Cargando…

Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis

INTRODUCTION: Multiple sclerosis (MS) is a chronic inflammatory autoimmune demyelinating disease that secondarily leads to axonal loss and associated brain atrophy. Disease-modifying drugs (DMDs) have previously been studied for their ability to affect specific immunity. This study investigates the...

Descripción completa

Detalles Bibliográficos
Autores principales: Peterka, Marek, Valis, Martin, Soucek, Ondrej, Krejsek, Jan, Sobisek, Lukáš, Sejkorova, Ilona, Klimova, Blanka, Stourac, Pavel, Pavelek, Zbysek, Novotny, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623392/
https://www.ncbi.nlm.nih.gov/pubmed/37473734
http://dx.doi.org/10.1159/000532022
_version_ 1785130731691835392
author Peterka, Marek
Valis, Martin
Soucek, Ondrej
Krejsek, Jan
Sobisek, Lukáš
Sejkorova, Ilona
Klimova, Blanka
Stourac, Pavel
Pavelek, Zbysek
Novotny, Michal
author_facet Peterka, Marek
Valis, Martin
Soucek, Ondrej
Krejsek, Jan
Sobisek, Lukáš
Sejkorova, Ilona
Klimova, Blanka
Stourac, Pavel
Pavelek, Zbysek
Novotny, Michal
author_sort Peterka, Marek
collection PubMed
description INTRODUCTION: Multiple sclerosis (MS) is a chronic inflammatory autoimmune demyelinating disease that secondarily leads to axonal loss and associated brain atrophy. Disease-modifying drugs (DMDs) have previously been studied for their ability to affect specific immunity. This study investigates the effect of interferon beta-1a (INF) and glatiramer acetate (GA) administration on changes in innate immunity cell populations. METHODS: Sixty Caucasian female patients with relapsing-remitting MS undergo blood sample testing for 15 blood parameters at baseline, 1 month, 3 months, and 6 months after treatment by GA or IFN (started as their first-line DMD). RESULTS: A statistically significant difference in the change after 6 months was found in the parameter monocytes (relative count) in the group of patients treated with IFN. The median increase was 27.8%. Changes in many of the other 15 parameters studied were 10–20%. CONCLUSION: Innate immunity has long been neglected in MS immunopathology. The findings suggest that IFN treatment may modulate the immune response in MS by affecting monocyte function and may provide insight into the mechanisms of action of IFN in MS.
format Online
Article
Text
id pubmed-10623392
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher S. Karger AG
record_format MEDLINE/PubMed
spelling pubmed-106233922023-11-04 Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis Peterka, Marek Valis, Martin Soucek, Ondrej Krejsek, Jan Sobisek, Lukáš Sejkorova, Ilona Klimova, Blanka Stourac, Pavel Pavelek, Zbysek Novotny, Michal Eur Neurol Basic Investigative Studies: Research Article INTRODUCTION: Multiple sclerosis (MS) is a chronic inflammatory autoimmune demyelinating disease that secondarily leads to axonal loss and associated brain atrophy. Disease-modifying drugs (DMDs) have previously been studied for their ability to affect specific immunity. This study investigates the effect of interferon beta-1a (INF) and glatiramer acetate (GA) administration on changes in innate immunity cell populations. METHODS: Sixty Caucasian female patients with relapsing-remitting MS undergo blood sample testing for 15 blood parameters at baseline, 1 month, 3 months, and 6 months after treatment by GA or IFN (started as their first-line DMD). RESULTS: A statistically significant difference in the change after 6 months was found in the parameter monocytes (relative count) in the group of patients treated with IFN. The median increase was 27.8%. Changes in many of the other 15 parameters studied were 10–20%. CONCLUSION: Innate immunity has long been neglected in MS immunopathology. The findings suggest that IFN treatment may modulate the immune response in MS by affecting monocyte function and may provide insight into the mechanisms of action of IFN in MS. S. Karger AG 2023-07-20 2023-11 /pmc/articles/PMC10623392/ /pubmed/37473734 http://dx.doi.org/10.1159/000532022 Text en © 2023 S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Basic Investigative Studies: Research Article
Peterka, Marek
Valis, Martin
Soucek, Ondrej
Krejsek, Jan
Sobisek, Lukáš
Sejkorova, Ilona
Klimova, Blanka
Stourac, Pavel
Pavelek, Zbysek
Novotny, Michal
Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis
title Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis
title_full Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis
title_fullStr Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis
title_full_unstemmed Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis
title_short Interferon Beta-1a versus Glatiramer Acetate: Changes of Innate Immunity in a Group of Women with Multiple Sclerosis
title_sort interferon beta-1a versus glatiramer acetate: changes of innate immunity in a group of women with multiple sclerosis
topic Basic Investigative Studies: Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623392/
https://www.ncbi.nlm.nih.gov/pubmed/37473734
http://dx.doi.org/10.1159/000532022
work_keys_str_mv AT peterkamarek interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT valismartin interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT soucekondrej interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT krejsekjan interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT sobiseklukas interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT sejkorovailona interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT klimovablanka interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT stouracpavel interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT pavelekzbysek interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis
AT novotnymichal interferonbeta1aversusglatirameracetatechangesofinnateimmunityinagroupofwomenwithmultiplesclerosis