Evidence map›Paper›PMID 35652942›Full record

ArticleJournal of neurology2022

Early B cells repopulation in multiple sclerosis patients treated with rituximab is not predictive of a risk of relapse or clinical progression.

Guillaume Dorcet, Hugo Migné, Damien Biotti, Chloé Bost, Fleur Lerebours, Jonathan Ciron, Emmanuel Treiner

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Review
  3. Ofatumumab in pediatric multiple sclerosis: a case series.Therapeutic advances in neurological disorders · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Assessing Sustained B-Cell Depletion and Disease Activity in a French Multiple Sclerosis Cohort Treated by Long-Term IV Anti-CD20 Antibody Therapy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  9. Article
  10. 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

7 authors at 2 institutions in 1 country.

Guillaume Dorcet *Department of Neurology, CRC-SEP, University Hospital of Toulouse, Toulouse, France.
Hugo Migné *Immunology Laboratory, Biology Department, University Hospital of Toulouse, Toulouse, France.
Damien BiottiDepartment of Neurology, CRC-SEP, University Hospital of Toulouse, Toulouse, France.
Chloé BostINSERM U1291-CNRS 5051, INFINITy, Toulouse, France.
Fleur LereboursDepartment of Neurology, CRC-SEP, University Hospital of Toulouse, Toulouse, France.
Jonathan CironDepartment of Neurology, CRC-SEP, University Hospital of Toulouse, Toulouse, France.
Emmanuel TreinerINSERM U1291-CNRS 5051, INFINITy, Toulouse, France. treiner.e@chu-toulouse.fr.ORCID http://orcid.org/0000-0001-6249-4534
Centre National de la Recherche Scientifique · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt is currently unknown whether early B cell reconstitution (EBR) in MS patients under rituximab is associated with a risk of relapse or progression.

objectivesAnalyzing EBR in rituximab-treated patients and its putative association with clinical findings.

methodsProspective lymphocytes immunophenotyping was performed in a monocentric cohort of MS patients treated by rituximab for 2 years. EBR was defined when B cells concentration was > 5 cells/mm3. B cell subsets were retrospectively associated with clinical data. Clinical and radiological monitoring included relapses, EDSS (Expanded Disability Status Scale), SDMT (Symbol Digit Modalities Test), and MRI.

results182 patients were analyzed (61 remitting-relapsing and 121 progressive-active). 38.5% experienced EBR at least once, but very few (7/182) showed systematic reconstitution. Most patients remained stable upon treatment, regardless of the occurrence of EBR. Dynamics of B cell reconstitution featured increased naïve/transitional B cells, and decreased memory subsets. Homeostasis of the B cell compartment differed at baseline between patients experiencing or not EBR upon treatment. In patients with EBR, reciprocal dynamics of transitional and pro-inflammatory double-negative B cell subsets was associated with better response to rituximab treatment.

conclusionEBR is common in rituximab-treated MS patients and is not associated with clinical disease activity. EBR in the peripheral blood may reflect regulatory immunological phenomena in subgroup of patients.

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingChronic DiseaseHumansProspective StudiesRecurrenceRetrospective StudiesRituximabRituximabB cellsImmunophenotypingMonitoring-B cell reconstitutionMultiple sclerosisRituximab

Identifiers

PMID35652942
PMCPMC9159933
OpenAlexW4281795292

What OpenQuestion holds

Textmetadata
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.