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1.
Sci Rep ; 6: 30277, 2016 07 25.
Artigo em Inglês | MEDLINE | ID: mdl-27452116

RESUMO

Non-fermenting Gram-negative bacilli, such as Sphingomonas paucimobilis (S.paucimobilis), are among the most widespread causes of nosocomial infections. Up to now, no definitive guidelines exist for antimicrobial therapy for S. paucimobilis infections. As we have shown that some dietary fibers exhibit pronounced immune-regulatory properties, we hypothesized that specific immune active dietary fibers might modulate the responses against S. paucimobilis. We studied the immunomodulatory effects of dietary fibers against S. paucimobilis on cytokine release and maturation of human dendritic cells (DCs) in co-cultures of DCs and intestinal epithelial cells (IECs). S. paucimobilis infection resulted in increased release of pro-inflammatory cytokines and chemokines by DCs/IECs; these effects were strongly attenuated by specific dietary fibers. Chicory inulin, sugar beet pectin, and both starches had the strongest regulatory effects. IL-12 and TNF-α were drastically diminished upon exposure to chicory inulin and sugar beet pectin, or both starches. High-maize 260, was more effective in the reduction of chemokine release than the others fibers tested. In summary, chicory inulin, sugar beet pectin, High-maize 260, and Novelose 330 attenuate S. paucimobilis-induced cytokines. These results demonstrate that dietary fibers with a specific chemical composition can be used to manage immune responses against pathogens such as S. paucimobilis.


Assuntos
Infecção Hospitalar/dietoterapia , Células Dendríticas/efeitos dos fármacos , Fibras na Dieta/farmacologia , Células Epiteliais/efeitos dos fármacos , Técnicas de Cocultura , Infecção Hospitalar/imunologia , Infecção Hospitalar/microbiologia , Células Dendríticas/imunologia , Células Epiteliais/imunologia , Humanos , Imunomodulação/efeitos dos fármacos , Interleucina-12/genética , Inulina/química , Inulina/farmacologia , Pectinas/química , Pectinas/farmacologia , Sphingomonas/efeitos dos fármacos , Sphingomonas/imunologia , Sphingomonas/patogenicidade , Amido/química , Amido/farmacologia , Fator de Necrose Tumoral alfa/genética
2.
Mol Nutr Food Res ; 59(4): 698-710, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25620425

RESUMO

SCOPE: In the present study, the direct interaction of commonly consumed fibers with epithelial or dendritic cells (DCs) was studied. METHODS AND RESULTS: The fibers were characterized for their sugar composition and chain length profile. When in direct contact, fibers activate DCs only mildly. This was different when DCs and fibers were co-cultured together with supernatants from human epithelial cells (Caco spent medium). Caco spent medium enhanced the production of IL-12, IL-1Ra, IL-6, IL-8, TNF-α, MCP-1 (monocyte chemotactic protein), and MIP-1α but this was strongly attenuated by the dietary fibers. This attenuating effect on proinflammatory cytokines was dependent on the interaction of the fibers with Toll-like receptors as it was reduced by Pepinh-myd88. The interaction of galacto-oligosaccharides, chicory inulin, wheat arabinoxylan, barley ß-glucan with epithelial cells and DCs led to changes in the production of the Th1 cytokines in autologous T cells, while chicory inulin, and barley ß-glucan reduced the Th2 cytokine IL-6. The Treg-promoting cytokine IL-10 was induced by galacto-oligosaccharides whereas chicory inulin decreased the IL-10 production. CONCLUSIONS: Our results suggest that dietary fibers can modulate the host immune system not only by the recognized mechanism of effects on microbiota but also by direct interaction with the consumer's mucosa. This modulation is dietary fiber type dependent.


Assuntos
Células Dendríticas/efeitos dos fármacos , Fibras na Dieta/farmacologia , Células Epiteliais/efeitos dos fármacos , Intestinos/citologia , Beta vulgaris/química , Células CACO-2 , Células Cultivadas , Quimiocina CCL2/metabolismo , Quimiocina CCL3/metabolismo , Cichorium intybus/química , Células Epiteliais/metabolismo , Hordeum/química , Humanos , Proteína Antagonista do Receptor de Interleucina 1/metabolismo , Interleucina-10/metabolismo , Interleucina-12/metabolismo , Interleucina-6/metabolismo , Interleucina-8/metabolismo , Mucosa Intestinal/metabolismo , Inulina/farmacologia , Pectinas/farmacologia , Triticum/química , Fator de Necrose Tumoral alfa/metabolismo , Xilanos/farmacologia , beta-Glucanas/farmacologia
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