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

BACKGROUND: Evidence 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. METHODS: cells/L, 150-210 days post infusion). We have explored the patterns of early B-cell repopulation and relapse incidence within these groups. RESULTS: cells/L (IQR=0.02-0.13)). Early B-cell repopulation was more likely in patients with prior early repopulation (OR=3.00, 95% CI 1.61 to 5.61). Relapse incidence did not differ between the four patterns of B-cell repopulation dynamics. CONCLUSIONS: Age, 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.

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Publication Details

Journal
PubMed
Published
2026-05-08
DOI
https://doi.org/10.1136/jnnp-2026-338533
Primary Topic
Multiple Sclerosis Research Studies
Type
article
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article

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

Antonia McLean, Izanne Roos, Laura Hogenboom, Joep Killestein et al.
PubMed
Multiple Sclerosis Research Studies
article

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

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

Abstract

BACKGROUND: Evidence 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. METHODS: cells/L, 150-210 days post infusion). We have explored the patterns of early B-cell repopulation and relapse incidence within these groups. RESULTS: cells/L (IQR=0.02-0.13)). Early B-cell repopulation was more likely in patients with prior early repopulation (OR=3.00, 95% CI 1.61 to 5.61). Relapse incidence did not differ between the four patterns of B-cell repopulation dynamics. CONCLUSIONS: Age, 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.

PubMed
The Royal Melbourne Hospital (AU), Victorian Curriculum and Assessment Authority (AU), Victorian Comprehensive Cancer Centre (AU), Amsterdam Neuroscience (NL), Amsterdam University Medical Centers (NL), Victoria University (AU)
Good health and well-being
Openalex Percentile: Top 6%
Multiple Sclerosis Research Studies
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