Evidence map›Paper›PMID 39819054›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2025

Alterations in Gut Microbiome-Host Relationships After Immune Perturbation in Patients With Multiple Sclerosis.

Vinod K Gupta, Guneet S Janda, Heather K Pump, Nikhil Lele, Isabella Cruz, Inessa Cohen, William E Ruff, David A Hafler, Jaeyun Sung, Erin E Longbrake

Abstract read
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Female-enrichedbioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
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  11. Immune perturbation by the ileal microbiota in multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
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

10 authors.

Vinod K GuptaMicrobiomics Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0003-1467-9993
Guneet S JandaYale School of Medicine Department of Neurology, New Haven, CT.
Heather K PumpMayo Clinic Alix School of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0003-2448-9712
Nikhil LeleYale School of Medicine Department of Neurology, New Haven, CT.ORCID 0000-0001-7367-1364
Isabella CruzYale School of Medicine Department of Neurology, New Haven, CT.
Inessa CohenYale School of Medicine Department of Neurology, New Haven, CT.ORCID 0000-0002-5807-2635
William E RuffYale School of Medicine Department of Neurology, New Haven, CT.
David A HaflerYale School of Medicine Department of Neurology, New Haven, CT.ORCID 0000-0003-4664-535X
Jaeyun SungMicrobiomics Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN.
Erin E LongbrakeYale School of Medicine Department of Neurology, New Haven, CT.ORCID 0000-0002-1179-3937

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesGut microbial symbionts have been shown to influence the development of autoimmunity in multiple sclerosis (MS). Emerging research points to an important relationship between the microbial-IgA interface and MS pathophysiology. IgA-secreting B cells are observed in the MS brain, and shifts in gut bacteria-IgA binding have been described in some patients with MS. However, the relationships between the gut microbiome and the host immune response, particularly regarding B-cell-depleting immunomodulation, remain underexplored. This study aimed to evaluate the composition of the gut microbiome in patients with newly diagnosed MS at baseline and after B-cell depletion, using long-read sequencing for enhanced taxonomic resolution. We further aimed to investigate the host/microbiome interface by evaluating microbe/immunoglobulin A relationships.

methodsWe collected stool samples from 43 patients with newly diagnosed, untreated MS and 42 matched healthy controls. Nineteen patients with MS initiated anti-CD20 monoclonal antibody treatment and donated additional stool samples after 6 months of treatment. We evaluated the host-microbial interface using bacterial flow cytometry and long-read 16S rRNA gene amplicon sequencing. We used Immune Coating Scores to compare the proportions of bacteria identified in the IgA-coated vs IgA-uncoated bacterial fractions.

resultsPatients with untreated, newly diagnosed MS showed significant reductions in IgA-bound fecal microbiota compared with controls. Using multiple linear regression models adjusted for potential confounders, we observed significant ( DISCUSSION: This analysis of gut microbial ASVs reveals shifts in taxonomic strains induced by immune modulation in MS.

Indexed as

Gastrointestinal MicrobiomeHost Microbial InteractionsMultiple SclerosisAdultFecesFemaleHumansImmunoglobulin AMaleMiddle AgedImmunoglobulin A

Identifiers

PMID39819054
PMCPMC11741292

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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.