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Published on: December 16, 2021
Bifidobacterium infantis 35624 modulates host inflammatory processes beyond the gut
David Groeger1, Liam O'Mahony, Eileen F Murphy
1Alimentary Health Ltd., Cork, Ireland.
Bifidobacteria infantis 35624 reduced inflammatory biomarkers in patients with ulcerative colitis, chronic fatigue syndrome, and psoriasis. This probiotic also modulated immune responses in healthy individuals, showing systemic immunomodulatory effects beyond the gut.
Area of Science:
- Immunology
- Microbiology
- Gastroenterology
Background:
- Therapeutic microbes like Bifidobacteria infantis (B. infantis) 35624 can modulate immune responses.
- The systemic effects of B. infantis 35624 on non-gastrointestinal inflammatory conditions are not well understood.
Purpose of the Study:
- To assess the impact of oral B. infantis 35624 on inflammatory biomarkers and cytokines in patients with ulcerative colitis, chronic fatigue syndrome, and psoriasis.
- To evaluate the effect of B. infantis 35624 on immunological biomarkers in healthy subjects.
Main Methods:
- Three randomized, double-blind, placebo-controlled trials involving patients with ulcerative colitis, chronic fatigue syndrome, and psoriasis.
- Assessment of plasma C-reactive protein (CRP), tumor necrosis factor α (TNF-α), and interleukin-6 (IL-6) levels.
- Evaluation of lipopolysaccharide (LPS)-stimulated cytokine secretion by peripheral blood mononuclear cells (PBMCs) in healthy subjects.
Main Results:
- B. infantis 35624 reduced plasma CRP levels in all three inflammatory conditions.
- Plasma TNF-α was reduced in chronic fatigue syndrome and psoriasis patients.
- IL-6 was reduced in ulcerative colitis and chronic fatigue syndrome patients.
- In healthy subjects, B. infantis 35624 reduced LPS-stimulated TNF-α and IL-6 secretion by PBMCs.
Conclusions:
- B. infantis 35624 demonstrates systemic immunomodulatory effects, reducing pro-inflammatory biomarkers in both gastrointestinal and non-gastrointestinal inflammatory conditions.
- The immunomodulatory capacity of the microbiota extends beyond the mucosal immune system to the systemic immune system.
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