Evidence map›Paper›PMID 41373455›Full record

ArticleInternational journal of molecular sciences2025

Assessing Peripheral Blood Biomarkers and Predictive Patterns in Multiple Sclerosis Using Cytokines and Immune Gene Expression Profiles in Ocrelizumab-Treated Patients: Tracking Tumor Necrosis Factor.

Bojan Jevtić, Nikola Momcilovic, Goran Stegnjaić, Milica Lazarević, Suzana Stanisavljević, Olivera Tamas, Nikola Veselinovic, Maja Budimkic, Sarlota Mesaros, Đorđe Miljković and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. Review
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

13 authors.

Bojan JevtićDepartment of Immunology, Institute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11060 Belgrade, Serbia.ORCID 0000-0002-1076-0543
Nikola MomcilovicClinic of Neurology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.
Goran StegnjaićDepartment of Immunology, Institute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11060 Belgrade, Serbia.
Milica LazarevićDepartment of Immunology, Institute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11060 Belgrade, Serbia.
Suzana StanisavljevićDepartment of Immunology, Institute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11060 Belgrade, Serbia.ORCID 0000-0003-0781-8828
Olivera TamasClinic of Neurology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.ORCID 0009-0006-9924-0734
Nikola VeselinovicClinic of Neurology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.
Maja BudimkicClinic of Neurology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.
Sarlota MesarosClinic of Neurology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.
Đorđe MiljkovićDepartment of Immunology, Institute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11060 Belgrade, Serbia.ORCID 0000-0002-5613-9306
Tatjana PekmezovicFaculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0001-7978-1409
Jelena DrulovicClinic of Neurology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.ORCID 0000-0002-4516-3458
Neda NikolovskiDepartment of Immunology, Institute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11060 Belgrade, Serbia.

Funding

Wellcome Trust 200110
6 · The paper itself

Abstract

Ocrelizumab, a humanized monoclonal anti-CD20 and B cell-depleting antibody, is a disease-modifying therapy for multiple sclerosis (MS), a chronic inflammatory, demyelinating, and neurodegenerative disease of the central nervous system. However, reliable predictive biomarkers of ocrelizumab's effectiveness, such as cytokine expression profiles in peripheral blood mononuclear cells (PBMCs), are lacking. The aim of this study was to identify immunological biomarkers of ocrelizumab treatment response in MS patients, during a two-year follow-up. mRNA expression for specific immune molecules in PBMCs was measured, and consequently correlated with the clinical and radiological parameters of disease activity. PBMCs were obtained from 80 MS patients (35 with relapsing-remitting MS-RRMS and 45 with primary progressive-PPMS), immediately before initiating ocrelizumab treatment and thereafter every 6 months (before the administration of the next dose of ocrelizumab). Expression of the B cell marker

Indexed as

Antibodies, Monoclonal, HumanizedBiomarkersCytokinesMultiple SclerosisMultiple Sclerosis, Relapsing-RemittingTumor Necrosis Factor-alphaAdultFemaleHumansLeukocytes, MononuclearMaleMiddle AgedTranscriptomeAntibodies, Monoclonal, HumanizedBiomarkersCytokinesocrelizumabTumor Necrosis Factor-alphaB cellsbiomarkermultiple sclerosisocrelizumabTNF

Identifiers

PMID41373455
PMCPMC12691730

What Socratic holds

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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 Socratic graph.