TY - JOUR
T1 - Rupintrivir is a promising candidate for treating severe cases of enterovirus-71 infection
T2 - evaluation of antiviral efficacy in a murine infection model
AU - Zhang, Xiaonan
AU - Song, Zhigang
AU - Qin, Boyin
AU - Zhang, Xiaoling
AU - Chen, Lixiang
AU - Hu, Yunwen
AU - Yuan, Zhenghong
N1 - Crown Copyright © 2013. Published by Elsevier B.V. All rights reserved.
PY - 2013/3
Y1 - 2013/3
N2 - Enterovirus-71 (EV71) infections can cause life-threatening diseases with neurological symptoms. Currently, no direct targeting antivirals are available to combat severe EV71 infection. Rupintrivir (AG7088) is a compound originally designed for Rhinovirus 3C protease. Previous computational analyses by us and crystallography studies by others suggested that rupintrivir is also a high affinity inhibitor to EV71 3C. Thus, we aimed to further evaluate its anti-EV71 activity in vivo at clinically acceptable doses. It was observed that administration of rupintrivir in suckling mice largely protected them from limb paralysis and dramatically improved survival (38.5% DMSO vs. 90.9% at 0.1mg/kg, p=0.006). Histological, immunohistochemical and quantitative RT-PCR analyses confirmed that rupintrivir profoundly alleviated virus induced necrotizing myositis, suppressed viral RNA and blocked EV71 VP1 expression in various tissues. In conclusion, we established that rupintrivir can strongly contain the spread of EV71 infection in vivo at a clinically acceptable dose (as low as 0.1mg/kg). As its safety has been fully tested in previous clinical trials, rupintrivir is suitable for immediate evaluation of potential benefits in EV71-infected individuals with life-threatening neurological symptoms.
AB - Enterovirus-71 (EV71) infections can cause life-threatening diseases with neurological symptoms. Currently, no direct targeting antivirals are available to combat severe EV71 infection. Rupintrivir (AG7088) is a compound originally designed for Rhinovirus 3C protease. Previous computational analyses by us and crystallography studies by others suggested that rupintrivir is also a high affinity inhibitor to EV71 3C. Thus, we aimed to further evaluate its anti-EV71 activity in vivo at clinically acceptable doses. It was observed that administration of rupintrivir in suckling mice largely protected them from limb paralysis and dramatically improved survival (38.5% DMSO vs. 90.9% at 0.1mg/kg, p=0.006). Histological, immunohistochemical and quantitative RT-PCR analyses confirmed that rupintrivir profoundly alleviated virus induced necrotizing myositis, suppressed viral RNA and blocked EV71 VP1 expression in various tissues. In conclusion, we established that rupintrivir can strongly contain the spread of EV71 infection in vivo at a clinically acceptable dose (as low as 0.1mg/kg). As its safety has been fully tested in previous clinical trials, rupintrivir is suitable for immediate evaluation of potential benefits in EV71-infected individuals with life-threatening neurological symptoms.
KW - Animals
KW - Antiviral Agents/administration & dosage
KW - Drug Evaluation, Preclinical
KW - Enterovirus A, Human/drug effects
KW - Enterovirus Infections/drug therapy
KW - Female
KW - Humans
KW - Infant
KW - Isoxazoles/administration & dosage
KW - Male
KW - Mice
KW - Phenylalanine/analogs & derivatives
KW - Pyrrolidinones/administration & dosage
KW - Valine/analogs & derivatives
KW - Virus Replication/drug effects
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-84873030483&origin=resultslist
U2 - 10.1016/j.antiviral.2012.12.029
DO - 10.1016/j.antiviral.2012.12.029
M3 - Article
C2 - 23295352
SN - 0166-3542
VL - 97
SP - 264
EP - 269
JO - Antiviral Research
JF - Antiviral Research
IS - 3
ER -