Lipid-specific IgMs induce antiviral responses in the CNS: implications for progressive multifocal leukoencephalopathy in multiple sclerosis

  • Acta Neuropathol Commun. 2020 Aug 13;8(1):135. doi: 10.1186/s40478-020-01011-7.
Lorna Hayden  1 Tiia Semenoff  1 Verena Schultz  1 Simon F Merz  1 Katie J Chapple  1 Moses Rodriguez  2 Arthur E Warrington  2 Xiaohong Shi  1 Clive S McKimmie  3 Julia M Edgar  1 Katja Thümmler  1 Chris Linington  1 Marieke Pingen  4
Affiliations
  • 1. Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, G12 8TA, UK.
  • 2. Departments of Neurology and Neurosurgery, Mayo Clinic, Rochester, MN, USA.
  • 3. Virus Host Interaction Team, Leeds Institute of Medical Research, School of Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS9 7TF, UK.
  • 4. Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, G12 8TA, UK. [email protected].
Abstract

Progressive multi-focal leukoencephalopathy (PML) is a potentially fatal encephalitis caused by JC polyomavirus (JCV). PML principally affects people with a compromised immune system, such as patients with multiple sclerosis (MS) receiving treatment with natalizumab. However, intrathecal synthesis of lipid-reactive IgM in MS patients is associated with a markedly lower incidence of natalizumab-associated PML compared to those without this antibody repertoire. Here we demonstrate that a subset of lipid-reactive human and murine IgMs induce a functional anti-viral response that inhibits replication of encephalitic Alpha and Orthobunyaviruses in multi-cellular central nervous system cultures. These lipid-specific IgMs trigger microglia to produce IFN-β in a cGAS-STING-dependent manner, which induces an IFN-α/β-receptor 1-dependent Antiviral response in glia and neurons. These data identify lipid-reactive IgM as a mediator of anti-viral activity in the nervous system and provide a rational explanation why intrathecal synthesis of lipid-reactive IgM correlates with a reduced incidence of iatrogenic PML in MS.

Keywords
IgM; Interferon stimulated genes; John Cunningham polyomavirus (JCV); Microglia; Type-I interferon; Viral encephalitis.
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