Evidence map›Paper›PMID 26500648›Full record

ReviewFrontiers in immunology2015

Mechanisms of Control of Mycobacterium tuberculosis by NK Cells: Role of Glutathione.

Michael Allen, Cedric Bailey, Ian Cahatol, Levi Dodge, Jay Yim, Christine Kassissa, Jennifer Luong, Sarah Kasko, Shalin Pandya, Vishwanath Venketaraman

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

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  14. Loss of circulating CD8αbioRxiv : the preprint server for biology · 2024
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6 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

10 authors at 1 institution in 1 country.

Michael AllenCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Cedric BaileyCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Ian CahatolCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Levi DodgeCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Jay YimCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Christine KassissaCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Jennifer LuongCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Sarah KaskoCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Shalin PandyaCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA.
Vishwanath VenketaramanCollege of Osteopathic Medicine of the Pacific, Western University of Health Sciences , Pomona, CA , USA ; Department of Basic Medical Sciences, Western University of Health Sciences , Pomona, CA , USA.
Western University of Health Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB), caused by Mycobacterium tuberculosis (M. tb), continues to be one of the most prevalent infectious diseases in the world. There is an upward trend in occurrence due to emerging multidrug resistant strains and an increasingly larger proportion of immunocompromised patient populations as a result of the acquired immunodeficiency syndrome pandemic. The complex and often deadly combination of multidrug resistant M. tb (MDR-M. tb) along with human immunodeficiency virus (HIV) puts a significant number of people at high risk for pulmonary and extra-pulmonary TB without sufficient therapeutic options available. Natural killer (NK) cells and macrophages are major components of the body's innate immune system, contributing significantly to the body's ability to synergistically inhibit the growth of M. tb in immune compromised individuals lacking a sufficient T cell response. Direct mechanisms of control are largely through the secretory products perforin, granulysin, and granzymes, as well as multiple membrane-bound death receptors that facilitate target directed lysis. NK cells also have a role in indirectly stimulating an immune response through activation of macrophages and monocytes with multiple signaling pathways, including both reactive oxygen species and reactive nitrogen species. Glutathione (GSH) has been shown to play a part in inhibiting the growth of intracellular M. tb through bacteriostatic mechanisms. Enhancing cellular GSH through several cytokines and N-acetyl cysteine has been shown to increase these effects, at least in part, through their action on NK cells. Taken together, there is substantial evidence for a mechanistic correlation between NK cell activity and functionality in combating M. tb in HIV infection mediated through adequate GSH production and use.

Indexed as

AIDS-related opportunistic infectionsglutathioneHIV infectionsinnate immunitymacrophagesMycobacterium tuberculosisnatural killer cells

Identifiers

PMID26500648
PMCPMC4593255
OpenAlexW1884998774

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.