High anti-JCPyV serum titers coincide with high CSF cell counts in RRMS patients.

CSF cell counts JCPyV JCV index Multiple sclerosis cerebrospinal fluid clinical activity natalizumab progressive multifocal leukoencephalopathy tissue-resident memory cells

Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
09 2021
Historique:
pubmed: 6 11 2020
medline: 25 2 2023
entrez: 5 11 2020
Statut: ppublish

Résumé

Progressive multifocal leukoencephalopathy (PML) can in rare cases occur in natalizumab-treated patients with high serum anti-JCPyV antibodies, hypothetically due to excessive blockade of immune cell migration. Immune cell recruitment to the central nervous system (CNS) was assessed in relapsing-remitting multiple sclerosis (RRMS) patients stratified by low versus high anti-JCPyV antibody titers as indicator for PML risk. Cerebrospinal fluid (CSF) cell counts of 145 RRMS patients were quantified by flow cytometry. Generalized linear models were employed to assess influence of age, sex, disease duration, Expanded Disability Status Scale (EDSS), clinical/radiological activity, current steroid or natalizumab treatment, as well as anti-JCPyV serology on CSF cell subset counts. While clinical/radiological activity was associated with increased CD4, natural killer (NK), B and plasma cell counts, natalizumab therapy reduced all subpopulations except monocytes. With and without natalizumab therapy, patients with high anti-JCPyV serum titers presented with increased CSF T-cell counts compared to patients with low anti-JCPyV serum titers. In contrast, PML patients assessed before ( High anti-JCPyV indices, which could be indicative of increased viral activity, are associated with elevated immune cell recruitment to the CNS. Its excessive impairment in conjunction with viral activity could predispose for PML development.

Sections du résumé

BACKGROUND
Progressive multifocal leukoencephalopathy (PML) can in rare cases occur in natalizumab-treated patients with high serum anti-JCPyV antibodies, hypothetically due to excessive blockade of immune cell migration.
OBJECTIVE
Immune cell recruitment to the central nervous system (CNS) was assessed in relapsing-remitting multiple sclerosis (RRMS) patients stratified by low versus high anti-JCPyV antibody titers as indicator for PML risk.
METHODS
Cerebrospinal fluid (CSF) cell counts of 145 RRMS patients were quantified by flow cytometry. Generalized linear models were employed to assess influence of age, sex, disease duration, Expanded Disability Status Scale (EDSS), clinical/radiological activity, current steroid or natalizumab treatment, as well as anti-JCPyV serology on CSF cell subset counts.
RESULTS
While clinical/radiological activity was associated with increased CD4, natural killer (NK), B and plasma cell counts, natalizumab therapy reduced all subpopulations except monocytes. With and without natalizumab therapy, patients with high anti-JCPyV serum titers presented with increased CSF T-cell counts compared to patients with low anti-JCPyV serum titers. In contrast, PML patients assessed before (
CONCLUSION
High anti-JCPyV indices, which could be indicative of increased viral activity, are associated with elevated immune cell recruitment to the CNS. Its excessive impairment in conjunction with viral activity could predispose for PML development.

Identifiants

pubmed: 33150829
doi: 10.1177/1352458520970103
pmc: PMC8414828
doi:

Substances chimiques

Natalizumab 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1491-1496

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Auteurs

Tilman Schneider-Hohendorf (T)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Andreas Schulte-Mecklenbeck (A)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Patrick Ostkamp (P)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Claudia Janoschka (C)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Marc Pawlitzki (M)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Felix Luessi (F)

Department of Neurology, Focus Program Translational Neuroscience (FTN) and Immunotherapy (FZI), Rhine Main Neuroscience Network (rmn), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Frauke Zipp (F)

Department of Neurology, Focus Program Translational Neuroscience (FTN) and Immunotherapy (FZI), Rhine Main Neuroscience Network (rmn), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Sven G Meuth (SG)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Luisa Klotz (L)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Heinz Wiendl (H)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Catharina C Gross (CC)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Nicholas Schwab (N)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

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