Meningeal B Cell Clusters Correlate with Submeningeal Pathology in a Natural Model of Multiple Sclerosis

Molly E Church1, Guadalupe Ceja1, Megan McGeehan1

  • 1Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA.

Insights

Granulomatous meningoencephalomyelitis (GME) in dogs offers a natural model for studying multiple sclerosis (MS). This canine disease shows meningeal inflammation and B cell accumulation, mirroring MS pathology and aiding research into progressive neuroinflammation.

Area of Science:

  • Neuroimmunology
  • Comparative Pathology
  • Neuroinflammation

Background:

  • Multiple sclerosis (MS) is a demyelinating disease where meningeal inflammation accelerates progression.
  • Studying MS meningeal inflammation is challenging due to limited specimen access and lack of progressive MS models.
  • A naturally occurring model is needed for translational research in MS immunopathogenesis.

Purpose of the Study:

  • To propose granulomatous meningoencephalomyelitis (GME) in dogs as a natural model for studying MS neuropathology.
  • To investigate the role of meningeal inflammation and B cell aggregates in GME.
  • To explore the correlation between meningeal pathology and cortical demyelination in GME.

Main Methods:

  • Analysis of GME cases in young dogs, including magnetic resonance imaging (MRI) and histopathological examination.
  • Characterization of leptomeningeal infiltrates, including B cell clusters, tertiary lymphoid organ features, and chemokine expression (CXCL13, CCL21).
  • Comparison of meningeal B cell infiltrates with neuroparenchymal perivascular infiltrates.

Main Results:

  • GME cases showed focal/disseminated leptomeningeal enhancement on MRI, correlating with lymphocytic infiltration.
  • Leptomeningeal infiltrates formed tertiary lymphoid organs with B cell clusters, plasma cells, and follicular dendritic cells.
  • Meningeal B cell accumulation significantly correlated with cortical demyelination, similar to MS.

Conclusions:

  • GME serves as a novel, naturally occurring model for studying compartmentalized neuroinflammation.
  • The meningeal microenvironment in GME sustains B cell accumulation, leading to neuroparenchymal injury.
  • This model provides a framework for understanding the pathology contributing to progressive MS.

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