| Literature DB >> 21676485 |
Andrezza F Santiago1, Andréa C Alves, Rafael P Oliveira, Raphaela M Fernandes, Josiely Paula-Silva, Frankcineia A Assis, Cláudia R Carvalho, Howard L Weiner, Ana Maria C Faria.
Abstract
Aging is reported to be associated with decline in oral tolerance induction, which is initiated at the intestinal mucosal surface. Herein, we examined the effect of aging in T cells and cytokines at the intestinal mucosa that might be involved in oral tolerance induction. Frequencies of regulatory-type IEL subsets such as TCRγδ(+) and TCRαβ(+)CD8αα(+) were lower in aged mice. Mucosal CD4(+)CD25(+)Foxp3(+) and CD4(+)LAP(+) T cells increased with aging but activated CD44(+)CD4(+) mucosal T cells also augmented. Production of TGF-β and IL-10 in the small intestine of old mice was reduced. Moreover, the ability of mucosal dendritic cells of aged mice to stimulate TGF-β secretion and differentiation of CD4(+)LAP(+) T cells in co-culture studies also declined with aging. Reduction in these regulatory-type cytokines and T cells may help to explain the decline in susceptibility to oral induction during aging. However, not all mucosal regulatory elements were altered by aging and CD4(+)CD25(+)Foxp3(+) T cells were especially resistant to changes. Persistence of some mechanisms of regulation may play a critical role in maintaining mucosal homeostasis during aging.Entities:
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Year: 2011 PMID: 21676485 PMCID: PMC3206609 DOI: 10.1016/j.imbio.2011.05.007
Source DB: PubMed Journal: Immunobiology ISSN: 0171-2985 Impact factor: 3.144