Evidence map›Paper›PMID 22299046›Full record

ArticlePloS one2012

Synergistic TLR2/6 and TLR9 activation protects mice against lethal influenza pneumonia.

Michael J Tuvim, Brian E Gilbert, Burton F Dickey, Scott E Evans

Abstract readEvaluation Study
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing 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

62 citing papers in PubMed.

  1. Journal of bacteriology · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Innate immune role of IL-6 in influenza a virus pathogenesis.Frontiers in cellular and infection microbiology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Epithelial STAT3: A New Twist in Inducible Antimicrobial Resistance.American journal of respiratory cell and molecular biology · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Minimizing caging effects in murine lung microbiome studies.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  19. Article
  20. Reply to YasumaAmerican journal of respiratory and critical care medicine · 2022
    Article

2 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

4 authors.

Michael J TuvimDepartment of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Brian E Gilbert
Burton F Dickey
Scott E Evans

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
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
NCI NIH HHS P30 CA016672NIAID NIH HHS U01 AI082226NIAID NIH HHS U01 AI82226
6 · The paper itself

Abstract

Lower respiratory tract infections caused by influenza A continue to exact unacceptable worldwide mortality, and recent epidemics have emphasized the importance of preventative and containment strategies. We have previously reported that induction of the lungs' intrinsic defenses by aerosolized treatments can protect mice against otherwise lethal challenges with influenza A virus. More recently, we identified a combination of Toll like receptor (TLR) agonists that can be aerosolized to protect mice against bacterial pneumonia. Here, we tested whether this combination of synthetic TLR agonists could enhance the survival of mice infected with influenza A/HK/8/68 (H3N2) or A/California/04/2009 (H1N1) influenza A viruses. We report that the TLR treatment enhanced survival whether given before or after the infectious challenge, and that protection tended to correlate with reductions in viral titer 4 d after infection. Surprisingly, protection was not associated with induction of interferon gene expression. Together, these studies suggest that synergistic TLR interactions can protect against influenza virus infections by mechanisms that may provide the basis for novel therapeutics.

Indexed as

AnimalsAntiviral AgentsDrug CombinationsDrug SynergismInfluenza A virusInfluenza A Virus, H1N1 SubtypeMiceOrthomyxoviridae InfectionsPneumonia, ViralSurvival AnalysisToll-Like Receptor 2Toll-Like Receptor 6Toll-Like Receptor 9ViremiaAntiviral AgentsDrug CombinationsTlr2 protein, mouseTlr6 protein, mouseTlr9 protein, mouseToll-Like Receptor 2Toll-Like Receptor 6Toll-Like Receptor 9

Identifiers

PMID22299046
PMCPMC3267724

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.