Evidence map›Paper›PMID 29203400›Full record

ArticleExperimental gerontology2018

Decreased NLRP3 inflammasome expression in aged lung may contribute to increased susceptibility to secondary Streptococcus pneumoniae infection.

Soo Jung Cho, Maria Plataki, Dana Mitzel, Gena Lowry, Kristen Rooney, Heather Stout-Delgado

Abstract read
In one paragraph

Article in Experimental gerontology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
  5. Article
  6. Article
  7. The Role of Innate Immunity in Pulmonary Infections.BioMed research international · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. How Inflammation Blunts Innate Immunity in Aging.Interdisciplinary topics in gerontology and geriatrics · 2020
    Review
  14. Article
  15. 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

6 authors at 2 institutions in 1 country.

Soo Jung ChoDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Weill Cornell Medicine, New York, NY, United States.
Maria PlatakiDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Weill Cornell Medicine, New York, NY, United States.
Dana MitzelLovelace Respiratory Research Institute, Albuquerque, NM, United States.
Gena LowryLovelace Respiratory Research Institute, Albuquerque, NM, United States.
Kristen RooneyDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Weill Cornell Medicine, New York, NY, United States.
Heather Stout-DelgadoDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Weill Cornell Medicine, New York, NY, United States. Electronic address: hes2019@med.cornell.edu.
Cornell University · USLovelace Respiratory Research Institute · US

Funding

T32: Pathogenesis of Infectious Diseases Training ProgramT32AI007613 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ROY M. GULICK · 1999 to 2026
$8.8M
Impact of Heightened ER Stress on NLRP3 Activation in Aged Lung during InfectionR01AG052530 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI STOUT DELGADO, HEATHER WINONA · 2017 to 2021
$2.1M
GLUT1-dependent glycolysis regulates age-susceptible lung fibrosisK08HL138285 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHO, SOO JUNG · 2017 to 2021
$829k
Aging with Chronic Viral Infections and the Impact on Innate Immune ResponsesK01AG034999 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI STOUT DELGADO, HEATHER WINONA · 2011 to 2015
$687k
Detection & Use of Novel Therapeutics to Stimulate NLRP3 Activity in the ElderlyR21AG044755 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI STOUT DELGADO, HEATHER WINONA · 2013 to 2014
$507k
NHLBI NIH HHS K08 HL138285NIAID NIH HHS T32 AI007613NIA NIH HHS K01 AG034999NIA NIH HHS L30 AG043118NIA NIH HHS L30 AG057058NIA NIH HHS R01 AG052530NIA NIH HHS R21 AG044755
6 · The paper itself

Abstract

Post-viral pneumococcal pneumonia is a leading morbidity and mortality in older patients (≥65years of age). The goal of our current study is to understand the impact of chronological aging on innate immune responses to a secondary, post viral infection with Streptococcus pneumoniae, a causative agent of bacterial pneumonia. Using aged murine models of infection, our findings demonstrate increased morbidity and mortality in aged mice within 48h post-secondary S. pneumoniae infection. Increased susceptibility of aged mice was associated with decreased TLR1, TLR6, and TLR9 mRNA expression and diminished IL1β mRNA expression. Examination of NLRP3 inflammasome expression illustrated decreased NLRP3 mRNA expression and decreased IL1β production in aged lung in response to secondary S. pneumoniae infection.

Indexed as

AgingAnimalsDisease Models, AnimalFemaleHost-Pathogen InteractionsImmunity, InnateInflammasomesInterleukin-1betaLungMaleMiceMice, Inbred BALB CNLR Family, Pyrin Domain-Containing 3 ProteinPneumonia, PneumococcalStreptococcus pneumoniaeToll-Like Receptor 1InflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseTlr6 protein, mouseTlr9 protein, mouseToll-Like Receptor 1Toll-Like Receptor 6Toll-Like Receptor 9

Identifiers

PMID29203400
PMCPMC5869149
OpenAlexW2774746035

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.