Increase of CSF inflammatory profile in a case of highly active multiple sclerosis.

Biomarkers CSF Chemokynes Cytokines Multiple sclerosis

Journal

BMC neurology
ISSN: 1471-2377
Titre abrégé: BMC Neurol
Pays: England
ID NLM: 100968555

Informations de publication

Date de publication:
26 Sep 2019
Historique:
received: 20 09 2018
accepted: 03 09 2019
entrez: 28 9 2019
pubmed: 29 9 2019
medline: 7 1 2020
Statut: epublish

Résumé

Clinical and imaging follow-up coupled with cerebrospinal fluid (CSF) and possibly serum profiling could provide information on disease activity and disability evolution in multiple sclerosis patients. We describe the case of a relapsing-remitting MS patient whose history was characterized by failure of several therapeutic approaches and sustained disease activity. By using a highly sensitive immunoassay methodology, we examined protein expression of 70 inflammatory/cytotoxic molecules in two consecutive paired CSF and serum samples, obtained respectively in 2006 and 2013. At disease diagnosis, elevated CSF protein levels of an inflammatory pattern, including CXCL13, CXCL12, IFNγ, TNF, sTNFR1, IL8, sCD163, APRIL, BAFF, pentraxin III and MMP2 were found compared with a group of controls. At the second lumbar puncture, sustained disease activity was accompanied by considerable (more than 2 fold changes) increase expression of most of these inflammatory molecules while no significant changes in serum inflammatory markers were detected in the two consecutive serum samples. Elevated CSF protein expression of pro-inflammatory mediators, possibly specifically associated to GM demyelination, could remain stable or increase over time in patients with active multiple sclerosis. We underline the role of fluid analysis in understanding the pathophysiology of the disease and providing information on possible markers of disease activity and evolution.

Sections du résumé

BACKGROUND BACKGROUND
Clinical and imaging follow-up coupled with cerebrospinal fluid (CSF) and possibly serum profiling could provide information on disease activity and disability evolution in multiple sclerosis patients.
CASE PRESENTATION METHODS
We describe the case of a relapsing-remitting MS patient whose history was characterized by failure of several therapeutic approaches and sustained disease activity. By using a highly sensitive immunoassay methodology, we examined protein expression of 70 inflammatory/cytotoxic molecules in two consecutive paired CSF and serum samples, obtained respectively in 2006 and 2013. At disease diagnosis, elevated CSF protein levels of an inflammatory pattern, including CXCL13, CXCL12, IFNγ, TNF, sTNFR1, IL8, sCD163, APRIL, BAFF, pentraxin III and MMP2 were found compared with a group of controls. At the second lumbar puncture, sustained disease activity was accompanied by considerable (more than 2 fold changes) increase expression of most of these inflammatory molecules while no significant changes in serum inflammatory markers were detected in the two consecutive serum samples.
CONCLUSIONS CONCLUSIONS
Elevated CSF protein expression of pro-inflammatory mediators, possibly specifically associated to GM demyelination, could remain stable or increase over time in patients with active multiple sclerosis. We underline the role of fluid analysis in understanding the pathophysiology of the disease and providing information on possible markers of disease activity and evolution.

Identifiants

pubmed: 31558148
doi: 10.1186/s12883-019-1455-7
pii: 10.1186/s12883-019-1455-7
pmc: PMC6764139
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

231

Subventions

Organisme : Italian Ministry of Health
ID : GR-2013-02-355322
Organisme : Fondazione Italiana Sclerosi Multipla
ID : FISM 16/17/F14

Références

Ann Neurol. 2005 Dec;58(6):840-6
pubmed: 16283615
Mult Scler. 2006 Dec;12(6):787-93
pubmed: 17263008
Ann Neurol. 2015 Jul;78(1):3-20
pubmed: 25808056
Nat Rev Neurol. 2015 Jul;11(7):379-89
pubmed: 26032396
Mult Scler. 2017 May;23(6):848-854
pubmed: 27527906
J Neuroinflammation. 2017 Feb 21;14(1):40
pubmed: 28222766
Ann Neurol. 2018 Apr;83(4):739-755
pubmed: 29518260
Neurology. 1983 Nov;33(11):1444-52
pubmed: 6685237

Auteurs

R Magliozzi (R)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy. rmagliozzi73@gmail.com.
Division of Brain Sciences, Department of Medicine, Imperial College London, London, UK. rmagliozzi73@gmail.com.

D Marastoni (D)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

S Rossi (S)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

M Castellaro (M)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.
Department of Information Engineering, University of Padova, Padova, Italy.

V Mazziotti (V)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

M Pitteri (M)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

A Gajofatto (A)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

S Monaco (S)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

M D Benedetti (MD)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

M Calabrese (M)

Neurology B, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico G.B. Rossi, P.le L.A. Scuro, 10, 37134, Verona, Italy.

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