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A new serological autoantibody signature associated with multiple sclerosis

  • Houari Abdesselem*
  • , Alberto de la Fuente
  • , Ilham Bensmail
  • , Israa E. Elbashir
  • , Diana Anuar
  • , Tan Ti-Myen
  • , Bermet Abylova
  • , Jonathan M. Blackburn
  • , Rayaz A. Malik
  • , Ioannis N. Petropoulos
  • *Corresponding author for this work
  • Hamad bin Khalifa University
  • Sengenics Corporation
  • University of Cape Town
  • Qatar Foundation HQ

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Article number107116
JournalNeurobiology of Disease
Volume216
DOIs
Publication statusPublished - Nov 2025

Keywords

  • Autoantibodies
  • Biomarkers
  • ISG20
  • MX1
  • Multiple sclerosis
  • Oligodendrocyte
  • SOX-10
  • Viral infection

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