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Therapy and Long-Term Prophylaxis of Vaccinia Virus Respiratory Infections in Mice with an Adenovirus-Vectored Interferon Alpha (mDEF201)

机译:腺病毒载体干扰素α(mDEF201)对小鼠痘苗病毒呼吸道感染的治疗和长期预防

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摘要

An adenovirus 5 vector encoding for mouse interferon alpha, subtype 5 (mDEF201) was evaluated for efficacy against lethal vaccinia virus (WR strain) respiratory infections in mice. mDEF201 was administered as a single intranasal treatment either prophylactically or therapeutically at doses of 106 to 108 plaque forming units/mouse. When the prophylactic treatment was given at 56 days prior to infection, it protected 90% of animals from death (100% protection for treatments given between 1–49 days pre-infection), with minimal weight loss occurring during infection. Surviving animals re-challenged with virus 22 days after the primary infection were protected from death, indicating that mDEF201 did not compromise the immune response against the initial infection. Post-exposure therapy was given between 6–24 h after vaccinia virus exposure and protection was afforded by a 108 dose of mDEF201 given at 24 h, whereas a 107 dose was effective up to 12 h. Comparisons were made of the ability of mDEF201, given either 28 or 1 day prior to infection, to inhibit tissue virus titers and lung infection parameters. Lung, liver, and spleen virus titers were inhibited to nearly the same extent by either treatment, as were lung weights and lung hemorrhage scores (indicators of pneumonitis). Lung virus titers were significantly (>100-fold) lower than in the placebo group, and the other infection parameters in mDEF201 treated mice were nearly at baseline. In contrast, viral titers and lung infection parameters were high in the placebo group on day 5 of the infection. These results demonstrate the long-acting prophylactic and treatment capacity of mDEF201 to combat vaccinia virus infections.
机译:评价了编码小鼠干扰素α5亚型(mDEF201)的腺病毒5载体对小鼠致命牛痘病毒(WR株)呼吸道感染的功效。预防性或治疗性地将mDEF201作为单一的鼻内治疗剂,剂量为10 6 至10 8 斑块形成单位/小鼠。当在感染前56天进行预防性治疗时,它可以保护90%的动物免于死亡(感染前1–49天之间给予100%的保护),并且在感染过程中体重减轻最小。初次感染后22天再次受到病毒攻击的存活动物被保护免于死亡,这表明mDEF201不会损害针对初始感染的免疫反应。牛痘病毒暴露后6–24 h进行暴露后治疗,并在24 h给予10 8 剂量的mDEF201给予保护,而10 7 剂量给予保护长达12小时有效。比较了感染前28天或1天给予mDEF201抑制组织病毒滴度和肺部感染参数的能力。两种治疗方法对肺,肝和脾脏病毒滴度的抑制程度几乎相同,肺重量和肺出血分数(肺炎的指标)也是如此。肺病毒滴度明显低于安慰剂组(> 100倍),mDEF201治疗小鼠的其他感染参数几乎处于基线水平。相反,在感染的第5天,安慰剂组的病毒滴度和肺部感染参数较高。这些结果证明了mDEF201对抗牛痘病毒感染的长效预防和治疗能力。

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