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Published on: June 24, 2020
The role of intestinal bifidobacteria on immune system development in young rats
Ping Dong1, Yi Yang, Wei-ping Wang
1Children's Hospital, Pediatrics Department of Shanghai Medical College, Fudan University, Shanghai, PR China.
Insights
Intestinal bifidobacteria significantly impact early life immunity. Supplementation promotes immune cell maturation and enhances antibody production, while minimization delays these crucial developmental processes.
Area of Science:
- Immunology
- Microbiology
- Gastroenterology
Background:
- Early life gut microbiota composition is critical for immune system development.
- Intestinal bifidobacteria play a key role in shaping host immunity from birth.
Purpose of the Study:
- To investigate the effects of intestinal bifidobacteria on the development of the immune system in neonatal rats.
- To determine how manipulating bifidobacteria levels influences immune cell maturation and function.
Main Methods:
- Neonatal Sprague Dawley rats were divided into two groups: one with minimized bifidobacteria (antibiotic-treated) and one supplemented with Bifidobacterium longum.
- Immune development indices, including dendritic cell maturation, T cell development, cytokine production, and antibody synthesis, were assessed at 1, 3, and 6 weeks of age.
Main Results:
- Minimizing bifidobacteria delayed dendritic cell and T cell maturation, altered cytokine profiles (increased IL-4, decreased IL-12, IL-10, IFN-γ), and reduced immunoglobulin-M production.
- Bifidobacteria supplementation promoted dendritic cell maturation, enhanced IL-12, IL-10, and interferon-gamma (IFN-γ) mRNA expression, and increased immunoglobulin-M secretion.
Conclusions:
- Intestinal bifidobacteria are essential for promoting dendritic cell maturation and IL-12 expression in the gut.
- Bifidobacteria influence T cell development in the thymus, support T-helper cell type 1 responses via IFN-γ, and regulate T regulatory cell responses through IL-10.
- These bacteria enhance antibody synthesis by peripheral blood mononuclear cells (PBMCs), contributing to both gut and systemic immunity development in early life.
Aim:
The effects of intestinal bifidobacteria on the development of immunity in early life were explored.
Methods:
Neonatal SD rats born and housed under strict barrier systems were fed from birth with sufficient antibiotics (bifidobacteria minimisation group) or supplemented daily with 1x10(10) colony-forming units of live Bifidobacterium longum (bifidobacteria supplementation group). Relevant indices of immune development were determined at one, three and six weeks old.
Results:
Compared to the control group, minimisation of the intestinal bifidobacteria delayed maturation of dendritic cells in Peyer's Patches and the development of T cells in the thymus, increased IL-4 secretion in the plasma, down-regulated IL-12, IL-10 mRNA and the interferon-gamma/IL-4 mRNA ratio in intestinal mucosa, decreased interferon-gamma mRNA in cultured peripheral blood mononuclear cells (PBMCs), and reduced immunoglobulin-M production in cultured PBMCs. Conversely, supplementation with bifidobacteria promoted dendritic cell maturation in Peyer's Patches, up-regulated IL-12, IL-10, interferon-gamma mRNA and the interferon-gamma/IL-4 ratio in intestinal mucosa, increased interferon-gamma gene expression in cultured PBMCs, and raised immunoglobulin-M secretion in cultured PBMCs.
Conclusions:
Intestinal bifidobacteria could promote the maturation of dendritic cells and its expression of IL-12 locally in the gut, influence the development of T cells in the thymus, favour the development of T-helper cell type 1 response by increasing the local and systemic expression of interferon-gamma and ensure the intestinal regulatory T cell response by promoting the local expression of IL-10. In addition, they enhance antibody synthesis by PBMCs, thereby affecting the development of both the gut and systemic immunity in early life.
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