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Mucosal Immunol ; 10(6): 1569-1580, 2017 11.
Artículo en Inglés | MEDLINE | ID: mdl-28295020

RESUMEN

Regulation of respiratory mucosal immunity by microbial-derived metabolites has been a proposed mechanism that may provide airway protection. Here we examine the effect of oral Lactobacillus johnsonii supplementation on metabolic and immune response dynamics during respiratory syncytial virus (RSV) infection. L. johnsonii supplementation reduced airway T helper type 2 cytokines and dendritic cell (DC) function, increased regulatory T cells, and was associated with a reprogrammed circulating metabolic environment, including docosahexanoic acid (DHA) enrichment. RSV-infected bone marrow-derived DCs (BMDCs) from L. johnsonii-supplemented mice had altered cytokine secretion, reduced expression of co-stimulatory molecules, and modified CD4+ T-cell cytokines. This was replicated upon co-incubation of wild-type BMDCs with either plasma from L. johnsonii-supplemented mice or DHA. Finally, airway transfer of BMDCs from L. johnsonii-supplemented mice or with wild-type derived BMDCs pretreated with plasma from L. johnsonii-supplemented mice reduced airway pathological responses to infection in recipient animals. Thus L. johnsonii supplementation mediates airway mucosal protection via immunomodulatory metabolites and altered immune function.


Asunto(s)
Células de la Médula Ósea/inmunología , Células Dendríticas/inmunología , Lactobacillus johnsonii/inmunología , Infecciones por Virus Sincitial Respiratorio/inmunología , Virus Sincitiales Respiratorios/inmunología , Linfocitos T Reguladores/metabolismo , Células Th2/metabolismo , Animales , Células de la Médula Ósea/virología , Línea Celular , Microambiente Celular , Reprogramación Celular , Citocinas/metabolismo , Células Dendríticas/virología , Suplementos Dietéticos , Ácidos Docosahexaenoicos/metabolismo , Inmunomodulación , Activación de Linfocitos , Ratones , Ratones Endogámicos BALB C , Infecciones por Virus Sincitial Respiratorio/prevención & control , Linfocitos T Reguladores/inmunología , Células Th2/inmunología
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