Evidence map›Paper›PMID 29097427›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2018

NLRP3 inflammasome activation in aged macrophages is diminished during Streptococcus pneumoniae infection.

Soo Jung Cho, Kristen Rooney, Augustine M K Choi, Heather W Stout-Delgado

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Nuclear dysfunction in aging and neurodegeneration.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  3. Functional Shift of NLRP3 Inflammasome Activity in Aged Macrophages.Bulletin of experimental biology and medicine · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Cellular Senescence in Immunity against Infections.International journal of molecular sciences · 2022
    Review
  13. Infection and immunity · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Macrophage LC3-associated phagocytosis is an immune defense againstProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Soo Jung ChoDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Weill Cornell Medicine , New York, New York.
Kristen RooneyDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Weill Cornell Medicine , New York, New York.
Augustine M K ChoiDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Weill Cornell Medicine , New York, New York.
Heather W Stout-DelgadoDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Weill Cornell Medicine , New York, New York.
Cornell University · USWeill Cornell Medicine · US

Funding

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 HL138285NIA 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

Pneumococcal infections are the eigth leading cause of death in the United States, and it is estimated that older patients (≥65 yr of age) account for the most serious cases. The goal of our current study is to understand the impact of biological aging on innate immune responses to Streptococcus pneumoniae, a causative agent of bacterial pneumonia. With the use of in vitro and in vivo aged murine models, our findings demonstrate that age-enhanced unfolded protein responses (UPRs) contribute to diminished inflammasome assembly and activation during S. pneumoniae infection. Pretreatment of aged mice with endoplasmic reticulum chaperone and the stress-reducing agent tauroursodeoxycholic acid (TUDCA) decreased mortality in aged hosts that was associated with increased NLRP3 inflammasome activation, improved pathogen clearance, and decreased pneumonitis during infection. Taken together, our data provide new evidence as to why older persons are more susceptible to S. pneumoniae and provide a possible therapeutic target to decrease morbidity and mortality in this population.

Indexed as

AgedAnimalsCells, CulturedFemaleHost-Pathogen InteractionsHumansImmunity, InnateInflammasomesMacrophagesMaleMiceMice, Inbred BALB CMice, Inbred C57BLNLR Family, Pyrin Domain-Containing 3 ProteinPneumococcal InfectionsSignal TransductionInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mouseagingER stressinflammasomemacrophagepneumonia

Identifiers

PMID29097427
PMCPMC5900358
OpenAlexW2767180543

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.