Evidence map›Paper›PMID 25606048›Full record

ArticleImmunity & ageing : I & A2014

Genetically diverse mice are novel and valuable models of age-associated susceptibility to Mycobacterium tuberculosis.

David E Harrison, Clinton M Astle, M Khalid Khan Niazi, Samuel Major, Gillian L Beamer

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Methods and Models for StudyingInternational journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. The chosen few:Frontiers in immunology · 2024
    Review
  10. Article
  11. Article
  12. Animal models for COVID-19 and tuberculosis.Frontiers in immunology · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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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

5 authors at 3 institutions in 1 country.

David E Harrison *The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609 USA.
Clinton M AstleThe Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609 USA.
M Khalid Khan NiaziThe Ohio State University, Columbus, OH 43210 USA.
Samuel MajorTufts University Cummings School of Veterinary Medicine, 200 Westboro Road, Grafton, MA 01536 USA.
Gillian L Beamer *Tufts University Cummings School of Veterinary Medicine, 200 Westboro Road, Grafton, MA 01536 USA.
Jackson Laboratory · USTufts University · USThe Ohio State University · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Interventions That Retard Mammalian AgingU01AG022308 · NIA · JACKSON LABORATORY · PI Ronny Korstanje · 2003 to 2026
$30.5M
Genetic Definition of Mechanisms by which Rapamycin Retards Mammalian AgingR01AG038560 · NIA · JACKSON LABORATORY · PI HARRISON, DAVID E · 2011 to 2015
$1.8M
Lifespan Extension Despite Greatly Elevated Insulin and Body FatR01AG032333 · NIA · JACKSON LABORATORY · PI HARRISON, DAVID E · 2010 to 2014
$1.8M
NCI NIH HHS P30 CA034196NIA NIH HHS R01 AG032333NIA NIH HHS R01 AG038560NIA NIH HHS U01 AG022308
6 · The paper itself

Abstract

backgroundTuberculosis, the disease due to Mycobacterium tuberculosis, is an important cause of morbidity and mortality in the elderly. Use of mouse models may accelerate insight into the disease and tests of therapies since mice age thirty times faster than humans. However, the majority of TB research relies on inbred mouse strains, and these results might not extrapolate well to the genetically diverse human population. We report here the first tests of M. tuberculosis infection in genetically heterogeneous aging mice, testing if old mice benefit from rapamycin.

findingsWe find that genetically diverse aging mice are much more susceptible than young mice to M. tuberculosis, as are aging human beings. We also find that rapamycin boosts immune responses during primary infection but fails to increase survival.

conclusionsGenetically diverse mouse models provide a valuable resource to study how age influences responses and susceptibility to pathogens and to test interventions. Additionally, surrogate markers such as immune measures may not predict whether interventions improve survival.

Indexed as

Diversity outbredDOEarly Secreted Antigenic Target-6 (ESAT-6)Genetically diverse populationHET3RapamycinTuberculosis

Identifiers

PMID25606048
PMCPMC4299371
OpenAlexW2131393876

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.