Evidence map›Paper›PMID 34830070›Full record

ArticleInternational journal of molecular sciences2021

The Effect of Tuberculosis Antimicrobials on the Immunometabolic Profiles of Primary Human Macrophages Stimulated with

Christina Cahill, Dónal J Cox, Fiona O'Connell, Sharee A Basdeo, Karl M Gogan, Cilian Ó'Maoldomhnaigh, Jacintha O'Sullivan, Joseph Keane, James J Phelan

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. New Drugs and Novel Cellular Targets against Tuberculosis.International journal of molecular sciences · 2022
    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

9 authors at 1 institution in 1 country.

Christina CahillTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.ORCID 0000-0002-2472-9627
Dónal J CoxTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.ORCID 0000-0002-8523-3836
Fiona O'ConnellDepartment of Surgery, Trinity Translational Medicine Institute, Trinity College Dublin, St James's Hospital, Dublin 8, Ireland.ORCID 0000-0002-3641-4374
Sharee A BasdeoTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.ORCID 0000-0001-5616-6665
Karl M GoganTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.
Cilian Ó'MaoldomhnaighTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.
Jacintha O'SullivanDepartment of Surgery, Trinity Translational Medicine Institute, Trinity College Dublin, St James's Hospital, Dublin 8, Ireland.
Joseph KeaneTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.
James J PhelanTB Immunology Group, Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College, Dublin, Ireland.ORCID 0000-0001-9431-2002
Trinity College Dublin · IE

Funding

Irish Research Council GOIPD/2020/16Science Foundation Ireland 18/TIDA/6026The Royal City of Dublin Hospital Trust BaggotStreetHospital/Dublin 4/Ireland
6 · The paper itself

Abstract

Tuberculosis (TB) remains a global health challenge. Patients with drug-sensitive and drug-resistant TB undergo long, arduous, and complex treatment regimens, often involving multiple antimicrobials. While these drugs were initially implemented based on their bactericidal effects, some studies show that TB antimicrobials can also directly affect cells of the immune system, altering their immune function. As use of these antimicrobials has been the mainstay of TB therapy for over fifty years now, it is more important than ever to understand how these antimicrobials affect key pathways of the immune system. One such central pathway, which underpins the immune response to a variety of infections, is immunometabolism, namely glycolysis and oxidative phosphorylation (OXPHOS). We hypothesise that in addition to their direct bactericidal effect on

Indexed as

Antitubercular AgentsClofazimineCytokinesGlycolysisHumansLipopolysaccharidesMacrophagesMitochondriaMycobacterium tuberculosisOxidative PhosphorylationPrimary Cell CultureTuberculosisAntitubercular AgentsClofazimineCytokinesLipopolysaccharidesantimicrobialsbioenergeticsdrug-resistant tuberculosisglycolysishost-directed therapylipopolysaccharidemitochondrial functionoxidative phosphorylationtuberculosis

Identifiers

PMID34830070
PMCPMC8624646
OpenAlexW3214725693

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.