Evidence map›Paper›PMID 26409283›Full record

ReviewClinical infectious diseases : an official publication of the Infectious Diseases Society of America2015

Immune Cell Regulatory Pathways Unexplored as Host-Directed Therapeutic Targets for Mycobacterium tuberculosis: An Opportunity to Apply Precision Medicine Innovations to Infectious Diseases.

Robert N Mahon, Richard Hafner

Abstract readReview
In one paragraph

Review in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. The Role of mTOR inBiomedicines · 2024
    Review
  3. Article
  4. Different modalities of host cell death and their impact onAmerican journal of physiology. Cell physiology · 2022
    Review
  5. Frontiers in immunology · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Remembering the Host in Tuberculosis Drug Development.The Journal of infectious diseases · 2019
    Review
  10. The pathogenesis of tuberculous meningitis.Journal of leukocyte biology · 2019
    Review
  11. Stem cell-based Lung-on-Chips: The best of both worlds?Advanced drug delivery reviews · 2019
    Review
  12. Review
  13. eLife · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Statin adjunctive therapy shortens the duration of TB treatment in mice.The Journal of antimicrobial chemotherapy · 2016
    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

2 authors.

Robert N MahonDivision of AIDS-Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc, Contractor to the National Institute of Allergy and Infectious Diseases, National Institutes of Health.
Richard HafnerDivision of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.

Funding

NIAID NIH HHS HHSN272200800014CPHS HHS HHSN272200800014C
6 · The paper itself

Abstract

The lack of novel antimicrobial drugs in development for tuberculosis treatment has provided an impetus for the discovery of adjunctive host-directed therapies (HDTs). Several promising HDT candidates are being evaluated, but major advancement of tuberculosis HDTs will require understanding of the master or "core" cell signaling pathways that control intersecting immunologic and metabolic regulatory mechanisms, collectively described as "immunometabolism." Core regulatory pathways conserved in all eukaryotic cells include poly (ADP-ribose) polymerases (PARPs), sirtuins, AMP-activated protein kinase (AMPK), and mechanistic target of rapamycin (mTOR) signaling. Critical interactions of these signaling pathways with each other and their roles as master regulators of immunometabolic functions will be addressed, as well as how Mycobacterium tuberculosis is already known to influence various other cell signaling pathways interacting with them. Knowledge of these essential mechanisms of cell function regulation has led to breakthrough targeted treatment advances for many diseases, most prominently in oncology. Leveraging these exciting advances in precision medicine for the development of innovative next-generation HDTs may lead to entirely new paradigms for treatment and prevention of tuberculosis and other infectious diseases.

Indexed as

Precision MedicineAMP-Activated Protein KinasesAntitubercular AgentsHumansMycobacterium tuberculosisPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesSignal TransductionSirtuinsTOR Serine-Threonine KinasesTuberculosisAMP-Activated Protein KinasesAntitubercular AgentsMTOR protein, humanPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesSirtuinsTOR Serine-Threonine Kinaseshost-directed therapyimmunometabolismprecision medicinesignaling pathwaystuberculosis

Identifiers

PMID26409283
PMCPMC4583576

What OpenQuestion holds

Textmetadata
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.