TY - JOUR
T1 - A new serological autoantibody signature associated with multiple sclerosis
AU - Abdesselem, Houari
AU - de la Fuente, Alberto
AU - Bensmail, Ilham
AU - Elbashir, Israa E.
AU - Anuar, Diana
AU - Ti-Myen, Tan
AU - Abylova, Bermet
AU - Blackburn, Jonathan M.
AU - Malik, Rayaz A.
AU - Petropoulos, Ioannis N.
N1 - Publisher Copyright:
© 2025 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC license. http://creativecommons.org/licenses/by-nc/4.0/
PY - 2025/11
Y1 - 2025/11
N2 - The role of autoantibodies in the pathogenesis of Multiple Sclerosis (MS) remains incompletely understood. In this study, we analysed serum samples from a cohort of MS patients in Qatar using high-throughput KoRectly Expressed (KREX) immunome protein-array technology. Compared to healthy controls, MS patients showed significantly altered autoantibody responses to 129 proteins, with a notable enrichment in autoantibodies targeting antiviral immune response-related proteins and oligodendrocyte marker SOX-10. Machine learning analysis identified a distinct molecular signature comprising 17 differentially expressed autoantibodies, including those against MX1, ISG20, MAX, SUFU, NR1H2, HMGN5, and EPHA10. Among these, autoantibodies against MX1-a key effector in the interferon-alpha/beta signalling pathway-showed the most pronounced increase, with nearly a threefold elevation in MS patients. While MX1 has previously been implicated in MS, this is the first report of autoantibody reactivity against the protein, suggesting a potential role in disease onset and progression. These findings support a link between antiviral immune responses and MS pathophysiology and offer a promising blood-based autoantibody signature that could inform future diagnostic and therapeutic strategies.
AB - The role of autoantibodies in the pathogenesis of Multiple Sclerosis (MS) remains incompletely understood. In this study, we analysed serum samples from a cohort of MS patients in Qatar using high-throughput KoRectly Expressed (KREX) immunome protein-array technology. Compared to healthy controls, MS patients showed significantly altered autoantibody responses to 129 proteins, with a notable enrichment in autoantibodies targeting antiviral immune response-related proteins and oligodendrocyte marker SOX-10. Machine learning analysis identified a distinct molecular signature comprising 17 differentially expressed autoantibodies, including those against MX1, ISG20, MAX, SUFU, NR1H2, HMGN5, and EPHA10. Among these, autoantibodies against MX1-a key effector in the interferon-alpha/beta signalling pathway-showed the most pronounced increase, with nearly a threefold elevation in MS patients. While MX1 has previously been implicated in MS, this is the first report of autoantibody reactivity against the protein, suggesting a potential role in disease onset and progression. These findings support a link between antiviral immune responses and MS pathophysiology and offer a promising blood-based autoantibody signature that could inform future diagnostic and therapeutic strategies.
KW - Autoantibodies
KW - Biomarkers
KW - ISG20
KW - MX1
KW - Multiple sclerosis
KW - Oligodendrocyte
KW - SOX-10
KW - Viral infection
UR - https://www.scopus.com/pages/publications/105019810498
U2 - 10.1016/j.nbd.2025.107116
DO - 10.1016/j.nbd.2025.107116
M3 - Article
C2 - 41038542
AN - SCOPUS:105019810498
SN - 0969-9961
VL - 216
JO - Neurobiology of Disease
JF - Neurobiology of Disease
M1 - 107116
ER -