[HTML][HTML] Increase of CSF inflammatory profile in a case of highly active multiple sclerosis

R Magliozzi, D Marastoni, S Rossi, M Castellaro… - BMC neurology, 2019 - Springer
R Magliozzi, D Marastoni, S Rossi, M Castellaro, V Mazziotti, M Pitteri, A Gajofatto
BMC neurology, 2019Springer
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 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 …
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
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
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.
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