of ArizonaRan2017 to 2026Enrolled822ConditionsAsthma, WheezingArmsBroncho-Vaxom (BV), Placebo
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Epithelial STAT3: A New Twist in Inducible Antimicrobial Resistance.American journal of respiratory cell and molecular biology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The effect of aerosolized bacterial lysate on experimentally inducedCanadian journal of veterinary research = Revue canadienne de recherche veterinaire · 2022
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. CD8American journal of respiratory cell and molecular biology · 2020
    Article
  19. Inducible Epithelial Resistance against Coronavirus Pneumonia in Mice.American journal of respiratory cell and molecular biology · 2020
    Article
  20. Article

17 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

16 authors at 3 institutions in 1 country.

Scott E EvansDepartment of Pulmonary Medicine, M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030-4009, USA. seevans@mdanderson.org
Brenton L Scott
Cecilia G Clement
Derek T Larson
Dimitrios Kontoyiannis
Russell E Lewis
P Rocco Lasala
Jennifer Pawlik
Johnny W Peterson
Ashok K Chopra
Gary Klimpel
Gabriela Bowden
Magnus Höök
Yi Xu
Michael J Tuvim
Burton F Dickey
Texas A&M Health Science Center · USThe University of Texas MD Anderson Cancer Center · USThe University of Texas Medical Branch at Galveston · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
Modeling Airway Lung Cancer and the Role of InflammationU01CA105352 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DEMAYO, FRANCESCO JOHN · 2004 to 2008
$4.2M
Identification of New Antigens for a Plague VaccineR01AI064389 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CHOPRA, ASHOK K · 2005 to 2015
$3.8M
Development of Therapeutic Inhibitors to Anthrax ToxinsU01AI053858 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI PETERSON, JOHNNY WAYNE · 2002 to 2006
$2.5M
Stimulated Innate Resistance of the Lungs to Bioterror pathogensU01AI082226 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HOOK, AXEL MAGNUS · 2009 to 2013
$2.2M
Munc18 Proteins in Airway Mucus HypersecretionR01HL072984 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DICKEY, BURTON F · 2003 to 2006
$1.5M
CONFERENCE: ANTIGEN AND CLONE-SPECIFIC IMMUNOREGULATIONR13AI030065 · NIAID · NEW YORK ACADEMY OF SCIENCES · PI EDELSON, RICHARD L · 1990 to 1990
–
STEM ANALYTICAL ELECTRON MICROSCOPE SYSTEMS10RR002419 · NCRR · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI MORSE, DENNIS E · 1985 to 1985
–
NCI NIH HHS CA105352NCI NIH HHS P30CA16672NCRR NIH HHS KL2-RR-02419NHLBI NIH HHS HL072984NIAID NIH HHS AI064389NIAID NIH HHS AI15437NIAID NIH HHS AI30065NIAID NIH HHS AI 5385802NIAID NIH HHS U01 AI082226
6 · The paper itself

Abstract

Pneumonia is a serious problem worldwide. We recently demonstrated that innate defense mechanisms of the lung are highly inducible against pneumococcal pneumonia. To determine the breadth of protection conferred by stimulation of lung mucosal innate immunity, and to identify cells and signaling pathways activated by this treatment, mice were treated with an aerosolized bacterial lysate, then challenged with lethal doses of bacterial and fungal pathogens. Mice were highly protected against a broad array of Gram-positive, Gram-negative, and class A bioterror bacterial pathogens, and the fungal pathogen, Aspergillus fumigatus. Protection was associated with rapid pathogen killing within the lungs, and this effect was recapitulated in vitro using a respiratory epithelial cell line. Gene expression analysis of lung tissue showed marked activation of NF-kappaB, type I and II IFN, and antifungal Card9-Bcl10-Malt1 pathways. Cytokines were the most strongly induced genes, but the inflammatory cytokines TNF and IL-6 were not required for protection. Lung-expressed antimicrobial peptides were also highly up-regulated. Taken together, stimulated innate resistance appears to occur through the activation of multiple host defense signaling pathways in lung epithelial cells, inducing rapid pathogen killing, and conferring broad protection against virulent bacterial and fungal pathogens. Augmentation of innate antimicrobial defenses of the lungs might have therapeutic value for protection of patients with neutropenia or impaired adaptive immunity against opportunistic pneumonia, and for defense of immunocompetent subjects against a bioterror threat or epidemic respiratory infection.

Indexed as

Immunity, InnateAerosolsAnimalsBacterial InfectionsEpithelial CellsFemaleGene Expression RegulationInflammationLungMaleMiceMice, Inbred C57BLMycosesPneumoniaTime FactorsAerosols

Identifiers

PMID19329554
PMCPMC2809220
OpenAlexW2106845589

What OpenQuestion holds

Textmetadata
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.