4.7 Article

Antibody Content against Epstein-Barr Virus in Blood Extracellular Vesicles Correlates with Disease Activity and Brain Volume in Patients with Relapsing-Remitting Multiple Sclerosis

Journal

Publisher

MDPI
DOI: 10.3390/ijms241814192

Keywords

antibodies; biomarker; Epstein-Barr virus; extracellular vesicles; multiple sclerosis

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This study aimed to investigate the presence of antibodies against EBV antigens in EVs and their potential as diagnostic and disease activity blood biomarkers in RRMS. The results showed that patients with RRMS had higher levels of anti-VCA antibodies in EVs and plasma compared to healthy controls. Patients with active disease also had higher levels of anti-EBNA1 antibodies in EVs. Furthermore, the levels of EV anti-VCA correlated with disease duration and decreased brain volume structures in RRMS.
We aimed to analyze whether EVs carry antibodies against EBV antigens and the possibility that they could serve as diagnostic and disease activity blood biomarkers in RRMS. This was a prospective and observational study including patients with RRMS with active and inactive disease and healthy controls. Blood EVs were isolated by precipitation. Titers of antibodies against nuclear (anti-EBNA1) and capsid (anti-VCA) EBV antigens in EVs and in plasma, as well as content of myelin antibodies in EVs were determined by ELISA. An exploratory analysis of correlations with clinical and radiological data was performed. Patients with RRMS had higher titers of anti-VCA inside EVs and free in plasma than healthy controls. Patients with active disease showed higher levels of anti-EBNA1 in EVs, but not in plasma, than patients with inactive disease. EV anti-VCA levels correlated with disease duration and with decreased brain volume structures-total brain, white matter, gray matter, cerebellum, hippocampus, -but not with T2/FLAIR lesion volume or EDSS, SDMT, or 9HPT. In addition, EV anti-VCA correlated with EV anti-MBP. The anti-VCA and anti-EBNA1 content in EVs could represent diagnostic and disease activity blood biomarkers, respectively, in RRMS.

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