In this study, the contribution of
type I interferons (IFNs) to protection against
infection with enterovirus 71 (EV71) was investigated using a murine model where the virus was administrated to neonatal Institute of
Cancer Research (ICR) mice by either the intraperitoneal (i.p.) or the oral route. In i.p. inoculated mice, post-
infection treatment of
dexamethasone (5 mg kg(-1) at 2 or 3 days after
infection) exacerbated clinical symptoms and increased the tissue viral titre. In contrast,
polyriboinosinic : polyribocytidylic acid [
poly(I : C); 10 or 100 microg per mouse at 12 h before
infection], a potent IFN inducer, improved the survival rate and decreased the tissue viral titres after EV71 challenge, which correlated with an increase in serum IFN-alpha concentration, the percentage of dendritic cells, their expression of major histocompatibility complex class II molecule and IFN-alpha in spleen. Treatment with a
neutralizing antibody for type I IFNs (10(4) neutralizing units per mouse, 6 h before and 12 h after
infection) resulted in frequent deaths and higher tissue viral load in infected mice compared with control mice. In contrast, an early administration of recombinant mouse IFN-alphaA (10(4) U per mouse for 3 days starting at 0, 1 or 3 days after
infection) protected the mice against EV71
infection. In vitro analysis of virus-induced death in three human cell lines showed that human type I IFNs exerted a direct protective effect on EV71. It was concluded that type I IFNs play an important role in controlling EV71
infection and replication.