Institute for Antiviral Research, Department of Animal, Dairy and Veterinary Science, 5600 Old Main Hill, Logan, Utah State University, Logan, UT 84322, USA.
Antiviral Res. 2011 Jan;89(1):75-82. doi: 10.1016/j.antiviral.2010.11.007. Epub 2010 Nov 18.
Interferons (IFNs) are a first line of defense against viral infection. Herein we describe the use of an adenovirus vectored mouse IFN alpha gene (mDEF201) as a prophylactic and treatment countermeasure in a SARS-CoV-infected BALB/c mouse model. Complete survival protection was observed in mice given a single dose of mDEF201 administered intranasally 1, 3, 5, 7, or 14 days prior to lethal SARS-CoV challenge (p<0.001), and body weights of these treated mice were unaffected by the challenge. In addition, low doses of mDEF201 protected lungs in a dose dependent manner as measured by a reduction in gross pathology. Intranasal treatment with mDEF201 ranging from 10(6) to 10(8)PFU significantly protected mice against a lethal SARS-CoV infection in a dose dependent manner up to 12h post infection (p<0.001). The data suggest that mDEF201 is a new class of antiviral agent further development as treatment for SARS-CoV infections.
干扰素 (IFNs) 是抵抗病毒感染的第一道防线。在此,我们描述了一种腺病毒载体的小鼠 IFNα 基因 (mDEF201) 作为一种预防和治疗 SARS-CoV 感染的 BALB/c 小鼠模型的对策。在 SARS-CoV 攻击前 1、3、5、7 或 14 天给予单剂量鼻腔内给予 mDEF201 的小鼠观察到完全的存活保护 (p<0.001),并且这些治疗小鼠的体重不受攻击的影响。此外,低剂量的 mDEF201 通过减少大体病理学测量,以剂量依赖的方式保护肺部。从 10(6)到 10(8)PFU 的鼻腔内给予 mDEF201 治疗在感染后 12 小时内以剂量依赖的方式显著保护小鼠免受致死性 SARS-CoV 感染 (p<0.001)。数据表明 mDEF201 是一种新的抗病毒药物,进一步开发为治疗 SARS-CoV 感染的药物。