Evidence map›Paper›PMID 25595646›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2015

Enhanced inflammation in aged mice following infection with Streptococcus pneumoniae is associated with decreased IL-10 and augmented chemokine production.

Andrew E Williams, Ricardo J José, Jeremy S Brown, Rachel C Chambers

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. ImmunobioticInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Mouse Models forPathogens (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Cellular Senescence in Immunity against Infections.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Neutrophil Recruitment in Pneumococcal Pneumonia.Frontiers in cellular and infection microbiology · 2022
    Review
  13. Contribution of Puma to Inflammatory Resolution During Early Pneumococcal Pneumonia.Frontiers in cellular and infection microbiology · 2022
    Article
  14. Review
  15. Review
  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. 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

4 authors at 1 institution in 1 country.

Andrew E WilliamsCentre for Inflammation and Tissue Repair, Rayne Institute, University College London (UCL), London, United Kingdom.
Ricardo J JoséCentre for Inflammation and Tissue Repair, Rayne Institute, University College London (UCL), London, United Kingdom.
Jeremy S BrownCentre for Inflammation and Tissue Repair, Rayne Institute, University College London (UCL), London, United Kingdom.
Rachel C ChambersCentre for Inflammation and Tissue Repair, Rayne Institute, University College London (UCL), London, United Kingdom r.chambers@ucl.ac.uk.
University College London · GB

Funding

Medical Research Council G0800265Wellcome Trust 097216/Z/11/Z
6 · The paper itself

Abstract

Streptococcus pneumoniae is the most common cause of severe pneumonia in the elderly. However, the impact of aging on the innate inflammatory response to pneumococci is poorly defined. We compared the innate immune response in old vs. young adult mice following infection with S. pneumoniae. The accumulation of neutrophils recovered from bronchoalveolar lavage fluid and lung homogenates was increased in aged compared with young adult mice, although bacterial outgrowth was similar in both age groups, as were markers of microvascular leak. Aged mice had similar levels of IL-1β, TNF, IFN-γ, IL-17, and granulocyte colony-stimulating factor following S. pneumoniae infection, compared with young mice, but increased levels of the chemokines CXCL9, CXCL12, CCL3, CCL4, CCL5, CCL11, and CCL17. Moreover, levels of IL-10 were significantly lower in aged animals. Neutralization of IL-10 in infected young mice was associated with increased neutrophil recruitment but no decrease in bacterial outgrowth. Furthermore, IL-10 neutralization resulted in increased levels of CCL3, CCL5, and CXCL10. We conclude that aging is associated with enhanced inflammatory responses following S. pneumoniae infection as a result of a compromised immunomodulatory cytokine response.

Indexed as

AgingAnimalsChemokinesFemaleImmunomodulationInterleukin-10MiceMice, Inbred BALB CNeutrophil InfiltrationNeutrophilsPneumonia, PneumococcalStreptococcus pneumoniaeChemokinesIL10 protein, mouseInterleukin-10agingchemokineinflammationneutrophilpneumonia

Identifiers

PMID25595646
PMCPMC4360060
OpenAlexW1974374724

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.