Early identification of individuals at risk for multiple sclerosis by quantification of EBNA-1<sub>381-452</sub>-specific antibody titers.
prospective_cohort · Level II
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- Record sourced from PubMed, PMID 40659624.
- Also identified by DOI 10.1038/s41467-025-61751-9 and PMC identifier 12259891.
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Abstract
Multiple sclerosis (MS) is an immune-mediated demyelinating disease. Epstein-Barr virus (EBV) encodes for the EBNA-1<sub>381-452</sub> region that induces autoreactive antibody responses, which are likely critically involved in MS pathogenesis. Here we investigate whether these EBNA-1<sub>381-452</sub>-specific antibodies can serve as a biomarker to identify at-risk individuals for MS. We quantify EBNA-1<sub>381-452</sub>-specific antibody titers from 324 relapsing-remitting MS patients and 324 matched controls in longitudinal follow-up plasma samples, starting from the individual's EBV-seroconversion. In MS patients, significantly elevated EBNA-1<sub>381-452</sub>-specific IgG titers are identified that are increased already as early as nine months after EBV-seroconversion (OR:5.7; 95% CI: 4.1-8.1; P < 0.0001) and a median 5.4 years prior to MS diagnosis. Especially, the presence of continuously high EBNA-1<sub>381-452</sub>-specific antibody titers is associated with a more rapid MS diagnosis after EBV-seroconversion (P < 0.0001). Thus, the quantification of EBNA-1<sub>381-452</sub>-specific IgG antibody levels may provide a prognostic biomarker to determine the individual's risk for the diagnosis of MS.
Medical subject headings
- Epstein-Barr Virus Nuclear Antigens
- Antibodies, Viral
- Herpesvirus 4, Human
- Multiple Sclerosis
- Epstein-Barr Virus Infections
- Multiple Sclerosis, Relapsing-Remitting