Background: The role of vaccine-mediated inflammation in exacerbating multiple sclerosis (MS) is a matter of debate. Objective: In this cross-sectional study, we compared the cerebrospinal fluid (CSF) inflammation associated with MS relapses or anti-COVID-19 mRNA vaccinations in relapsing-remitting multiple sclerosis (RRMS). Methods: We dosed CSF cytokines in 97 unvaccinated RRMS patients with clinical relapse within the last 100 days. In addition, we enrolled 29 stable RRMS and 24 control patients receiving COVID-19 vaccine within the last 100 days. Results: In RRMS patients, a negative association was found between relapse distance and the CSF concentrations of the pro-inflammatory cytokines interleukin (IL)-2 (beta = -0.265, p = 0.016), IL-6 (beta = -0.284, p = 0.01), and IL-17 (beta = -0.224, p = 0.044). Conversely, vaccine distance positively correlated with a different set of cytokines including IL-12 (beta = 0.576, p = 0.002), IL-13 (beta = 0.432, p = 0.027), and IL-1ra (beta = 0.387, p = 0.05). These associations were significant also considering other clinical characteristics. No significant associations emerged between vaccine distance and CSF molecules in the control group. Conclusion: Vaccine for COVID-19 induces a central inflammatory response in RRMS patients that is qualitatively different from that associated with disease relapse.

Bruno, A., Buttari, F., Dolcetti, E., Azzolini, F., Borrelli, A., Lauritano, G., et al. (2023). Distinct intrathecal inflammatory signatures following relapse and anti-COVID-19 mRNA vaccination in multiple sclerosis. MULTIPLE SCLEROSIS, 29(11-12), 1383-1392 [10.1177/13524585231197928].

Distinct intrathecal inflammatory signatures following relapse and anti-COVID-19 mRNA vaccination in multiple sclerosis

Bruno, Antonio;Buttari, Fabio;Dolcetti, Ettore;Lauritano, Gianluca;Di Caprio, Veronica;Rizzo, Francesca Romana;Gilio, Luana;Guadalupi, Livia;Musella, Alessandra;Centonze, Diego;
2023-09-12

Abstract

Background: The role of vaccine-mediated inflammation in exacerbating multiple sclerosis (MS) is a matter of debate. Objective: In this cross-sectional study, we compared the cerebrospinal fluid (CSF) inflammation associated with MS relapses or anti-COVID-19 mRNA vaccinations in relapsing-remitting multiple sclerosis (RRMS). Methods: We dosed CSF cytokines in 97 unvaccinated RRMS patients with clinical relapse within the last 100 days. In addition, we enrolled 29 stable RRMS and 24 control patients receiving COVID-19 vaccine within the last 100 days. Results: In RRMS patients, a negative association was found between relapse distance and the CSF concentrations of the pro-inflammatory cytokines interleukin (IL)-2 (beta = -0.265, p = 0.016), IL-6 (beta = -0.284, p = 0.01), and IL-17 (beta = -0.224, p = 0.044). Conversely, vaccine distance positively correlated with a different set of cytokines including IL-12 (beta = 0.576, p = 0.002), IL-13 (beta = 0.432, p = 0.027), and IL-1ra (beta = 0.387, p = 0.05). These associations were significant also considering other clinical characteristics. No significant associations emerged between vaccine distance and CSF molecules in the control group. Conclusion: Vaccine for COVID-19 induces a central inflammatory response in RRMS patients that is qualitatively different from that associated with disease relapse.
12-set-2023
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/26
Settore BIO/13
Settore MEDS-12/A - Neurologia
English
CSF
MS
cytokines
neuroinflammation
relapse
vaccine
Bruno, A., Buttari, F., Dolcetti, E., Azzolini, F., Borrelli, A., Lauritano, G., et al. (2023). Distinct intrathecal inflammatory signatures following relapse and anti-COVID-19 mRNA vaccination in multiple sclerosis. MULTIPLE SCLEROSIS, 29(11-12), 1383-1392 [10.1177/13524585231197928].
Bruno, A; Buttari, F; Dolcetti, E; Azzolini, F; Borrelli, A; Lauritano, G; Di Caprio, V; Rizzo, Fr; Gilio, L; Galifi, G; Furlan, R; Finardi, A; Guadal...espandi
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/341667
Citazioni
  • ???jsp.display-item.citation.pmc??? 2
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 2
social impact