Abstract

The commensal microbiota is in constant interaction with the immune system, teaching immune cells to respond to antigens. Studies in mice have demonstrated that manipulation of the intestinal microbiota alters host immune cell homeostasis. Additionally, metagenomic-sequencing analysis has revealed alterations in intestinal microbiota in patients suffering from inflammatory bowel disease, asthma, and obesity. Perturbations in the microbiota composition result in a deficient immune response and impaired tolerance to commensal microorganisms. Due to altered microbiota composition which is associated to some inflammatory diseases, several strategies, such as the administration of probiotics, diet, and antibiotic usage, have been utilized to prevent or ameliorate chronic inflammatory diseases. The purpose of this review is to present and discuss recent evidence showing that the gut microbiota controls immune system function and onset, development, and resolution of some common inflammatory diseases.

Highlights

  • Commensal microbiota consists of many microorganisms that cover all host mucosal surfaces, but most reside in the gastrointestinal tract, which is the subject of this review

  • GPR41 and GPR43 activation of ERK1/2 is dependent on Gi/o, because the inhibition of this G protein by the pertussis toxin abolishes the stimulatory effect of short chain fatty acids (SCFAs) on this pathway in cells expressing only the GPR41 and reduces it in more than 50% in cells expressing GPR43 alone [27]

  • Microbial signaling is required for immune development and homeostasis, whereas an intact immune system is necessary for maintenance of a healthy gut microbiota

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Summary

Introduction

Commensal microbiota consists of many microorganisms that cover all host mucosal surfaces, but most reside in the gastrointestinal tract, which is the subject of this review. The human body is composed of approximately 100 trillion cells, only 10 trillion are human cells while 90 trillion are microbes The genes of these microorganisms form our metagenome, known as our second genome [1]. The relationship between the gut microbiota and its host plays a key role in immune system maturation, food digestion, drug metabolism, detoxification, vitamin production, and prevention of pathogenic bacteria adhesion [4]. Controlling the intestine’s metabolic products is important for the maintenance of a mutually beneficial relationship between the microbiota and the immune system. When this connection is broken and fails to resolve itself, an inflammatory response is initiated. We review the mechanisms by which the gut microbiota contributes to the development of asthma, bowel disease, and obesity, highlighting the regulatory role of the gut microbiota in immune system function

Mechanisms Linking the Microbiota and Its Products to the Immune System
Asthma
Inflammatory Bowel Disease
Obesity
Findings
Conclusions
Full Text
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