Evidence map›Paper›PMID 27019327›Full record

ArticleNature medicine2016

Commensal microbiota affects ischemic stroke outcome by regulating intestinal γδ T cells.

Corinne Benakis, David Brea, Silvia Caballero, Giuseppe Faraco, Jamie Moore, Michelle Murphy, Giulia Sita, Gianfranco Racchumi, Lilan Ling, Eric G Pamer and 2 more

Abstract read
In one paragraph

Article in Nature medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 688 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
688citing papers in PubMed, 3 pooled it
37.6field-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

688 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,067 citations in OpenAlex.

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  14. Immune-mediated excitotoxicity in brain disorders.Nature reviews. Immunology · 2026
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628 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Corinne BenakisFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
David BreaFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Silvia CaballeroImmunology Program and Infectious Disease Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Giuseppe FaracoFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Jamie MooreFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Michelle MurphyFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Giulia SitaFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Gianfranco RacchumiFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Lilan LingLucille Castori Center for Microbes, Inflammation and Cancer, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Eric G PamerImmunology Program and Infectious Disease Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Costantino IadecolaFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Josef AnratherFeil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York, USA.
Cornell University · USMIND Research Institute · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NO SYNTHASE GENE EXPRESSION AND CEREBRAL ISCHEMIC DAMAGER01NS034179 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IADECOLA, COSTANTINO · 1995 to 2021
$5.5M
Protective monocytes in cerebral ischemic toleranceR01NS081179 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANRATHER, JOSEF · 2012 to 2022
$3.7M
NCI NIH HHS P30 CA008748NINDS NIH HHS R01 NS034179NINDS NIH HHS R01 NS081179
6 · The paper itself

Abstract

Commensal gut bacteria impact the host immune system and can influence disease processes in several organs, including the brain. However, it remains unclear whether the microbiota has an impact on the outcome of acute brain injury. Here we show that antibiotic-induced alterations in the intestinal flora reduce ischemic brain injury in mice, an effect transmissible by fecal transplants. Intestinal dysbiosis alters immune homeostasis in the small intestine, leading to an increase in regulatory T cells and a reduction in interleukin (IL)-17-positive γδ T cells through altered dendritic cell activity. Dysbiosis suppresses trafficking of effector T cells from the gut to the leptomeninges after stroke. Additionally, IL-10 and IL-17 are required for the neuroprotection afforded by intestinal dysbiosis. The findings reveal a previously unrecognized gut-brain axis and an impact of the intestinal flora and meningeal IL-17(+) γδ T cells on ischemic injury.

Indexed as

AnimalsAnti-Bacterial AgentsBehavior, AnimalBlood-Brain BarrierBrainBrain IschemiaDendritic CellsDysbiosisFecal Microbiota TransplantationFlow CytometryGastrointestinal MicrobiomeImmunity, MucosalImmunohistochemistryInfarction, Middle Cerebral ArteryInterleukin-10Interleukin-17Anti-Bacterial AgentsIL10 protein, mouseInterleukin-10Interleukin-17Receptors, Antigen, T-Cell, gamma-deltaRNA, MessengerRNA, Ribosomal, 16S

Identifiers

PMID27019327
PMCPMC4860105
OpenAlexW2332044667

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.