Evidence map›Paper›PMID 28235016›Full record

ArticlePloS one2017

The dual role of short fatty acid chains in the pathogenesis of autoimmune disease models.

Miho Mizuno, Daisuke Noto, Naoko Kaga, Asako Chiba, Sachiko Miyake

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed, 2 pooled it
8.3field-weighted citation impact, top 2% 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

145 citing papers in PubMed, 2 syntheses or guidelines pooled it, 228 citations in OpenAlex.

  1. Changes in Gut Microbiota and Multiple Sclerosis: A Systematic Review.International journal of environmental research and public health · 2023
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  11. Dose-dependent protective effects ofFrontiers in pharmacology · 2026
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85 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

5 authors at 1 institution in 1 country.

Miho MizunoDepartment of Immunology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, Japan.
Daisuke NotoDepartment of Immunology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, Japan.
Naoko KagaLaboratory of Proteomics and Biomolecular Science Research Support Center, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Asako ChibaDepartment of Immunology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, Japan.
Sachiko MiyakeDepartment of Immunology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, Japan.
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune diseases are influenced by both genetic and environmental factors. The gut environment has attracted much attention as an essential component that modulates immune responses, and therefore immune-mediated disorders, such as autoimmune diseases. Growing evidence suggests that microbiota and their metabolites are critical factors for immune modulation. Recently, we reported that the microbiome in patients with multiple sclerosis, an autoimmune disease targeting the myelin sheath of the central nervous system, is characterized by a reduction of bacteria belonging to Clostridia clusters IV and XIVa, which are potent producers of short-chain fatty acids (SCFAs) by fermentation of indigestible carbohydrates. In the present study, we investigated the role of SCFAs in the regulation of inflammation. We demonstrated that oral administration of SCFAs ameliorated the disease severity of systemic autoimmune inflammatory conditions mediated by lymphocytes such as experimental autoimmune encephalitis and collagen-induced arthritis. Amelioration of disease was associated with a reduction of Th1 cells and an increase in regulatory T cells. In contrast, SCFAs contributed to the exaggeration of K/BxN serum transfer arthritis, representing the effector phase of inflammation in rheumatoid arthritis. An increased understanding of the effect of microbiota metabolites will lead to the effective treatment and prevention of systemic inflammatory disorders.

Indexed as

Administration, OralAnimalsAnti-Inflammatory AgentsArthritis, ExperimentalDrug Evaluation, PreclinicalEncephalomyelitis, Autoimmune, ExperimentalFatty Acids, VolatileMice, Inbred C57BLMice, Inbred DBAMice, TransgenicTh1 CellsT-Lymphocytes, RegulatoryAnti-Inflammatory AgentsFatty Acids, Volatile

Identifiers

PMID28235016
PMCPMC5325617
OpenAlexW2589854016

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.