Abstract

Recently, there has been a substantial increase in the number of studies focused upon connecting the gut microbiome with cases of central nervous system (CNS) autoimmunity. Multiple sclerosis (MS) is a neurodegenerative autoimmune disorder of the CNS. Recent experimental and clinical evidence suggests the presence of microbial imbalances in the gut of MS sufferers. The gut microbiome is defined as the summation of all the microbial entities as well as their genes, proteins, and metabolic products in a given space and time. Studies show the MS gut microbiome as having general alterations in specific taxa, some associated with the promotion of inflammatory cytokines and overall inflammation. In conjunction with these findings, experimental models of the disease have reported that T regulatory (Treg) cells have deficits in their function as a result of the aberrant gut microbiota composition. The findings suggest that the interactions between the host and the microbiota are reciprocal, although more extensive work is required to confirm this. Moreover, evidence indicates that changes in microbiota composition may result in imbalances that could result in disease, with the gut as a potential novel therapeutic avenue. By understanding the biological effects of aberrant gut microbiome composition, it is possible to contemplate current therapeutic options and their efficacy. Ultimately, more research is necessary in this field, but targeting the gut microbiota may lead to the development of novel therapeutic strategies.

Highlights

  • We found that the mice which developed a severe secondary form of EAE harbored a dysbiotic gut microbiome when compared to the healthy control mice, and that the differences were observed at early stages of disease [45]

  • The oral delivery of phage has been considered to be safe and have the capability to bypass intestinal epithelia and penetrate the gut-associated lymphoid tissue (GALT) as well as the blood stream [78,79]. This ability to penetrate the GALT as well as the blood stream makes phage therapy extremely attractive to deal with bacterial translocation that can lead to diseased states

  • All the potential new therapeutic options discussed in this review have not been explored fully for Multiple sclerosis (MS)

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Summary

Introduction

Diverse bacterial metabolism allows them to occupy almost every possible niche on Earth. Every facet of human biology is exposed to bacteria. Commensal microbes will reside in or on the human host and receive nutrients from their host’s diet and or metabolites produced from other bacteria. These microbes do not benefit their host, but they are not detrimental either. As science continues to investigate the bacteria associated with humans, their apparent function and benefits become more apparent. The microbiota can potentially affect the onset and progression of diseases defined by several effector cells and soluble metabolic, immune, and neuroendocrine factors modulated by gut microbes. In this review article we discuss the proposed association established between the gut microbiota and MS

The Gut Microbiome
The Anatomy of the Gut Epithelium
Multiple Sclerosis and Autoimmunity
The Gut Microbiome and Multiple Sclerosis
Targeting the Gut Microbiome with Therapeutic Options
Antibiotic Therapy
Phage Therapy
Fecal Microbiota Transplantation
Dietary Supplementation
Probiotics and Immunomodulatory Factors Derived from Gut Microbes
Findings
Concluding Remarks
Full Text
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