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Potent inhibition of human enterovirus 71 replication by type I interferon subtypes
Lina Yi1, Yaqing He, Ying Chen
1Stanley Ho Center for Emerging Infectious Diseases, School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong SAR, China.
Background:
Enterovirus 71 (EV71) infection can induce a series of syndromes including herpangina, viraemia, hand-foot-and-mouth disease and even death. Outbreaks of EV71 infection have been reported periodically over the world and have caused a great number of casualties and a high medical expenditure. Some interferons (IFNs) have been used for the treatment of viral infections for decades; however, conventional IFNs only display mild anti-EV71 activities. No effective drug is currently available for the treatment of EV71 infection. Here, we aimed to investigate whether some IFN subtypes display potent anti-EV71 activities.
Methods:
The antiviral activities of 17 type I IFNs were assayed in Vero cells using the cytopathic effect method. Cells were incubated with different concentrations of type I IFNs before or after virus infection. Viral replication was determined by quantitative real-time PCR (qRT-PCR). The expression levels of IFN downstream antiviral genes were also measured by qRT-PCR.
Results:
Out of 17 type I IFNs, 4 IFNs (IFN-α4, IFN-α6, IFN-α14 and IFN-α16) displayed potent antiviral activity. Compared with conventional IFN-α2a, IFN-α14 displayed approximately 20× higher antiviral activity. The superior antiviral effect of IFN-α14 was caused by a strong induction of the downstream antiviral effectors.
Conclusions:
IFN-α14 and three other IFNs could be considered for the treatment of EV71 infection.
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