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- W1837114092 abstract "Vasoactive intestinal polypeptide (VIP) is an important signal molecule of the neuroendocrine-immune network. In the immune system, VIP has been found to act as an endogenous anti-inflammatory mediator. In the current study, it was found that VIP administration regulated oral tolerance by inhibiting both cellular and humoral responses. Compared with vehicle-treated mice, mice treated with VIP during the development of ovalbumin (OVA)-induced oral tolerance exhibited the least delayed-type hypersensitivity (DTH), showed profoundly reduced proliferative capacity and produced less interferon (IFN)-gamma, interleukin (IL)-6, IL-5, IL-10 and interferon-inducible protein (IP-10). IgA-secreting cells in the gut as well as OVA-specific IgG and other isotypes levels in plasma were inhibited significantly after VIP-treatment. The VPAC2 receptor may be involved in VIP-mediated oral tolerance enhancement. Taken together, these results suggest that VIP enhanced oral tolerance via regulating both cellular and humoral responses." @default.
- W1837114092 created "2016-06-24" @default.
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- W1837114092 date "2007-01-26" @default.
- W1837114092 modified "2023-09-25" @default.
- W1837114092 title "Vasoactive intestinal polypeptide enhances oral tolerance by regulating both cellular and humoral immune responses" @default.
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- W1837114092 doi "https://doi.org/10.1111/j.1365-2249.2007.03322.x" @default.
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