Using siRNA in prophylactic and therapeutic regimens against SARS coronavirus in rhesus macaque

被引:363
作者
Li, BJ
Tang, QQ
Cheng, D
Qin, C
Xie, FY
Wei, Q
Xu, J
Liu, YJ
Zheng, BJ
Woodle, MC
Zhong, NS
Lu, PY
机构
[1] Intradigm Corp, Rockville, MD 20852 USA
[2] Sun Yatsen Univ, Biotechnol Res Ctr, Guangzhou, Peoples R China
[3] Minist Educ State, Key Lab Gene Engn, Guangzhou, Peoples R China
[4] Guangzhou Top Genom Ltd, Guangzhou, Peoples R China
[5] Chinese Acad Med Sci, Inst Lab Anim Sci, Beijing 100037, Peoples R China
[6] Peking Union Med Coll, Beijing, Peoples R China
[7] Univ Hong Kong, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[8] Guangzhou Inst Resp Dis, Guangzhou, Peoples R China
关键词
D O I
10.1038/nm1280
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Development of therapeutic agents for severe acute respiratory syndrome ( SARS) viral infection using short interfering RNA ( siRNA) inhibitors exemplifies a powerful new means to combat emerging infectious diseases. Potent siRNA inhibitors of SARS coronavirus ( SCV) in vitro were further evaluated for efficacy and safety in a rhesus macaque ( Macaca mulatta) SARS model using clinically viable delivery while comparing three dosing regimens. Observations of SARS- like symptoms, measurements of SCV RNA presence and lung histopathology and immunohistochemistry consistently showed siRNA- mediated anti- SARS efficacy by either prophylactic or therapeutic regimens. The siRNAs used provided relief from SCV infection - induced fever, diminished SCV viral levels and reduced acute diffuse alveoli damage. The 10 - 40 mg/ kg accumulated dosages of siRNA did not show any sign of siRNA- induced toxicity. These results suggest that a clinical investigation is warranted and illustrate the prospects for siRNA to enable a massive reduction in development time for new targeted therapeutic agents.
引用
收藏
页码:944 / 951
页数:8
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