Research news
Epstein-Barr Virus (EBV) infection – the infection pathogen behind so-called 'glandular fever' – is a risk factor for multiple sclerosis (MS), but the exact mechanisms involved have been unclear. Now, Joona Sarkkinen and colleagues reveal how EBV-driven changes to B cells in the deep cervical lymph nodes (dcLNs) of patients with MS may contribute to disease progression.
These findings provide valuable insights into MS development in humans, which may be difficult to capture in animal models of disease. MS is characterized by B cell-mediated autoimmunity. Prior research has shown that the dcLNs are the site of anti-EBV adaptive immune responses, and that they are enlarged in patients with MS, compared to healthy individuals.
However, it has been unclear how EBV might drive changes to the dcLN immune landscape. To investigate, Sarkkinen et al. examined dcLN biopsies from 6 newly diagnosed patients with MS and 3 healthy controls. They found reduced numbers of B cells and follicular helper T (TFH) cells in the germinal centre (GC), and an expanded subset of memory B cells in patients with MS.
The memory B cells, along with some GC B cells, had transcriptional signatures that matched those seen in EBV-infected B cells. Using T cell receptor sequencing, the researchers observed an enrichment of EBV-targeting cytotoxic T cells in some patients with MS and noted that the T cells showed altered profiles and signs of immune exhaustion.
Several patients with MS had elevated levels of EBV DNA in the dcLNs, as well as increased EBV and herpes viruses in the saliva, when compared to healthy controls. The authors suggest that the increased viral loads in patients with MS may be due to EBV reactivation.
“These findings suggest that EBV-driven B cell dysregulation is a critical mechanism in MS pathogenesis,” wrote Sarkinnen et al.
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https://doi.org/10.1126/science.abj8222
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