Evidence map›Paper›PMID 42103467›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2026

Predictors of B-cell repopulation in people with multiple sclerosis treated with ocrelizumab: insights from two large cohorts.

Laura Hogenboom, Antonia McLean, Lisa Schoof, Lisa Taylor, Eva M Strijbis, Joep Killestein, Zoé L E van Kempen, Tomas Kalincik, Izanne Roos

Abstract readMulticenter Study
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

9 authors.

Laura HogenboomMS Center Amsterdam, Amsterdam UMC Location VUmc, Amsterdam, The Netherlands.ORCID http://orcid.org/0009-0005-1230-1366
Antonia McLeanNeuroimmunology Centre, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-0864-3057
Lisa SchoofMS Center Amsterdam, Amsterdam UMC Location VUmc, Amsterdam, The Netherlands.ORCID http://orcid.org/0009-0005-9845-5031
Lisa TaylorNeuroimmunology Centre, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Eva M StrijbisMS Center Amsterdam, Amsterdam UMC Location VUmc, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-6705-5864
Joep KillesteinMS Center Amsterdam, Amsterdam UMC Location VUmc, Amsterdam, The Netherlands.
Zoé L E van KempenMS Center Amsterdam, Amsterdam UMC Location VUmc, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9557-5381
Tomas KalincikNeuroimmunology Centre, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0003-3778-1376
Izanne RoosNeuroimmunology Centre, The Royal Melbourne Hospital, Melbourne, Victoria, Australia i.roos@unimelb.edu.au.ORCID http://orcid.org/0000-0003-0371-3666

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence indicates that B-cell dynamics during ocrelizumab treatment vary among individuals with multiple sclerosis. However, our understanding of B-cell dynamics is incomplete. We aim to characterise temporal profiles of CD19+ B-cell repopulation and identify demographic and clinical predictors of B-cell dynamics.

methodsThis was a retrospective multicentre cohort study including people with multiple sclerosis treated with ocrelizumab for ≥180 days from two academic centres. Variables of interest were visualised to explore their associations with CD19+ B-cell count. Generalised linear mixed effect models and logistic mixed effect models were used to identify predictors of CD19+ B-cell counts and early B-cell repopulation (>0.01×10

results567 participants, contributing 4592 CD19+ B-cell counts, were included. Younger age (β=-0.01, 95% CI -0.02 to -0.003), heavier weight (β=0.02, 95% CI 0.008 to 0.02), fewer ocrelizumab infusions (β=-0.07, 95% CI -0.08 to -0.06) and higher pre-ocrelizumab CD19+ B-cell counts (β=1.42, 95% CI 0.82 to 2.03) were associated with higher CD19+ B-cells during treatment. Pre-ocrelizumab CD19+ B-cells were higher in patients previously treated with natalizumab (mean B-cell count 0.57×10

conclusionsAge, weight, cumulative ocrelizumab exposure, pre-ocrelizumab CD19+ B-cell count and prior disease modifying therapy influence CD19+ B-cell repopulation during ocrelizumab treatment. With further elucidation of the association between B-cell dynamics and treatment effectiveness, these findings will help guide dosing of anti-CD20 therapies in the future.

Indexed as

Antibodies, Monoclonal, HumanizedB-LymphocytesImmunologic FactorsMultiple SclerosisAdultAntigens, CD19Cohort StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesAntibodies, Monoclonal, HumanizedAntigens, CD19Immunologic FactorsocrelizumabDEMYELINATING DISEASESIMMUNOLOGYMULTIPLE SCLEROSISPHARMACOKINETICS

Identifiers

PMID42103467
PMCPMC13479697

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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.