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.
Abstract:
Multiple sclerosis (MS) is an idiopathic demyelinating disease in which meningeal inflammation correlates with accelerated disease progression. The study of meningeal inflammation in MS has been limited because of constrained access to MS brain/spinal cord specimens and the lack of experimental models recapitulating progressive MS. Unlike induced models, a spontaneously occurring model would offer a unique opportunity to understand MS immunopathogenesis and provide a compelling framework for translational research. We propose granulomatous meningoencephalomyelitis (GME) as a natural model to study neuropathological aspects of MS. GME is an idiopathic, progressive neuroinflammatory disease of young dogs with a female bias. In the GME cases examined in this study, the meninges displayed focal and disseminated leptomeningeal enhancement on magnetic resonance imaging, which correlated with heavy leptomeningeal lymphocytic infiltration. These leptomeningeal infiltrates resembled tertiary lymphoid organs containing large B cell clusters that included few proliferating Ki67+ cells, plasma cells, follicular dendritic/reticular cells, and germinal center B cell-like cells. These B cell collections were confined in a specialized network of collagen fibers associated with the expression of the lympho-organogenic chemokines CXCL13 and CCL21. Although neuroparenchymal perivascular infiltrates contained B cells, they lacked the immune signature of aggregates in the meningeal compartment. Finally, meningeal B cell accumulation correlated significantly with cortical demyelination reflecting neuropathological similarities to MS. Hence, during chronic neuroinflammation, the meningeal microenvironment sustains B cell accumulation that is accompanied by underlying neuroparenchymal injury, indicating GME as a novel, naturally occurring model to study compartmentalized neuroinflammation and the associated pathology thought to contribute to progressive MS.
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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