Gut microbiome-immune interactions and their role in rheumatoid arthritis development

• Published in: PeerJ (San Francisco, CA) Vol. 12; p. e17477
• Main Authors: Nurgaziyev, Madiyar, Issilbayeva, Argul, Bersimbaev, Rakhmetkazhi, Ilderbayev, Oralbek, Vinogradova, Elizaveta, Jarmukhanov, Zharkyn, Nurgozhina, Ayaulym, Sergazy, Shynggys, Kozhabergen, Nuray, Akhmetova, Zhanar, Meiramova, Assel, Chulenbayeva, Laura, Ibrayeva, Aigerim, Mukhanbetzhanov, Nurislam, Mukhanbetzhanova, Zhanel, Kozhakhmetov, Samat, Ainabekova, Bayan, Kushugulova, Almagul
• Format: Journal Article
• Language: English
• Published: United States PeerJ. Ltd 11.07.2024; PeerJ Inc
• Subjects: 16S rRNA; Adult; Analysis; Arthritis; Arthritis, Rheumatoid - immunology; Arthritis, Rheumatoid - microbiology; Biological diversity; Biomarkers - blood; Case-Control Studies; Cytokines; Cytokines - blood; Cytokines - genetics; Cytokines - immunology; Cytokines - metabolism; Ethylenediaminetetraacetic acid; Feces - microbiology; Female; Gastroenterology and Hepatology; Gastrointestinal Microbiome - immunology; Gut microbiome; Humans; Immunology; Kazakhstan; Microbiology; Microbiota (Symbiotic organisms); Middle Aged; Molecular Biology; Rheumatoid arthritis; Rheumatoid factor; Rheumatology; RNA; RNA, Ribosomal, 16S - genetics; Sequencing; Kazakhstan; China; 16S rRNA; Immunology; Cytokines; Rheumatoid arthritis; Metabolic pathways; Gut microbiome; Sequencing; Chemokines
• ISSN: 2167-8359; 2167-8359
• DOI: 10.7717/peerj.17477

The primary objective is to study the impact of gut microbiota and their interactions with diverse immunological markers on the development of rheumatoid arthritis. This study was performed in Astana, Kazakhstan, and included 77 Kazakh female patients older than 18 years, who met the American College of Rheumatology 2010 classification criteria for rheumatoid arthritis (RA), and 113 healthy controls. The DNA was extracted from fecal samples obtained from all study participants for subsequent sequencing at the 16S rRNA gene V1-V3 locus, facilitating the analysis of the gut microbiome. The Multiplex immunoassay was employed to measure the concentrations of inflammatory cytokines, chemokines, and immunoglobulins in both fecal and plasma samples. Our taxonomic analysis revealed significant differences in the composition of the gut microbiota between the healthy control cohort and the cohort with rheumatoid arthritis RA. Alpha diversity was significantly lower in the RA group. were the most abundant taxon and found to be crucial, showing correlations with immunological markers such as IL5. Additionally, and exhibited the most predictable power and distinguished the composition of both study groups. Our study identifies key differences in the gut microbiome of RA patients, revealing distinct microbial patterns and specific taxa abundance. We highlight potential biomarkers in immunological and bacterial pathways, offering insights into RA development and indicating possibilities for personalized treatment.