Evidence map›Paper›PMID 41062789›Full record

ArticleNeurology and therapy2025

Selective S1P Receptor Modulation in Multiple Sclerosis Alters CXCL13:CXCR5-Associated Immune Activities Without Impacting Anti-SARS-CoV-2 Immunity.

Andrea Harrer, Richard F Radlberger, Beate Buchegger, Brooke Slade, Thomas Haybaeck, Hannes Oberkofler, Konstantin E Thiel, Ferdinand Otto, Tobias Moser, Peter Wipfler

Abstract read
In one paragraph

Article in Neurology and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Andrea Harrer *Department of Neurology, Christian-Doppler University Hospital, Paracelsus Medical University, Centre for Cognitive Neuroscience, EpiCARE, Salzburg, Austria. a.harrer@salk.at.ORCID http://orcid.org/0000-0001-7717-6125
Richard F Radlberger *Department of Neurology, Christian-Doppler University Hospital, Paracelsus Medical University, Centre for Cognitive Neuroscience, EpiCARE, Salzburg, Austria. r.radlberger@salk.at.ORCID http://orcid.org/0000-0002-5704-9097
Beate BucheggerDepartment of Dermatology and Allergology, Paracelsus Medical University, Salzburg, Austria.
Brooke SladeDepartment of Dermatology and Allergology, Paracelsus Medical University, Salzburg, Austria.
Thomas HaybaeckDepartment of Neurology, Christian-Doppler University Hospital, Paracelsus Medical University, Centre for Cognitive Neuroscience, EpiCARE, Salzburg, Austria.
Hannes OberkoflerDepartment of Laboratory Medicine, Paracelsus Medical University, Salzburg, Austria.
Konstantin E ThielCore Facility Biostatistics, Paracelsus Medical University, Salzburg, Austria.
Ferdinand OttoDepartment of Neurology, University Hospital, Zurich, Switzerland.
Tobias MoserDepartment of Neurology, Christian-Doppler University Hospital, Paracelsus Medical University, Centre for Cognitive Neuroscience, EpiCARE, Salzburg, Austria.
Peter WipflerDepartment of Neurology, Christian-Doppler University Hospital, Paracelsus Medical University, Centre for Cognitive Neuroscience, EpiCARE, Salzburg, Austria.

Funding

BMS, New York City, New York, Unites States of America BMS Protocol ID:IM047-036
6 · The paper itself

Abstract

introductionSphingosine-1-phosphate receptor (S1PR) modulators are effective therapies for multiple sclerosis (MS) that block lymphocyte egress from secondary lymphoid organs. This migration inhibition carries the risk of reduced infection-control as reported for the non-selective S1PR modulator, fingolimod. CXCL13:CXCR5-associated immune activities play a key role in protective antibody-based immunity but are also linked to inflammation in MS. Utilizing the ongoing SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) pandemic, we aimed to determine whether selective S1PR modulation with ozanimod acts on the CXCL13:CXCR5 axis for modulating MS activity and whether this impacts anti-viral immune responses.

methodsThis 1-year observational study included 20 patients with MS receiving ozanimod and 10 healthy probands. CXCR5

resultsCXCR5

conclusionSelective S1P receptor modulation with ozanimod affects the CXCL13:CXCR5 axis by reducing circulating CXCR5

Indexed as

CXCL13:CXCR5Multiple sclerosisOzanimodS1PR modulationSARS-CoV-2

Identifiers

PMID41062789
PMCPMC12623514

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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.