Evidence map›Paper›PMID 22006566›Full record

ArticleInfection and immunity2012

Antibacterial role for natural killer cells in host defense to Bacillus anthracis.

Christine M Gonzales, Courtney B Williams, Veronica E Calderon, Matthew B Huante, Scott T Moen, Vsevolod L Popov, Wallace B Baze, Johnny W Peterson, Janice J Endsley

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

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  16. Cellular and physiological effects of anthrax exotoxin and its relevance to disease.Frontiers in cellular and infection microbiology · 2012
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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 2 institutions in 1 country.

Christine M GonzalesDepartment of Microbiology and Immunology, Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX, USA.
Courtney B Williams
Veronica E Calderon
Matthew B Huante
Scott T Moen
Vsevolod L Popov
Wallace B Baze
Johnny W Peterson
Janice J Endsley
The University of Texas Medical Branch at Galveston · USThe University of Texas MD Anderson Cancer Center · US

Funding

PREPing to a Biomedical PhDR25GM069285 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI VARGAS, GRACIE · 2009 to 2016
$2.3M
NIAID NIH HHS N01 AI030065NIAID NIH HHS N01-AI-30065NIGMS NIH HHS 1R25GM069285NIGMS NIH HHS R25 GM069285
6 · The paper itself

Abstract

Natural killer (NK) cells have innate antibacterial activity that could be targeted for clinical interventions for infectious disease caused by naturally occurring or weaponized bacterial pathogens. To determine a potential role for NK cells in immunity to Bacillus anthracis, we utilized primary human and murine NK cells, in vitro assays, and in vivo NK cell depletion in a murine model of inhalational anthrax. Our results demonstrate potent antibacterial activity by human NK cells against B. anthracis bacilli within infected autologous monocytes. Surprisingly, NK cells also mediate moderate antibacterial effects on extracellular vegetative bacilli but do not have activity against extracellular or intracellular spores. The immunosuppressive anthrax lethal toxin impairs NK gamma interferon (IFN-γ) expression, but neither lethal nor edema toxin significantly alters the viability or cytotoxic effector function of NK cells. Compared to human NK cells, murine NK cells have a similar, though less potent, activity against intracellular and extracellular B. anthracis. The in vivo depletion of murine NK cells does not alter animal survival following intranasal infection with B. anthracis spores in our studies but significantly increases the bacterial load in the blood of infected animals. Our studies demonstrate that NK cells participate in the innate immune response against B. anthracis and suggest that immune modulation to augment NK cell function in early stages of anthrax should be further explored in animal models as a clinical intervention strategy.

Indexed as

AdultAnimalsAnthraxAntigens, BacterialBacillus anthracisBacterial ToxinsCells, CulturedDisease Models, AnimalFemaleHumansInterferon-gammaKiller Cells, NaturalLeukocyte Reduction ProceduresMiceMiddle AgedSpores, Bacterialanthrax toxinAntigens, BacterialBacterial ToxinsInterferon-gamma

Identifiers

PMID22006566
PMCPMC3255656
OpenAlexW2142922581

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.