Evidence map›Paper›PMID 28273087›Full record

ArticlePloS one2017

An aerosol challenge model of tuberculosis in Mauritian cynomolgus macaques.

S A Sharpe, A D White, L Sibley, F Gleeson, G A Hall, R J Basaraba, A McIntyre, S O Clark, K Gooch, P D Marsh and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. One Size Fits All? Not inFrontiers in cellular and infection microbiology · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. 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

12 authors at 3 institutions in 2 countries.

S A SharpePublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
A D WhitePublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
L SibleyPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
F GleesonThe Churchill Hospital, Headington, Oxford, United Kingdom.
G A HallPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
R J BasarabaDepartment of Microbiology Immunology and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America.
A McIntyreThe Churchill Hospital, Headington, Oxford, United Kingdom.
S O ClarkPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
K GoochPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
P D MarshPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
A WilliamsPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
M J DennisPublic Health England, National Infection Service, Porton Down, Salisbury, SP4 0JG, United Kingdom.
Public Health England · GBChurchill Hospital · GBColorado State University · US

Funding

Disrupting Biofilm Formation to Improve TB Drug TreatmentR01AI106733 · NIAID · COLORADO STATE UNIVERSITY · PI BASARABA, RANDALL J · 2013 to 2017
$2.3M
Therapeutic Restoration of Metabolic Homeostasis During Active TBR21AI107254 · NIAID · COLORADO STATE UNIVERSITY · PI BASARABA, RANDALL J · 2014 to 2015
$409k
NIAID NIH HHS R01 AI106733NIAID NIH HHS R21 AI107254
6 · The paper itself

Abstract

backgroundNew interventions for tuberculosis are urgently needed. Non-human primate (NHP) models provide the most relevant pre-clinical models of human disease and play a critical role in vaccine development. Models utilising Asian cynomolgus macaque populations are well established but the restricted genetic diversity of the Mauritian cynomolgus macaques may be of added value.

methodsMauritian cynomolgus macaques were exposed to a range of doses of M. tuberculosis delivered by aerosol, and the outcome was assessed using clinical, imaging and pathology-based measures.

resultsAll macaques developed characteristic clinical signs and disease features of tuberculosis (TB). Disease burden and the ability to control disease were dependent on exposure dose. Mauritian cynomolgus macaques showed less variation in pulmonary disease burden and total gross pathology scores within exposure dose groups than either Indian rhesus macaques or Chinese cynomolgus macaques.

conclusionsThe genetic homogeneity of Mauritian cynomolgus macaques makes them a potentially useful model of human tuberculosis.

Indexed as

AnimalsEnzyme-Linked Immunospot AssayInterferon-gammaKidneyLiverLungMacaca fascicularisMagnetic Resonance ImagingMycobacterium tuberculosisRadiography, ThoracicSeverity of Illness IndexTuberculosisInterferon-gamma

Identifiers

PMID28273087
PMCPMC5342172
OpenAlexW2591640539

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.