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Updated: Jan 8, 2026

Generation of Human Chimeric Antigen Receptor Regulatory T Cells
Published on: January 3, 2025
Characterization of the 17 strains of regulatory T cell-inducing human-derived Clostridia
Seiko Narushima1, Yuki Sugiura2, Kenshiro Oshima3
1RIKEN Center for Integrative Medical Sciences (IMS-RCAI); Yokohama, Japan.
Abstract:
The gut microbiota plays important roles in the development of the host immune system. We have previously shown that a combination of 46 strains of commensal Clostridia isolated from conventionally reared mice can induce the accumulation of CD4(+)Foxp3(+) regulatory T (Treg) cells in the mouse colonic lamina propria. Subsequently, we succeeded in isolating and selecting 17 strains of Clostridia from a healthy human fecal sample that can significantly increase the number and function of colonic Treg cells in colonized rodents, thereby attenuating symptoms of experimental allergic diarrhea and colitis. Here we characterize each of the 17 strains of human-derived Clostridia in terms of sensitivity to antibiotics and ability to produce short chain fatty acids and other metabolites, and discuss their potential as biotherapeutics to correct dysbiosis and treat immune-inflammatory diseases.
Insights
Human Clostridia strains boost regulatory T cells in the gut, potentially treating immune disorders. These findings offer new therapeutic avenues for inflammatory conditions.
Area of Science:
- Microbiology
- Immunology
- Gastroenterology
Background:
- The gut microbiota is crucial for immune system development.
- Commensal Clostridia strains can induce regulatory T (Treg) cells in mice.
- Previous work demonstrated Treg cell induction by mouse-derived Clostridia.
Purpose of the Study:
- To characterize 17 human-derived Clostridia strains.
- To assess their potential for Treg cell induction and metabolite production.
- To evaluate their therapeutic potential for immune-inflammatory diseases.
Main Methods:
- Isolation and selection of 17 human Clostridia strains from fecal samples.
- Colonization of rodents to assess Treg cell induction and functional changes.
- Characterization of antibiotic sensitivity and metabolite production (e.g., short-chain fatty acids).
Main Results:
- Human Clostridia strains significantly increased colonic Treg cells in rodents.
- These strains attenuated symptoms of experimental allergic diarrhea and colitis.
- Individual strain characteristics regarding antibiotic sensitivity and metabolite profiles were determined.
Conclusions:
- Human-derived Clostridia strains show promise as biotherapeutics.
- These strains can modulate the host immune system by increasing Treg cells.
- They offer a potential strategy for correcting gut dysbiosis and treating immune-inflammatory diseases.
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