Evidence map›Paper›PMID 19802565›Full record

ReviewCurrent topics in microbiology and immunology2009

Autophagy in immunity against mycobacterium tuberculosis: a model system to dissect immunological roles of autophagy.

Vojo Deretic, Monica Delgado, Isabelle Vergne, Sharon Master, Sergio De Haro, Marisa Ponpuak, Sudha Singh

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in microbiology and immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
42.7field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 130 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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  5. Review
  6. Review
  7. Article
  8. TheFrontiers in immunology · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Frontiers in immunology · 2021
    Review
  14. Screening forFrontiers in cellular and infection microbiology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Manipulation of autophagy for host-directed tuberculosis therapy.African journal of thoracic and critical care medicine · 2019
    Review
  19. Review
  20. Review

12 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Vojo DereticDepartment of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, 915 Camino de Salud NE, Albuquerque, NM 87131, USA, vderetic@salud.unm.edu
Monica Delgado
Isabelle Vergne
Sharon Master
Sergio De Haro
Marisa Ponpuak
Sudha Singh
University of New Mexico · US

Funding

Pattern Recognition Receptors and Autophagy in Mtb Control in AIDSR01AI042999 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI DERETIC, VOJO P · 1998 to 2017
$6.6M
Pattern Recognition Receptors and Autophagy in Mtb Control in AIDSR37AI042999 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI VOJO P DERETIC · 2018 to 2026
$4.7M
MECHANISM OF M TUBERCULOSIS PHAGOSOME MATURATION ARRESTR01AI045148 · NIAID · UNIVERSITY OF NEW MEXICO · PI DERETIC, VOJO P · 1999 to 2008
$3.3M
Autophagy in TuberculosisR01AI069345 · NIAID · UNIVERSITY OF NEW MEXICO · PI DERETIC, VOJO P · 2007 to 2011
$1.8M
Autophagy and Crohn's DiseaseRC1AI086845 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI DERETIC, VOJO P, MA, THOMAS Y · 2009 to 2010
$1.0M
NIAID NIH HHS R01 AI042999NIAID NIH HHS R01 AI045148NIAID NIH HHS R01 AI069345NIAID NIH HHS R37 AI042999NIAID NIH HHS RC1 AI086845
6 · The paper itself

Abstract

The recognition of autophagy as an immune mechanism has been affirmed in recent years. One of the model systems that has helped in the development of our current understanding of how autophagy and more traditional immunity systems cooperate in defense against intracellular pathogens is macrophage infection with Mycobacterium tuberculosis. M. tuberculosis is a highly significant human pathogen that latently infects billions of people and causes active disease in millions of patients worldwide. The ability of the tubercle bacillus to persist in human populations rests upon its macrophage parasitism. One of the initial reports on the ability of autophagy to act as a cell-autonomous innate immunity mechanism capable of eliminating intracellular bacteria was on M. tuberculosis. This model system has further contributed to the recognition of multiple connections between conventional immune regulators and autophagy. In this chapter, we will review how these studies have helped to establish the following principles: (1) autophagy functions as an innate defense mechanism against intracellular microbes; (2) autophagy is under the control of pattern recognition receptors (PRR) such as Toll-like receptors (TLR), and it acts as one of the immunological output effectors of PRR and TLR signaling; (3) autophagy is one of the effector functions associated with the immunity-regulated GTPases, which were initially characterized as molecules involved in cell-autonomous defense, but whose mechanism of function was unknown until recently; (4) autophagy is an immune effector of Th1/Th2 T cell response polarization-autophagy is activated by Th1 cytokines (which act in defense against intracellular pathogens) and is inhibited by Th2 cytokines (which make cells accessible to intracellular pathogens). Collectively, the studies employing the M. tuberculosis autophagy model system have contributed to the development of a more comprehensive view of autophagy as an immunological process. This work and related studies by others have led us to propose a model of how autophagy, an ancient innate immunity defense, became integrated over the course of evolution with other immune mechanisms of ever-increasing complexity.

Indexed as

AnimalsAutophagyHumansImmunity, InnateMycobacterium tuberculosisReceptors, Pattern RecognitionTh1 CellsTh2 CellsToll-Like ReceptorsTuberculosisReceptors, Pattern RecognitionToll-Like Receptors

Identifiers

PMID19802565
PMCPMC2788935
OpenAlexW1526489492

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.