Evidence map›Paper›PMID 28893978›Full record

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

Gut bacteria from multiple sclerosis patients modulate human T cells and exacerbate symptoms in mouse models.

Egle Cekanaviciute, Bryan B Yoo, Tessel F Runia, Justine W Debelius, Sneha Singh, Charlotte A Nelson, Rachel Kanner, Yadira Bencosme, Yun Kyung Lee, Stephen L Hauser and 9 more

Erratum issued 4 registry-linked trialsOpen 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. An erratum has been issued. It is linked to 4 registered trials, which are not on this map. Cited by 602 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
602citing papers in PubMed, 7 pooled it
34.7field-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.

NCT03594487 phase1terminatednot on this mapstarted 2018, after this paper: background citation

Fecal Microbiota Transplantation (FMT) of FMP30 in Relapsing-Remitting Multiple Sclerosis: A Phase 1b Clinical Trial to Evaluate Feasibility, Safety, Tolerability and Effects on Immune Function

TypeinterventionalSponsorJeffrey GelfandRan2018 to 2024Enrolled5ConditionsRelapsing Remitting Multiple SclerosisArmsFMP30 Donor Stool, Fecal Microbiota Transplantation (FMT) of FMP30 Donor Stool, Observational Control
NCT03975413 completednot on this mapstarted 2018, after this paper: background citation

Single-Arm, Non-Randomized, Time Series, Single-Subject Study: Fecal Microbiota Transplantation (FMT) in Multiple Sclerosis

TypeobservationalSponsorRush University Medical CenterRan2018 to 2020Enrolled1ConditionsMultiple Sclerosis, Relapsing-RemittingArmsFecal Microbiota Transplantation (FMT)
NCT05081700 completednot on this mapstarted 2020, after this paper: background citation

A Systems Approach to Understanding Disease Processes in Multiple Sclerosis

TypeobservationalSponsorProvidence Health & ServicesRan2020 to 2023Enrolled14ConditionsMultiple SclerosisArmsAll patients in the study will be treated with ocrelizumab
NCT05808101 terminatednot on this mapstarted 2022, after this paper: background citation

Role of the Gut Microbiome as Determinant of Depression in Multiple Sclerosis Subjects

TypeobservationalSponsorWashington University School of MedicineRan2022 to 2024Enrolled51ConditionsMultiple Sclerosis, DepressionArmsNeuro-QoL T-score determination
3 · Its place in the literature

Who cites it

602 citing papers in PubMed, 7 syntheses or guidelines pooled it, 1,035 citations in OpenAlex.

  1. Pooled it
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  7. International journal of molecular sciences · 2024
    Pooled it
  8. Trial
  9. Article
  10. Article
  11. Article
  12. Review
  13. The Gut Microbiome in Multiple Sclerosis.Neurology(R) neuroimmunology & neuroinflammation · 2026
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

542 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 1 country.

Egle CekanaviciuteDepartment of Neurology, University of California, San Francisco, CA 94158.
Bryan B YooDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Tessel F RuniaDepartment of Neurology, University of California, San Francisco, CA 94158.
Justine W DebeliusCenter for Microbiome Innovation, University of California, San Diego, La Jolla, CA 92093.
Sneha SinghDepartment of Neurology, University of California, San Francisco, CA 94158.
Charlotte A NelsonDepartment of Neurology, University of California, San Francisco, CA 94158.
Rachel KannerDepartment of Neurology, University of California, San Francisco, CA 94158.
Yadira BencosmeDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Yun Kyung LeeDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Stephen L HauserDepartment of Neurology, University of California, San Francisco, CA 94158.
Elizabeth Crabtree-HartmanDepartment of Neurology, University of California, San Francisco, CA 94158.
Ilana Katz SandDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Mar GaciasDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Yunjiao ZhuDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Patrizia CasacciaDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Bruce A C CreeDepartment of Neurology, University of California, San Francisco, CA 94158.
Rob KnightCenter for Microbiome Innovation, University of California, San Diego, La Jolla, CA 92093.
Sarkis K MazmanianDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Sergio E BaranziniDepartment of Neurology, University of California, San Francisco, CA 94158; sergio.baranzini@ucsf.edu.ORCID 0000-0003-0067-194X
University of California, San Francisco · USIcahn School of Medicine at Mount Sinai · USCalifornia Institute of Technology · USUniversity of California San Diego · USThe Graduate Center, CUNY · US

Funding

UCSF IRACDA Scholars ProgramK12GM081266 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Raymond M. Esquerra, HOLLY A. INGRAHAM · 2007 to 2026
$19.4M
BMI Bioinformatics Training GrantsT32GM067547 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, RYAN D. · 2003 to 2022
$6.6M
Histone Deacetylation in Oligodendrocyte DifferentiationR37NS042925 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CASACCIA, PATRIZIA · 2012 to 2018
$4.3M
NIGMS NIH HHS K12 GM081266NIGMS NIH HHS T32 GM067547NINDS NIH HHS R37 NS042925
6 · The paper itself

Abstract

The gut microbiota regulates T cell functions throughout the body. We hypothesized that intestinal bacteria impact the pathogenesis of multiple sclerosis (MS), an autoimmune disorder of the CNS and thus analyzed the microbiomes of 71 MS patients not undergoing treatment and 71 healthy controls. Although no major shifts in microbial community structure were found, we identified specific bacterial taxa that were significantly associated with MS.

Indexed as

Disease Models, AnimalGastrointestinal MicrobiomeAnimalsCells, CulturedEncephalomyelitis, Autoimmune, ExperimentalFemaleHumansLeukocytes, MononuclearMaleMiceMultiple SclerosisT-LymphocytesT-Lymphocytes, Regulatoryautoimmunitymicrobiomemultiple sclerosis

Identifiers

PMID28893978
PMCPMC5635915
OpenAlexW2750838281

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.