Evidence map›Paper›PMID 31060958›Full record

ReviewTuberculosis (Edinburgh, Scotland)2019

Mycobacterium tuberculosis and macrophage nuclear receptors: What we do and don't know.

Chrissy M Leopold Wager, Eusondia Arnett, Larry S Schlesinger

Open access · greenAbstract readReview
In one paragraph

Review in Tuberculosis (Edinburgh, Scotland), 2019. 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
1.5field-weighted citation impact, top 18% 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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. PPARγ AmelioratesFrontiers in microbiology · 2022
    Article
  6. Pathogenesis of SARS-CoV-2 andFrontiers in immunology · 2022
    Review
  7. Review
  8. Editorial: Host immune evasion byFrontiers in immunology · 2022
    Article
  9. Article
  10. MicroRNA‑502‑3p promotesMolecular medicine reports · 2021
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  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

3 authors at 1 institution in 1 country.

Chrissy M Leopold WagerTexas Biomedical Research Institute, San Antonio, TX, USA. Electronic address: cwager@txbiomed.org.
Eusondia ArnettTexas Biomedical Research Institute, San Antonio, TX, USA. Electronic address: earnett@txbiomed.org.
Larry S SchlesingerTexas Biomedical Research Institute, San Antonio, TX, USA. Electronic address: lschlesinger@txbiomed.org.
Texas Biomedical Research Institute · US

Funding

TB and Innate Immune Regulation of Lung MacrophagesR01AI059639 · NIAID · OHIO STATE UNIVERSITY · PI SCHLESINGER, LARRY S. · 2005 to 2016
$3.2M
Interferon Regulation in Systemic LupusR01AI059636 · NIAID · HOSPITAL FOR SPECIAL SURGERY · PI IVASHKIV, LIONEL B · 2006 to 2010
$2.0M
Altered Mycobacterium tuberculosis Mannosylation and the MacrophageR01AI052458 · NIAID · OHIO STATE UNIVERSITY · PI SCHLESINGER, LARRY S. · 2006 to 2010
$1.8M
Altered M. tuberculosis Mannosylation and the MacrophageR21AI052458 · NIAID · UNIVERSITY OF IOWA · PI SCHLESINGER, LARRY S. · 2002 to 2002
$283k
NIAID NIH HHS R01 AI052458NIAID NIH HHS R01 AI059636NIAID NIH HHS R01 AI059639NIAID NIH HHS R21 AI052458
6 · The paper itself

Abstract

Nuclear receptors (NRs) are ligand-activated transcription factors that are expressed in a wide variety of cells and play a major role in lipid signaling. NRs are key regulators of immune and metabolic functions in macrophages and are linked to macrophage responses to microbial pathogens. Pathogens are also known to induce the expression of specific NRs to promote their own survival. In this review, we focus on the NRs recently shown to influence macrophage responses to Mycobacterium tuberculosis (M.tb), a significant cause of morbidity and mortality worldwide. We provide an overview of NR-controlled transcriptional activity and regulation of macrophage activation. We also discuss in detail the contribution of specific NRs to macrophage responses to M.tb, including influence on macrophage phenotype, cell signaling, and cellular metabolism. We pay particular attention to PPARγ since it is required for differentiation of alveolar macrophages, an important niche for M.tb, and its role during M.tb infection is becoming increasingly appreciated. Research into NRs and M.tb is still in its early stages, therefore continuing to advance our understanding of the complex interactions between M.tb and macrophage NRs may reveal the potential of NRs as pharmacological targets for the treatment of tuberculosis.

Indexed as

AnimalsCell NucleusHost-Pathogen InteractionsHumansMacrophage ActivationMacrophagesMycobacterium tuberculosisPPAR gammaSignal TransductionTuberculosisPPAR gammaPPARG protein, humanMacrophageMycobacterium tuberculosisNuclear receptorsPPARγ

Identifiers

PMID31060958
PMCPMC6750772
OpenAlexW2941239879

What OpenQuestion holds

Textmetadata
LicenceTDM
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.