Evidence map›Paper›PMID 35185874›Full record

ArticleFrontiers in immunology2022

Regulation of Peripheral Inflammation by a Non-Viable, Non-Colonizing Strain of Commensal Bacteria.

Kritika Ramani, Taylor Cormack, Adam N R Cartwright, Aula Alami, Pooja Parameswaran, Marynawal Abdou, Iris Wang, Kristie Hilliard-Barth, Shannon Argueta, Divya Raghunathan and 13 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

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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

23 authors.

Kritika RamaniEvelo Biosciences, Cambridge, MA, United States.
Taylor CormackEvelo Biosciences, Cambridge, MA, United States.
Adam N R CartwrightEvelo Biosciences, Cambridge, MA, United States.
Aula AlamiEvelo Biosciences, Cambridge, MA, United States.
Pooja ParameswaranEvelo Biosciences, Cambridge, MA, United States.
Marynawal AbdouEvelo Biosciences, Cambridge, MA, United States.
Iris WangEvelo Biosciences, Cambridge, MA, United States.
Kristie Hilliard-BarthEvelo Biosciences, Cambridge, MA, United States.
Shannon ArguetaEvelo Biosciences, Cambridge, MA, United States.
Divya RaghunathanEvelo Biosciences, Cambridge, MA, United States.
Will CaffryEvelo Biosciences, Cambridge, MA, United States.
Christopher J H DavittEvelo Biosciences, Cambridge, MA, United States.
Fabian B RomanoEvelo Biosciences, Cambridge, MA, United States.
Aylwin NgEvelo Biosciences, Cambridge, MA, United States.
Valeria KravitzEvelo Biosciences, Cambridge, MA, United States.
Tyler RommelEvelo Biosciences, Cambridge, MA, United States.
Maria SizovaEvelo Biosciences, Cambridge, MA, United States.
Esra Uckun KiranEvelo Biosciences, Cambridge, MA, United States.
Pallavi PradeepEvelo Biosciences, Cambridge, MA, United States.
Holly E PonichteraEvelo Biosciences, Cambridge, MA, United States.
Tanmoy GangulyEvelo Biosciences, Cambridge, MA, United States.
Mark BodmerEvelo Biosciences, Cambridge, MA, United States.
Andrea ItanoEvelo Biosciences, Cambridge, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gastrointestinal tract represents one of the largest body surfaces that is exposed to the outside world. It is the only mucosal surface that is required to simultaneously recognize and defend against pathogens, while allowing nutrients containing foreign antigens to be tolerated and absorbed. It differentiates between these foreign substances through a complex system of pattern recognition receptors expressed on the surface of the intestinal epithelial cells as well as the underlying immune cells. These immune cells actively sample and evaluate microbes and other particles that pass through the lumen of the gut. This local sensing system is part of a broader distributed signaling system that is connected to the rest of the body through the enteric nervous system, the immune system, and the metabolic system. While local tissue homeostasis is maintained by commensal bacteria that colonize the gut, colonization itself may not be required for the activation of distributed signaling networks that can result in modulation of peripheral inflammation. Herein, we describe the ability of a gut-restricted strain of commensal bacteria to drive systemic anti-inflammatory effects in a manner that does not rely upon its ability to colonize the gastrointestinal tract or alter the mucosal microbiome. Orally administered EDP1867, a gamma-irradiated strain of

Indexed as

AnimalsAnti-Bacterial AgentsBacteriaCytokinesEpithelial CellsFemaleGastrointestinal MicrobiomeHumansImmunity, MucosalInflammationIntestinal MucosaMiceMice, Inbred BALB CMice, Inbred C57BLSymbiosisT-LymphocytesAnti-Bacterial AgentsCytokinesbacteriaCNSgastrointestinal tractinflammationTh1Th17Th2

Identifiers

PMID35185874
PMCPMC8847375
OpenAlexW4210568034

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.