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Virology ; 394(2): 235-42, 2009 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-19765789

RESUMEN

Active infection with torquetenovirus (TTV) has been associated with an increased severity of diseases in which inflammation plays a particularly important pathogenetic role. Here, we report that cloned DNA of a genogroup 4 TTV (ViPiSAL) is an activator of proinflammatory cytokine production by murine spleen cells and that the effect is mediated via toll-like receptor (TLR)9. The same DNA also increased the levels of proinflammatory cytokines induced by two well-characterized TLR9 stimulants. Finally, in silico analyses of the genomes of ViPiSAL and other TTVs revealed marked differences in the representation of CpG motifs known to be most effective at activating immune cells via TLR9. These findings demonstrate for the first time that at least one TTV isolate has the potential to stimulate and co-stimulate inflammatory responses.


Asunto(s)
Citocinas/biosíntesis , ADN Viral/inmunología , Mediadores de Inflamación/metabolismo , Receptor Toll-Like 9/metabolismo , Torque teno virus/inmunología , Animales , Células Cultivadas , Islas de CpG , Citocinas/genética , ADN Viral/química , ADN Viral/genética , Expresión Génica , Genoma Viral , Interacciones Huésped-Patógeno/genética , Interacciones Huésped-Patógeno/inmunología , Humanos , Interferón gamma/biosíntesis , Interferón gamma/genética , Interleucina-10/biosíntesis , Interleucina-10/genética , Interleucina-6/biosíntesis , Interleucina-6/genética , Ratones , Bazo/citología , Bazo/inmunología , Bazo/virología , Torque teno virus/clasificación , Torque teno virus/genética , Torque teno virus/patogenicidad
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