Abstract

Neuroinflammation is a prominent pathological feature of all neuroimmunological diseases, including, but not limited to, multiple sclerosis (MS), myasthenia gravis, neuromyelitis optica, and Guillain–Barré syndrome. All currently-approved therapies for the treatment of these diseases focus on controlling or modulating the immune (innate and adaptive) responses to limit demyelination and neuronal damage. The primary purpose of this review is to detail the pre-clinical data and proposed mechanism of action of novel drugs currently in clinical trial, with a focus on novel compounds that promote repair and regeneration in the central nervous system (CNS). As the most recent advances have been made in the field of MS research, this review will focus primarily on this disease and its animal models. However, these compounds are likely to be effective for a range of indications with a neuroinflammatory component. Traditionally, MS was thought to proceed through two distinct phases. The first, predominantly inflammatory stage, is characterized by acute episodes of clinical relapse, followed by periods of partial or total recovery with an apparent absence of overall disease progression. In the vast majority of patients, this relapsing-remitting disease subsequently progresses into a second more chronic, neurodegenerative phase, which is characterized by oligodendrocyte damage and axonal destruction leading to brain atrophy and an accumulation of disability. Recent work has shown that rather than occurring independently, both the inflammatory and degenerative phases may run concurrently. This, combined with evidence that early therapeutic intervention slows accumulation of disability and delays progression, highlights the need for novel therapeutic approaches that promote repair and regeneration early in the disease trajectory. Such compounds may be used as monotherapies or in conjunction with classical anti-inflammatory therapies. This review will highlight novel therapies currently in clinical trial, and likely to appear in clinical practice in the near future, focusing on compounds that target the immune system and/or enhance endogenous repair mechanisms in the CNS.

Highlights

  • Neuroimmunology is the multidisciplinary study of the interaction between the immune, central, and peripheral nervous systems

  • This study aims to measure the change from baseline of best corrected visual acuity at 100% contrast between treatment groups

  • As current patient cohorts spend longer on the newer generation of immunomodulatory compounds, we will begin to understand if preventing inflammatory activity early in relapsing-remitting MS (RRMS) delays and/or prevents progression

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Summary

Introduction

Neuroimmunology is the multidisciplinary study of the interaction between the immune, central, and peripheral nervous systems. In the past decade this moniker has been appropriated to describe changes ( in resident glia) that fall within the confines of a normal glial response. The advent of “omics” level-interrogation of human disease tissue in conjunction with large, highly reproducible genome-wide association studies (GWAS) have positioned immune cells and their products at the center of discussions on the pathological causes and drivers of neurological disease. These include neurodegenerative diseases (Alzheimer’s, Parkinson’s, Huntington’s and amyotrophic lateral sclerosis), neurodevelopmental disorders such as autism spectrum disorders, and mental health illnesses such as schizophrenia [3]

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