Ítem
Solo Metadatos
Human myeloid dendritic cells treated with supernatants of rotavirus infected Caco-2 cells induce a poor Th1 response
Título de la revista
Autores
Rodríguez, Luz-Stella
Narváez, Carlos F.
Rojas, Olga L.
Franco, Manuel A.
Ángel, Juana
Resumen
Abstract
We have previously shown that human myeloid dendritic cells treated with purified rotavirus induce an allogenic Th1 response. To determine if rotavirus in the context of an intestinal microenvironment modulates the function of dendritic cells, we treated these cells with supernatants from non-infected or infected Caco-2 cells and studied their capacity to promote Th1 or Th2 responses. Dendritic cells treated with supernatants from rotavirus-infected Caco-2 cells promoted a significantly lower Th1 response, in comparison with those treated with purified rotavirus. We wanted to establish if TGF-?1, induced, or TSLP, not induced, during rotavirus infection, could mediate this effect. Neutralization of TGF-? but not TSLP in the supernatant prior to treatment of dendritic cells increased their capacity to promote a Th1 response. The results suggest that the TGF-?1 induced by rotavirus could be an immune evasion mechanism, and may partially explain the poor rotavirus-specific T cell response we have previously evidenced. © 2011 Elsevier Inc.
Palabras clave
Keywords
Thymic stromal lymphopoietin , cd86 , Article , Cell strain caco 2 , Cellular immunity , Controlled study , Cytokine production , Human , Human cell , Immunomodulation , Intestine mucosa , Myeloid dendritic cell , Priority journal , Rotavirus infection , Supernatant , Th1 cell , Th2 cell , Virus neutralization , Antigens , Caco-2 cells , Cd4-positive t-lymphocytes , Cellular microenvironment , Coculture techniques , Cytokines , Dendritic cells , Hla-dr antigens , Humans , Immunologic factors , Myeloid cells , Rna , Rotavirus , Rotavirus infections , Th1 cells , Th2 cells , Transforming growth factor beta1 , Tumor cells , Rotavirus , Caco-2 cells , Dendritic cells , Immunomodulators , Rotavirus , Tgf-?1
