Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/7099
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Título : Bifidobacterium microbiota and parameters of immune function in elderly subjects
Autor : Ouwehand, Arthur C., Bergsma, Nynke, Parhiala, Riikka, Lahtinen, Sampo, Gueimonde Fernández, Miguel, Finne-Soveri, Harriet, Strandberg, Timo, Pitkälä, Kaisu, Salminen, Seppo
Palabras clave : Bifidobacterias
Microbiótica
Ancianos
Citoquinas
Fecha de publicación : 11-Mar-2008
Editor: Federation of European Microbiological Societies
Resumen: Faecal and serum samples were collected over a period of 6 months from 55 institutionalized elderly subjects, who were enrolled in a double-blind placebo-controlled study. Participants were randomized in one of the three treatment groups: intervention (two probiotic Bifidobacterium longum strains: 2C and 46), placebo and commercial control (Bifidobacterium lactis Bb-12). The faecal Bifidobacterium microbiota was characterized by genus and species-specific PCR. Serum levels of the cytokines IL-10, tumor necrosis factor (TNF)-α and transforming growth factor (TGF)-β1 were determined by enzyme-linked immunosorbent assay. Each participant harboured on average approximately three different bifidobacterial species. The most frequently detected species were B. longum, Bifidobacterium adolescentis and Bifidobacterium bifidum. Depending on the treatment, the intervention resulted in specific changes in the levels of certain Bifidobacterium species, and positive correlations were found between the different species. Negative correlations were observed between the levels of Bifidobacterium species and the pro-inflammatory cytokine TNF-α and the regulatory cytokine IL-10. The presence of faecal B. longum and Bifidobacterium animalis correlated with reduced serum IL-10. The anti-inflammatory TGF-β1 levels were increased over time in all three groups, and the presence of Bifidobacterium breve correlated with higher serum TGF-β1 levels. This indicates that modulation of the faecal Bifidobacterium microbiota may provide a means of influencing inflammatory responses
URI : http://hdl.handle.net/10261/7099
DOI: 10.1111/j.1574-695X.2008.00392.x
Citación : FEMS Immunology & Medical Microbiology 53(1): 18-25 (2008)
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