Evidence map›Paper›PMID 29807129›Full record

ArticleBrain, behavior, and immunity2018

Immunization with Mycobacterium vaccae induces an anti-inflammatory milieu in the CNS: Attenuation of stress-induced microglial priming, alarmins and anxiety-like behavior.

Matthew G Frank, Laura K Fonken, Samuel D Dolzani, Jessica L Annis, Philip H Siebler, Dominic Schmidt, Linda R Watkins, Steven F Maier, Christopher A Lowry

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 84 citations in OpenAlex.

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  13. Effects ofInternational journal of molecular sciences · 2023
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  16. International journal of molecular sciences · 2023
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  20. Interactions between gut microbes and NLRP3 inflammasome in the gut-brain axis.Computational and structural biotechnology journal · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Matthew G FrankDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA; Center for Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA. Electronic address: matt.frank@colorado.edu.
Laura K FonkenDivision of Pharmacology and Toxicology, University of Texas at Austin, Austin, TX 78712, USA.
Samuel D DolzaniDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA; Center for Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA.
Jessica L AnnisDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA; Center for Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA.
Philip H SieblerDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO 80309, USA.
Dominic SchmidtDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO 80309, USA.
Linda R WatkinsDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA; Center for Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA.
Steven F MaierDepartment of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA; Center for Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA.
Christopher A LowryCenter for Neuroscience, University of Colorado Boulder, Boulder, CO 80309, USA; Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO 80309, USA; Department of Physical Medicine & Rehabilitation, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Center for Neuroscience, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Rocky Mountain Mental Illness Research Education and Clinical Center (MIRECC), Denver Veterans Affairs Medical Center (VAMC), Denver, CO 80220, USA; Military and Veteran Microbiome Consortium for Research and Education (MVM-CoRE), Denver, CO 80220, USA.
University of Colorado Boulder · USMental Illness Research, Education and Clinical Centers · USThe University of Texas at Austin · US

Funding

Stress-induced neuroinflammatory priming: Glucocorticoids, inflammasomes, alarminsR01MH108523 · NIMH · UNIVERSITY OF COLORADO · PI MAIER, STEVEN F · 2016 to 2020
$2.1M
Mycobacterium vaccae and stress resilience: Neural mechanismsR21MH116263 · NIMH · UNIVERSITY OF COLORADO · PI FRANK, MATTHEW G, LOWRY, CHRISTOPHER A · 2018 to 2019
$424k
The role of the NLRP3 inflammasome in aging-associated cognitive impairmentsF32AG048672 · NIA · UNIVERSITY OF COLORADO · PI FONKEN, LAURA K · 2014 to 2016
$164k
Biological Signature and Safety of an Immunomodulatory Probiotic Intervention for Veterans with Co-Occuring Mild TBI and PTSDI21RX002232 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI BRENNER, LISA A · 2016 to 2018
–
NIA NIH HHS F32 AG048672NIMH NIH HHS R01 MH108523NIMH NIH HHS R21 MH116263RRD VA I21 RX002232
6 · The paper itself

Abstract

Exposure to stressors induces anxiety- and depressive-like behaviors, which are mediated, in part, by neuroinflammatory processes. Recent findings demonstrate that treatment with the immunoregulatory and anti-inflammatory bacterium, Mycobacterium vaccae (M. vaccae), attenuates stress-induced exaggeration of peripheral inflammation and stress-induced anxiety-like behavioral responses. However, the effects of M. vaccae on neuroimmune processes have largely been unexplored. In the present study, we examined the effect of M. vaccae NCTC11659 on neuroimmune regulation, stress-induced neuroinflammatory processes and anxiety-like behavior. Adult male rats were immunized 3× with a heat-killed preparation of M. vaccae (0.1 mg, s.c.) or vehicle. M. vaccae induced an anti-inflammatory immunophenotype in hippocampus (increased interleukin (Il)4, Cd200r1, and Mrc1 mRNA expression) and increased IL4 protein 8 d after the last immunization. Central administration of recombinant IL4 recapitulated the effects of M. vaccae on Cd200r1 and Mrc1 mRNA expression. M. vaccae reduced basal levels of genes (Nlrp3 and Nfkbia) involved in microglial priming; thus, we explored the effects of M. vaccae on stress-induced hippocampal microglial priming and HMGB1, which mediates priming. We found that M. vaccae blocked stress-induced decreases in Cd200r1, increases in the alarmin HMGB1, and priming of the microglial response to immune challenge. Furthermore, M. vaccae prevented stress-induced increases in anxiety-like behavior. The present findings suggest that M. vaccae enhances immunomodulation in the CNS and mitigates the neuroinflammatory and behavioral effects of stress, which may underpin its capacity to impart a stress resilient phenotype.

Indexed as

AlarminsAnimalsAnti-Inflammatory AgentsAnxietyCentral Nervous SystemHippocampusHMGB1 ProteinImmunizationInflammationMaleMicrogliaMycobacteriumNLR Family, Pyrin Domain-Containing 3 ProteinRatsRats, Sprague-DawleyStress, PsychologicalAlarminsAnti-Inflammatory AgentsHMGB1 ProteinNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratAlarminImmunoregulationMicrogliaM. vaccaeNeuroinflammationStress

Identifiers

PMID29807129
PMCPMC6129419
OpenAlexW2803672518

What OpenQuestion holds

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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.