Evidence map›Paper›PMID 18388354›Full record

ArticleAmerican journal of respiratory and critical care medicine2008

Stimulation of lung innate immunity protects against lethal pneumococcal pneumonia in mice.

Cecilia G Clement, Scott E Evans, Christopher M Evans, David Hawke, Ryuji Kobayashi, Paul R Reynolds, Seyed J Moghaddam, Brenton L Scott, Ernestina Melicoff, Roberto Adachi and 2 more

Abstract readEvaluation Study
In one paragraph

Article in American journal of respiratory and critical care medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
–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

70 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  8. The effect of aerosolized bacterial lysate on experimentally inducedCanadian journal of veterinary research = Revue canadienne de recherche veterinaire · 2022
    Article
  9. Article
  10. Article
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  12. The Role of Innate Immunity in Pulmonary Infections.BioMed research international · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Animal Models ofInternational journal of molecular sciences · 2019
    Review
  19. Article
  20. Review

10 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

12 authors.

Cecilia G ClementDepartment of Pulmonary Medicine, M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030-4009. USA.
Scott E Evans
Christopher M Evans
David Hawke
Ryuji Kobayashi
Paul R Reynolds
Seyed J Moghaddam
Brenton L Scott
Ernestina Melicoff
Roberto Adachi
Burton F Dickey
Michael J Tuvim

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 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
Munc18 Proteins in Airway Mucus HypersecretionR01HL072984 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DICKEY, BURTON F · 2003 to 2006
$1.5M
NCI NIH HHS CA016672NCI NIH HHS CA105352NHLBI NIH HHS HL072984
6 · The paper itself

Abstract

rationaleThe lungs are a common site of serious infection in both healthy and immunocompromised subjects, and the most likely route of delivery of a bioterror agent. Since the airway epithelium shows great structural plasticity in response to inflammatory stimuli, we hypothesized it might also show functional plasticity.

objectivesTo test the inducibility of lung defenses against bacterial challenge.

methodsMice were treated with an aerosolized lysate of ultraviolet-killed nontypeable (unencapsulated) Haemophilus influenzae (NTHi), then challenged with a lethal dose of live Streptococcus pneumoniae (Spn) delivered by aerosol. MEASUREMENTS AND MAIN

resultsTreatment with the NTHi lysate induced complete protection against challenge with a lethal dose of Spn if treatment preceded challenge by 4 to 24 hours. Lesser levels of protection occurred at shorter (83% at 2 h) and longer (83% at 48-72 h) intervals between treatment and challenge. There was also some protection when treatment was given 2 hours after challenge (survival increased from 14 to 57%), but not 24 hours after challenge. Protection did not depend on recruited neutrophils or resident mast cells and alveolar macrophages. Protection was specific to the airway route of infection, correlated in magnitude and time with rapid bacterial killing within the lungs, and was associated with increases of multiple antimicrobial polypeptides in lung lining fluid.

conclusionsWe infer that protection derives from stimulation of local innate immune mechanisms, and that activated lung epithelium is the most likely cellular effector of this response. Augmentation of innate antimicrobial defenses of the lungs might have therapeutic value.

Indexed as

Immunity, InnateAdjuvants, ImmunologicAerosolsAnimalsBacteriaBacterial LysatesBronchoalveolar Lavage FluidCell ExtractsColony Count, MicrobialDose-Response Relationship, ImmunologicFemaleImmunocompromised HostMiceMice, Inbred BALB CNeutrophil InfiltrationPneumonia, PneumococcalAdjuvants, ImmunologicAerosolsBacterial LysatesBroncho-VaxomCell Extracts

Identifiers

PMID18388354
PMCPMC2427056

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.