Abstract

Neuroinflammation can be defined as an inflammatory response within the central nervous system (CNS) mediated by a complex crosstalk between CNS-resident and infiltrating immune cells from the periphery. Triggers for neuroinflammation not only include pathogens, trauma and toxic metabolites, but also autoimmune diseases such as neuromyelitis optica spectrum disorders and multiple sclerosis (MS) where the inflammatory response is recognized as a disease-escalating factor. B cells are not considered as the first responders of neuroinflammation, yet they have recently gained focus as a key component involved in the disease pathogenesis of several neuroinflammatory disorders like MS. Traditionally, the prime focus of the role of B cells in any disease, including neuroinflammatory diseases, was their ability to produce antibodies. While that may indeed be an important contribution of B cells in mediating disease pathogenesis, several lines of recent evidence indicate that B cells are multifunctional players during an inflammatory response, including their ability to present antigens and produce an array of cytokines. Moreover, interaction between B cells and other cellular components of the immune system or nervous system can either promote or dampen neuroinflammation depending on the disease. Given that the interest in B cells in neuroinflammation is relatively new, the precise roles that they play in the pathophysiology and progression of different neuroinflammatory disorders have not yet been well-elucidated. Furthermore, the possibility that they might change their function during the course of neuroinflammation adds another level of complexity and the puzzle remains incomplete. Indeed, advancing our knowledge on the role of B cells in neuroinflammation would also allow us to tackle these disorders better. Here, we review the available literature to explore the relationship between autoimmune and infectious neuroinflammation with a focus on the involvement of B cells in MS and viral infections of the CNS.

Highlights

  • The primary focus of B cells as enhancers of autoimmunity was their exclusive ability to differentiate into plasma cells and produce autoantibodies

  • We focus on multiple sclerosis (MS), which is a classical example of autoimmune neuroinflammation and on the other hand we extend our discussion by drawing parallels between MS and virus-induced neuroinflammation with respect to the involvement of B cells

  • One can say that the B cell response in neuroinflammation is complex and comprises a combination of both beneficial and detrimental phenotypes

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Summary

INTRODUCTION

The primary focus of B cells as enhancers of autoimmunity was their exclusive ability to differentiate into plasma cells and produce autoantibodies. A large volume of literature emphasizes on the heterogenous roles of B cells in autoimmunity and peripheral inflammation, yet our understanding of the extent of B cell involvement in autoimmune neuroinflammation remains incomplete. We discuss the literature available on how B cells are involved in two different instances of neuroinflammation by highlighting their beneficial and detrimental roles in ameliorating or aggravating disease pathophysiology, respectively. We focus on MS, which is a classical example of autoimmune neuroinflammation and on the other hand we extend our discussion by drawing parallels between MS and virus-induced neuroinflammation with respect to the involvement of B cells

GENERAL INTRODUCTION TO B CELL BIOLOGY
An Overview of the Disease
Evidence of B Cells in MS
Role of B Cells in MS
Viral Infections of the CNS
Viral Infections Related to MS
CONCLUDING REMARKS
Findings
AUTHOR CONTRIBUTIONS
Full Text
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