Evidence map›Paper›PMID 39201609›Full record

ArticleInternational journal of molecular sciences2024

Disclosing the Novel Protective Mechanisms of Ocrelizumab in Multiple Sclerosis: The Role of PKC Beta and Its Down-Stream Targets.

Lucrezia Irene Maria Campagnoli, Lara Ahmad, Nicoletta Marchesi, Giacomo Greco, Federica Boschi, Francesco Masi, Giulia Mallucci, Roberto Bergamaschi, Elena Colombo, Alessia Pascale

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Sex- and age-specific associations ofAnnals of medicine · 2026
    Article
  2. 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

10 authors.

Lucrezia Irene Maria CampagnoliDepartment of Drug Sciences, Section of Pharmacology, University of Pavia, 27100 Pavia, Italy.ORCID 0000-0001-6680-216X
Lara AhmadMultiple Sclerosis Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0003-2463-6815
Nicoletta MarchesiDepartment of Drug Sciences, Section of Pharmacology, University of Pavia, 27100 Pavia, Italy.ORCID 0000-0001-6271-1420
Giacomo GrecoMultiple Sclerosis Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0001-8097-0565
Federica BoschiDepartment of Drug Sciences, Section of Pharmacology, University of Pavia, 27100 Pavia, Italy.ORCID 0000-0002-3192-6397
Francesco MasiMultiple Sclerosis Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0009-0000-7048-6307
Giulia MallucciMultiple Sclerosis Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-0031-9594
Roberto BergamaschiMultiple Sclerosis Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-1397-511X
Elena ColomboMultiple Sclerosis Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-5265-5055
Alessia PascaleDepartment of Drug Sciences, Section of Pharmacology, University of Pavia, 27100 Pavia, Italy.ORCID 0000-0002-7182-4272

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ocrelizumab (OCR) is a humanized anti-CD20 monoclonal antibody approved for both Relapsing and Primary Progressive forms of Multiple Sclerosis (MS) treatment. OCR is postulated to act via rapid B cell depletion; however, by analogy with other anti-CD20 agents, additional effects can be envisaged, such as on Protein Kinase C (PKC). Hence, this work aims to explore novel potential mechanisms of action of OCR in peripheral blood mononuclear cells from MS patients before and after 12 months of OCR treatment. We first assessed, up-stream, PKCβII and subsequently explored two down-stream pathways: hypoxia-inducible factor 1 alpha (HIF-1α)/vascular endothelial growth factor (VEGF), and human antigen R (HuR)/manganese-dependent superoxide dismutase (MnSOD) and heat shock proteins 70 (HSP70). At baseline, higher levels of PKCβII, HIF-1α, and VEGF were found in MS patients compared to healthy controls (HC); interestingly, the overexpression of this inflammatory cascade was counteracted by OCR treatment. Conversely, at baseline, the content of HuR, MnSOD, and HSP70 was significantly lower in MS patients compared to HC, while OCR administration induced the up-regulation of these neuroprotective pathways. These results enable us to disclose the dual positive action of OCR: anti-inflammatory and neuroprotective. Therefore, in addition to B cell depletion, the effect of OCR on these molecular cascades can contribute to counteracting disease progression.

Indexed as

Antibodies, Monoclonal, HumanizedMultiple SclerosisProtein Kinase C betaAdultFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitLeukocytes, MononuclearMaleMiddle AgedSuperoxide DismutaseVascular Endothelial Growth Factor AAntibodies, Monoclonal, HumanizedHypoxia-Inducible Factor 1, alpha SubunitocrelizumabProtein Kinase C betaSuperoxide DismutaseVascular Endothelial Growth Factor AVEGFA protein, humanHIF-1αHSP70HuRMnSODmultiple sclerosisocrelizumabprotein kinase CVEGF

Identifiers

PMID39201609
PMCPMC11354964

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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.