Introduction: The gut microbiota is a complicated and dynamic community of
microorganisms exerting critical regulatory functions in immune homeostasis,
nutrient metabolism, and defense against pathogens. Growing evidence
demonstrates that disruption of microbial balance — referred to as dysbiosis —
recreates a pivotal role in the pathogenesis of a wide range of inflammatory
diseases, including inflammatory bowel disorder (IBD), rheumatoid arthritis,
systemic lupus erythematosus, neurodegenerative conditions, and allergic
disorders. Methods: The present narrative review was conducted using electronic
databases and searches were performed between January 2018 – April 2026. Some
of the important words were: microbes; community of microbes; imbalance of
microbes; swelling; long-chain fatty acids; moving microbes from one place to
another; and ways to treat illness. The study included peer-reviewed articles
published in indexed journals, in English and other languages with available
summaries. Results: Research consistently shows that disease-associated dysbiosis is
characterized by reduced microbial diversity and altered ratios of certain bacteria,
and decreased production of SCFAs. Specific bacteria, for example Faecalibacterium
prausnitzii and Akkermansia muciniphila, have been identified as protective
microorganisms, and their depletion has been linked to increased inflammatory
activity. Therapeutic strategies, including probiotics, prebiotics, dietary
interventions and faecal microbiota transplantation (FMT), offer promising but
variable results across disease states. Conclusion: The gut microbiota constitutes a
modifiable therapeutic target for multiple inflammatory conditions. The future of
precision medicine, multi-omics profiling and personalized nutrition holds great
prospects for microbiota-targeted interventions.
Keywords: gut microbiota; dysbiosis; inflammatory bowel disease; immune
modulation; therapeutic targets
