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Protection from infection with severe acute respiratory syndrome coronavirus in a Chinese hamster model by equine neutralizing F(ab')2.

Identifieur interne : 003627 ( Main/Exploration ); précédent : 003626; suivant : 003628

Protection from infection with severe acute respiratory syndrome coronavirus in a Chinese hamster model by equine neutralizing F(ab')2.

Auteurs : Deyan Luo [République populaire de Chine] ; 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

Source :

RBID : pubmed:17931120

Descripteurs français

English descriptors

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.

DOI: 10.1089/vim.2007.0038
PubMed: 17931120


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">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.</div>
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