| Literature DB >> 17931120 |
Deyan Luo1, Bing Ni, Guangyu Zhao, Zhengcai Jia, Lili Zhou, Marek Pacal, Liangyan Zhang, Songle Zhang, Li Xing, Zhihua Lin, Li Wang, Jintao Li, Yunfei Liang, Xinfu Shi, Tingting Zhao, Liyun Zou, Yuzhang Wu, Xiliang Wang.
Abstract
To warrant potential clinical testing, the equine anti-severe acute respiratory syndrome coronavirus (SARS-CoV) F(ab')(2) requires evaluation in as many animal models as possible. In this study, we established a new animal model, the Chinese hamster, susceptible to SARS-CoV infection. SARS-CoV could propagate effectively and sustain high levels for 1 wk in animal lungs. All animals were protected from SARS-CoV infection in preventive settings. Further, when used therapeutically this antibody led to an approximately 4-log(10) decrease in viral burden in infected animal lungs. The pathological changes in lungs correlated closely with the dose of antibody administered. The excellent preventive and therapeutic roles of equine anti-SARS-CoV F(ab')(2) in several animal models, including the novel Chinese hamster model described in this study, have provided exciting data concerning its potential clinical study.Entities:
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Year: 2007 PMID: 17931120 DOI: 10.1089/vim.2007.0038
Source DB: PubMed Journal: Viral Immunol ISSN: 0882-8245 Impact factor: 2.257