Evidence map›Paper›PMID 39606220›Full record

ArticleFrontiers in immunology2024

Longitudinal mitochondrial bioenergetic signatures of blood monocytes and lymphocytes improve during treatment of drug-susceptible pulmonary tuberculosis patients Monocyte/lymphocyte bioenergetic signatures post-TB treatment.

Bridgette M Cumming, Kelvin W Addicott, Fernanda Maruri, Vanessa Pillay, Rukaya Asmal, Sashen Moodley, Beatriz Barreto-Durate, Mariana Araújo-Pereira, Matilda Mazibuko, Zoey Mhlane and 12 more

Erratum issuedAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Bridgette M CummingAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Kelvin W AddicottAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Fernanda MaruriVanderbilt Tuberculosis Center, Vanderbilt University School of Medicine, Nashville, TN, United States.
Vanessa PillayAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Rukaya AsmalAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Sashen MoodleyAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Beatriz Barreto-DurateMultinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Salvador, Brazil.
Mariana Araújo-PereiraMultinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Salvador, Brazil.
Matilda MazibukoAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Zoey MhlaneAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Nikiwe MbathaAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Khadija KhanAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Senamile MakhariAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Farina KarimAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Lauren PeetlukVanderbilt Tuberculosis Center, Vanderbilt University School of Medicine, Nashville, TN, United States.
Alexander S PymAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Mahomed Yunus S MoosaDepartment of Infectious Diseases, University of KwaZulu-Natal, Durban, South Africa.
Yuri F van der HeijdenVanderbilt Tuberculosis Center, Vanderbilt University School of Medicine, Nashville, TN, United States.
Timothy S SterlingVanderbilt Tuberculosis Center, Vanderbilt University School of Medicine, Nashville, TN, United States.
Bruno B AndradeMultinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Salvador, Brazil.
Alasdair LeslieAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Adrie J C SteynAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.

Funding

CCASAnet: Caribbean, Central and South America NetworkU01AI069923 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Pedro Enrique Cahn, Jessica L Castilho · 2006 to 2026
$41.6M
A Global Research Resource for Human TuberculosisR24AI186591 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ADRIE JC STEYN · 2024 to 2026
$3.5M
Hydrogen Sulfide and Tuberculosis DiseaseR01AI134810 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STEYN, ADRIE JC · 2018 to 2021
$2.2M
Interplay between the Mtb electron transport chain and carbon metabolismR01AI137043 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STEYN, ADRIE JC · 2019 to 2023
$2.1M
METABOLIC REPROGRAMMING OF T CELL ENERGY METABOLISM IN TUBERCULOSIS AND HIVR61AI138280 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STEYN, ADRIE JC · 2018 to 2019
$1.0M
Fluoroquinolone resistance in patients with multidrug-resistant tuberculosisK08AI106420 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI VAN DER HEIJDEN, YURI F. · 2014 to 2018
$848k
NIAID NIH HHS K08 AI106420NIAID NIH HHS R01 AI134810NIAID NIH HHS R01 AI137043NIAID NIH HHS R24 AI186591NIAID NIH HHS R61 AI138280NIAID NIH HHS U01 AI069923Wellcome Trust
6 · The paper itself

Abstract

The impact of human pulmonary tuberculosis (TB) on the bioenergetic metabolism of circulating immune cells remains elusive, as does the resolution of these effects with TB treatment. In this study, the rates of oxidative phosphorylation (OXPHOS) and glycolysis in circulating lymphocytes and monocytes of patients with drug-susceptible TB at diagnosis, 2 months, and 6 months during treatment, and 12 months after diagnosis were investigated using extracellular flux analysis. At diagnosis, the bioenergetic parameters of both blood lymphocytes and monocytes of TB patients were severely impaired in comparison to non-TB and non-HIV-infected controls. However, most bioenergetic parameters were not affected by HIV status or glycemic index. Treatment of TB patients restored the % spare respiratory capacity (%SRC) of the circulating lymphocytes to that observed in non-TB and non-HIV infected controls by 12 months. Treatment also improved the maximal respiration of circulating lymphocytes and the %SRC of circulating monocytes of the TB patients. Notably, the differential correlation of the clinical and bioenergetic parameters of the monocytes and lymphocytes from the controls and TB patients at baseline and month 12 was consistent with improved metabolic health and resolution of inflammation following successful TB treatment. Network analysis of the bioenergetic parameters of circulating immune cells with serum cytokine levels indicated a highly coordinated immune response at month 6. These findings underscore the importance of metabolic health in combating TB, supporting the need for further investigation of the bioenergetic immunometabolism associated with TB infection for novel therapeutic approaches aimed at bolstering cellular energetics to enhance immune responses and expedite recovery in TB patients.

Indexed as

Antitubercular AgentsEnergy MetabolismLymphocytesMitochondriaMonocytesTuberculosis, PulmonaryAdultFemaleGlycolysisHIV InfectionsHumansLongitudinal StudiesMaleMiddle AgedOxidative PhosphorylationYoung AdultAntitubercular Agentsbioenergetic metabolismcytokineslymphocytesmonocytesSeahorse XF96TB treatmenttuberculosis

Identifiers

PMID39606220
PMCPMC11599235

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Registered trials

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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.