Evidence map›Paper›PMID 29078267›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Gut dysbiosis breaks immunological tolerance toward the central nervous system during young adulthood.

Sudhir K Yadav, Sridhar Boppana, Naoko Ito, John E Mindur, Martin T Mathay, Ankoor Patel, Suhayl Dhib-Jalbut, Kouichi Ito

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  5. Review
  6. Article
  7. Review
  8. Exploring the effect of gut microbiome on Alzheimer's disease.Biochemistry and biophysics reports · 2024
    Review
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  14. Article
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  17. Article
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  20. Immunoregulatory Effects of Tolerogenic Probiotics in Multiple Sclerosis.Advances in experimental medicine and biology · 2021
    Review
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

8 authors at 4 institutions in 1 country.

Sudhir K YadavDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
Sridhar BoppanaDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
Naoko ItoDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
John E MindurDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
Martin T MathayDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
Ankoor PatelDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
Suhayl Dhib-JalbutDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854.
Kouichi ItoDepartment of Neurology, Rutgers-Robert Wood Johnson Medical School, Piscataway, NJ 08854; itoko@rwjms.rutgers.edu.
Rutgers, The State University of New Jersey · USJohnson University · USCenter for Systems Biology · USDelaware State University · US

Funding

Human Keratin (K14)-MBP/MBP-TCR Transgenic Animal ModelR21AI067474 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ITO, KOUICHI · 2008 to 2009
$407k
NIAID NIH HHS R21 AI067474
6 · The paper itself

Abstract

Multiple sclerosis (MS) is an autoimmune disease targeting the central nervous system (CNS) mainly in young adults, and a breakage of immune tolerance to CNS self-antigens has been suggested to initiate CNS autoimmunity. Age and microbial infection are well-known factors involved in the development of autoimmune diseases, including MS. Recent studies have suggested that alterations in the gut microbiota, referred to as dysbiosis, are associated with MS. However, it is still largely unknown how gut dysbiosis affects the onset and progression of CNS autoimmunity. In this study, we investigated the effects of age and gut dysbiosis on the development of CNS autoimmunity in humanized transgenic mice expressing the MS-associated MHC class II (MHC-II) gene, HLA-DR2a, and T-cell receptor (TCR) genes specific for MBP87-99/DR2a that were derived from an MS patient. We show here that the induction of gut dysbiosis triggers the development of spontaneous experimental autoimmune encephalomyelitis (EAE) during adolescence and early young adulthood, while an increase in immunological tolerance with aging suppresses disease onset after late young adulthood in mice. Furthermore, gut dysbiosis induces the expression of complement C3 and production of the anaphylatoxin C3a, and down-regulates the expression of the

Indexed as

AnimalsAutoimmunityCentral Nervous SystemComplement C3aDown-RegulationDysbiosisEncephalomyelitis, Autoimmune, ExperimentalForkhead Transcription FactorsGastrointestinal MicrobiomeGenes, MHC Class IIHLA-DR2 AntigenHumansImmune ToleranceMiceMice, TransgenicMultiple SclerosisComplement C3aForkhead Transcription FactorsHLA-DR2 AntigenReceptors, Antigen, T-CellUbiquitin-Protein Ligasesagingcomplementdysbiosisimmune tolerancemultiple sclerosis

Identifiers

PMID29078267
PMCPMC5676872
OpenAlexW2767067645

What OpenQuestion holds

Textmetadata
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Registered trials

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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.