In Vivo Time-Related Evaluation of a Therapeutic Neutralization Monoclonal Antibody against Lethal Enterovirus 71 Infection in a Mouse Model

被引:17
作者
Li, Zhiqun [1 ]
Xu, Longfa [1 ,2 ]
He, Delei [1 ,2 ]
Yang, Lisheng [1 ]
Liu, Che [1 ]
Chen, Yixin [1 ,2 ]
Shih, James Wai Kuo [1 ,2 ]
Zhang, Jun [1 ,2 ]
Zhao, Qinjian [1 ,2 ]
Cheng, Tong [1 ,2 ]
Xia, Ningshao [1 ,2 ]
机构
[1] Xiamen Univ, Sch Life Sci, State Key Lab Mol Vaccinol & Mol Diagnost, Xiamen, Fujian, Peoples R China
[2] Xiamen Univ, Sch Publ Hlth, Natl Inst Diagnost & Vaccine Dev Infect Dis, Xiamen, Fujian, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 10期
基金
中国国家自然科学基金;
关键词
BRAIN-STEM ENCEPHALITIS; MOUTH-DISEASE; VIRUS; MICE; ENCEPHALOMYELITIS; CHALLENGE; EPIDEMIC; OUTBREAK; CHILDREN; HAND;
D O I
10.1371/journal.pone.0109391
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Enterovirus 71 (EV71) is a neurotropic virus capable of inducing severe neurological symptoms and death. No direct targeting antivirals are useful in the treatment of severe EV71 infection. Because of low toxicity and good specificity, monoclonal antibodies (MAb) are a potential candidate for the treatment of viral infections. Therefore, we developed an EV71-specific conformational MAb with high in vitro cross-neutralization activity to heterologous EV71 subgenotypes. The in vivo treatment experiment at different days post-infection indicated that a single treatment of MAb CT11F9 within day 3 post-infection fully protected mice from morbidity and mortality (0% PBS vs. 100% at 10 mg/g per body weight ***P<0.0001). Immunohistochemical and histological analysis confirmed that CT11F9 significantly prohibited EV71 VP1 expression in various tissues and prevented EV71-induced myonecrosis. Moreover, thrice-treatment at day 4, 5, 6 post-infection was associated with an increased survival rate (18.2% single vs. 50% thrice at 20 mg/g per body weight), and the mice recovered from limb paralysis. Competitive ELISA also confirmed that CT11F9-recognized epitopes were immunodominant in humans. In conclusion, MAb CT11F9 is an ideal candidate to be humanized and used in severe EV71 infection.
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页数:7
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