Evidence map›Paper›PMID 35260584›Full record

Observational studyScientific reports2022

B-cell-depletion reverses dysbiosis of the microbiome in multiple sclerosis patients.

Alba Troci, Olga Zimmermann, Daniela Esser, Paula Krampitz, Sandra May, Andre Franke, Daniela Berg, Frank Leypoldt, Klarissa Hanja Stürner, Corinna Bang

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
3.0field-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, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  17. Oral microbiota and central nervous system diseases: A review.Neuroprotection (Chichester, England) · 2025
    Review
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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

10 authors at 1 institution in 1 country.

Alba TrociInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Olga ZimmermannDepartment of Neurology, Kiel University, Arnold-Heller-Strasse 3, 24105, Kiel, Germany.
Daniela EsserInstitute of Clinical Chemistry UKSH Kiel/Lübeck, Kiel University, Kiel, Germany.
Paula KrampitzInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Sandra MayInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Andre FrankeInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Daniela BergDepartment of Neurology, Kiel University, Arnold-Heller-Strasse 3, 24105, Kiel, Germany.
Frank LeypoldtDepartment of Neurology, Kiel University, Arnold-Heller-Strasse 3, 24105, Kiel, Germany.
Klarissa Hanja Stürner *Department of Neurology, Kiel University, Arnold-Heller-Strasse 3, 24105, Kiel, Germany. k.stuerner@neurologie.uni-kiel.de.
Corinna Bang *Institute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Kiel University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To elucidate cross-sectional patterns and longitudinal changes of oral and stool microbiota in multiple sclerosis (MS) patients and the effect of B-cell depletion. We conducted an observational, longitudinal clinical cohort study analysing four timepoints over 12 months in 36 MS patients, of whom 22 initiated B-cell depleting therapy with ocrelizumab and a healthy control group. For microbiota analysis of the oral cavity and the gut, provided stool and oral swab samples underwent 16S rDNA sequencing and subsequent bioinformatic analyses. Oral microbiota-patterns exhibited a reduced alpha-diversity and unique differential microbiota changes compared to stool such as increased levels of Proteobacteria and decreased abundance of Actinobacteria. Following B-cell depletion, we observed increased alpha-diversity in the gut and the oral cavity as well as a long-term sustained reduction of pro-inflammatory Gram-negative bacteria (e.g., Escherichia/Shigella). MS patients have altered stool and oral microbiota diversity patterns compared to healthy controls, which are most pronounced in patients with higher disease activity and disability. Therapeutic B-cell depletion is associated with persisting regression of these changes. Whether these microbial changes are unspecific side-effects of B-cell depletion or indirectly modulate MS disease activity and progression is currently unknown and necessitates further investigations.

Indexed as

Gastrointestinal MicrobiomeMicrobiotaMultiple SclerosisCohort StudiesCross-Sectional StudiesDysbiosisFecesHumansRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID35260584
PMCPMC8904534
OpenAlexW4220780992

What OpenQuestion holds

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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.