Evidence map›Paper›PMID 29471332›Full record

ArticleThe Journal of infectious diseases2018

Mycobacterium tuberculosis-Infected Hematopoietic Stem and Progenitor Cells Unable to Express Inducible Nitric Oxide Synthase Propagate Tuberculosis in Mice.

Stephen T Reece, Alexis Vogelzang, Julia Tornack, Wolfgang Bauer, Ulrike Zedler, Sandra Schommer-Leitner, Georg Stingl, Fritz Melchers, Stefan H E Kaufmann

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 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
1.4field-weighted citation impact, top 21% 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, 21 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Detection ofThe Lancet. Microbe · 2021
    Observational
  7. Review
  8. Detection ofAAS open research · 2020
    Article
  9. Article
  10. [New vaccines against tuberculosis].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2020
    Review
  11. Targeting innate immunity for tuberculosis vaccination.The Journal of clinical investigation · 2019
    Review
  12. Review
  13. Article
  14. Review
  15. Review
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

9 authors at 2 institutions in 2 countries.

Stephen T ReeceDepartment of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Alexis VogelzangDepartment of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Julia TornackSenior Group on Lymphocyte Development, Max Planck Institute for Infection Biology, Berlin, Germany.
Wolfgang BauerDivision of Immunology, Allergy and Infectious Diseases, Department of Dermatology, Medical University of Vienna, Austria.
Ulrike ZedlerDepartment of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Sandra Schommer-LeitnerDepartment of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Georg StinglDivision of Immunology, Allergy and Infectious Diseases, Department of Dermatology, Medical University of Vienna, Austria.
Fritz MelchersSenior Group on Lymphocyte Development, Max Planck Institute for Infection Biology, Berlin, Germany.
Stefan H E KaufmannDepartment of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Max Planck Institute for Infection Biology · DEMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistence of Mycobacterium tuberculosis within human bone marrow stem cells has been identified as a potential bacterial niche during latent tuberculosis. Using a murine model of tuberculosis, we show here that bone marrow stem and progenitor cells containing M. tuberculosis propagated tuberculosis when transferred to naive mice, given that both transferred cells and recipient mice were unable to express inducible nitric oxide synthase, which mediates killing of intracellular bacteria via nitric oxide. Our findings suggest that bone marrow stem and progenitor cells containing M. tuberculosis propagate hallmarks of disease if nitric oxide-mediated killing of bacteria is defective.

Indexed as

AnimalsDisease Models, AnimalHematopoietic Stem CellsHematopoietic Stem Cell TransplantationMiceMice, Inbred C57BLMycobacterium tuberculosisNitric OxideNitric Oxide Synthase Type IIStem CellsTuberculosisNitric OxideNitric Oxide Synthase Type II

Identifiers

PMID29471332
PMCPMC5913604
OpenAlexW2791315694

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.