Evidence map›Paper›PMID 19362023›Full record

ArticleImmunity2009

The intracellular sensor NLRP3 mediates key innate and healing responses to influenza A virus via the regulation of caspase-1.

Paul G Thomas, Pradyot Dash, Jerry R Aldridge, Ali H Ellebedy, Cory Reynolds, Amy J Funk, William J Martin, Mohamed Lamkanfi, Richard J Webby, Kelli L Boyd and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 459 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
459citing papers in PubMed, 2 pooled it
35.6field-weighted citation impact, top 1% 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

459 citing papers in PubMed, 2 syntheses or guidelines pooled it, 743 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Mitochondrial double-stranded RNA fuels pancreatic cancer growth via RIG-I/TLR3 inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. The temporal sequence of influenza H1N1 andFrontiers in microbiology · 2026
    Article
  12. Article
  13. IFI204 RestrictsMicroorganisms · 2025
    Article
  14. Regulation of inflammatory processes by caspases.Nature reviews. Molecular cell biology · 2025
    Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. ZBP1-driven cell death in severe influenza.Trends in microbiology · 2025
    Review

399 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 at 2 institutions in 2 countries.

Paul G ThomasDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Pradyot Dash
Jerry R Aldridge
Ali H Ellebedy
Cory Reynolds
Amy J Funk
William J Martin
Mohamed Lamkanfi
Richard J Webby
Kelli L Boyd
Peter C Doherty
Thirumala-Devi Kanneganti
St. Jude Children's Research Hospital · USUniversity of Melbourne · AU

Funding

Role of NLR Inflammasomes in Autoinflammatory Diseases and Host DefenseR01AR056296 · NIAMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KANNEGANTI, THIRUMALA-DEVI · 2008 to 2022
$5.9M
Protective Cell-Mediated Immunity Against Lethal H5N1 Influenza A VirusesR01AI070251 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DOHERTY, PETER C · 2006 to 2010
$2.0M
Antigen-specific CD4+ T cell responses to influenzaF32AI065097 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI THOMAS, PAUL GLYNDWR · 2005 to 2007
$143k
Role of dendritic cells in lethal H5N1 influenza infectionF32AI078667 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI ALDRIDGE, JERRY R · 2009 to 2010
$106k
NIAID NIH HHS AI065097NIAID NIH HHS AI170251NIAID NIH HHS F32 AI065097NIAID NIH HHS F32 AI078667NIAID NIH HHS HHSN266200700005CNIAID NIH HHS R01 AI070251NIAMS NIH HHS AR056296NIAMS NIH HHS R01 AR056296
6 · The paper itself

Abstract

Virus-induced interlukin-1beta (IL-1beta) and IL-18 production in macrophages are mediated via caspase-1 pathway. Multiple microbial components, including viral RNA, are thought to trigger assembly of the cryopyrin inflammasome resulting in caspase-1 activation. Here, we demonstrated that Nlrp3(-/-) and Casp1(-/-) mice were more susceptible than wild-type mice after infection with a pathogenic influenza A virus. This enhanced morbidity correlated with decreased neutrophil and monocyte recruitment and reduced cytokine and chemokine production. Despite the effect on innate immunity, cryopyrin-deficiency was not associated with any obvious defect in virus control or on the later emergence of the adaptive response. Early epithelial necrosis was, however, more severe in the infected mutants, with extensive collagen deposition leading to later respiratory compromise. These findings reveal a function of the cryopyrin inflammasome in healing responses. Thus, cryopyrin and caspase-1 are central to both innate immunity and to moderating lung pathology in influenza pneumonia.

Indexed as

Immunity, InnateAnimalsAntigen-Presenting CellsCarrier ProteinsCaspase 1Cells, CulturedGene Expression RegulationGenetic Predisposition to DiseaseInfluenza A virusInterleukin-1betaMiceMice, Inbred C57BLMice, KnockoutNLR Family, Pyrin Domain-Containing 3 ProteinCarrier ProteinsCaspase 1Interleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouse

Identifiers

PMID19362023
PMCPMC2765464
OpenAlexW1975296966

What OpenQuestion holds

Textmetadata
LicenceTDM
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.