Therapeutic Potential of a Novel Bifidobacterium Identified Through Microbiome Profiling of RA Patients With Different RF Levels
The potential therapeutic effects of probiotic bacteria in rheumatoid arthritis (RA) remain controversial. Thus, this study aimed to discover potential therapeutic bacteria based on the relationship between the gut microbiome and rheumatoid factor (RF) in RA. Bacterial genomic DNA was extracted from...
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Published in | Frontiers in immunology Vol. 12; p. 736196 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
15.11.2021
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Subjects | |
Online Access | Get full text |
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Summary: | The potential therapeutic effects of probiotic bacteria in rheumatoid arthritis (RA) remain controversial. Thus, this study aimed to discover potential therapeutic bacteria based on the relationship between the gut microbiome and rheumatoid factor (RF) in RA. Bacterial genomic DNA was extracted from the fecal samples of 93 RA patients and 16 healthy subjects. Microbiota profiling was conducted through 16S rRNA sequencing and bioinformatics analyses. The effects of
Bifidobacterium
strains on human peripheral blood mononuclear cells and collagen-induced arthritis (CIA) mice were assessed. Significant differences in gut microbiota composition were observed in patients with different RF levels. The relative abundance of
Bifidobacterium
and
Collinsella
was lower in RF-high than in RF-low and RF-negative RA patients, while the relative abundance of
Clostridium
of Ruminococcaceae family was higher in RF-high than in RF-low and RF-negative patients. Among 10 differentially abundant
Bifidobacterium
,
B. longum
RAPO exhibited the strongest ability to inhibit IL-17 secretion. Oral administration of
B. longum
RAPO in CIA mice, obese CIA, and humanized avatar model significantly reduced RA incidence, arthritis score, inflammation, bone damage, cartilage damage, Th17 cells, and inflammatory cytokine secretion. Additionally,
B. longum
RAPO significantly inhibited Th17 cells and Th17-related genes—
IL-17A
,
IRF4
,
RORC
,
IL-21
, and
IL-23R
—in the PBMCs of rheumatoid arthritis patients. Our findings suggest that
B. longum
RAPO may alleviate RA by inhibiting the production of IL-17 and other proinflammatory mediators. The safety and efficacy of
B. longum
RAPO in patients with RA and other autoimmune disorders merit further investigation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Poornima Paramasivan, Concept Life Sciences, United Kingdom Reviewed by: Magdalena Zoledziewska, Institute of Genetic and Biomedical Research (CNR), Italy; Chia-Yu Yang, Chang Gung University, Taiwan These authors have contributed equally to this work This article was submitted to Autoimmune and Autoinflammatory Disorders, a section of the journal Frontiers in Immunology |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2021.736196 |