Evidence map›Paper›PMID 42133543›Full record

ArticleBrain and behavior2026

The Effect of Ocrelizumab on Anti-JC Virus Antibody Index.

Akash Virupakshaiah, Alexander J Gill, Vinicius A Schoeps, Emma Wilson, James Wilson, David Do, Amit Bar-Or, Dina Jacobs, Joseph R Berger

Abstract read
In one paragraph

Article in Brain and behavior, 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. 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

9 authors.

Akash VirupakshaiahDepartment of Neurology, University of California San Francisco, San Francisco, California, USA.ORCID https://orcid.org/0000-0003-2624-9974
Alexander J GillDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Vinicius A SchoepsDepartment of Neurology, University of California San Francisco, San Francisco, California, USA.ORCID https://orcid.org/0000-0001-8875-0567
Emma WilsonDepartment of Neurology, Penn Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
James WilsonDepartment of Neurology, Penn Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
David DoDepartment of Neurology, Penn Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Amit Bar-OrDepartment of Neurology, Penn Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Dina JacobsDepartment of Neurology, Penn Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Joseph R BergerDepartment of Neurology, Penn Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Funding

Roche/Genentech
6 · The paper itself

Abstract

PURPOSE/

introductionThe anti-JC virus (JCV) antibody index is used to stratify the risk of progressive multifocal leukoencephalopathy (PML) in multiple sclerosis (MS), particularly with natalizumab therapy. B-cell-depleting therapies may alter antibody levels and potentially confound the estimation of PML risk. This study evaluated the effect of ocrelizumab on anti-JCV antibody indices during the first 2 years of treatment.

methodsWe conducted a retrospective cohort study of 553 MS patients who initiated ocrelizumab between 2017 and 2019. Anti-JCV antibody indices were measured using the STRATIFY JCV assay at baseline and approximately every 6 months prior to subsequent infusions. Linear mixed-effects models were used to assess longitudinal changes in log-transformed JCV indices, adjusting for age, sex, and ethnicity. Secondary analyses evaluated serum B-cell counts and immunoglobulin levels. Sensitivity analyses addressed missing data. RESULTS/FINDING: There was no significant change in anti-JCV antibody index over time following ocrelizumab initiation (mean percent change per infusion cycle -0.049%, 95% CI: -0.449 to 0.351; p = 0.81). Results were consistent across sensitivity analyses and did not differ by age or sex. In contrast, peripheral B-cell counts declined significantly after treatment initiation and remained suppressed. Serum IgG, IgM, and IgA levels decreased modestly but significantly over time. JCV seroconversion occurred in 4.1% of initially seronegative patients, while seroreversion occurred in 6.6% of initially seropositive patients.

conclusionAnti-JCV antibody indices remain stable during the first 2 years of ocrelizumab treatment despite marked B-cell depletion and modest reductions in serum immunoglobulins. These findings suggest that existing PML risk stratification tools based on anti-JCV antibody indices remain applicable during early ocrelizumab therapy.

Indexed as

Antibodies, Monoclonal, HumanizedAntibodies, ViralImmunologic FactorsJC VirusLeukoencephalopathy, Progressive MultifocalMultiple SclerosisAdultB-LymphocytesFemaleHumansMaleMiddle AgedRetrospective StudiesAntibodies, Monoclonal, HumanizedAntibodies, ViralImmunologic FactorsocrelizumabimmunoglobulinsJC virus antibodiesmultiple sclerosisocrelizumabprogressive multifocal leukoencephalopathy

Identifiers

PMID42133543
PMCPMC13175193

What OpenQuestion holds

Textmetadata
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.