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首页> 外文期刊>Clinical and vaccine immunology: CVI >Recombinant protective antigen anthrax vaccine improves survival when administered as a postexposure prophylaxis countermeasure with antibiotic in the New Zealand white rabbit model of inhalation anthrax
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Recombinant protective antigen anthrax vaccine improves survival when administered as a postexposure prophylaxis countermeasure with antibiotic in the New Zealand white rabbit model of inhalation anthrax

机译:重组保护抗原炭疽疫苗当管理作为提高生存曝光后预防对策与抗生素在新西兰白兔模型中吸入炭疽热的

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摘要

Inhalation anthrax is a potentially lethal form of disease resulting from exposure to aerosolized Bacillus anthracis spores. Over the last decade, incidents spanning from the deliberate mailing of B. anthracis spores to incidental exposures in users of illegal drugs have highlighted the importance of developing new medical countermeasures to protect people who have been exposed to "anthrax spores" and are at risk of developing disease. The New Zealand White rabbit (NZWR) is a well-characterized model that has a pathogenesis and clinical presentation similar to those seen in humans. This article reports how the NZWR model was adapted to evaluate postexposure prophylaxis using a recombinant protective antigen (rPA) vaccine in combination with an oral antibiotic, levofloxacin. NZWRs were exposed to multiples of the 50% lethal dose (LD 50) of B. anthracis spores and then vaccinated immediately (day 0) and again on day 7 postexposure. Levofloxacin was administered daily beginning at 6 to 12 h postexposure for 7 treatments. Rabbits were evaluated for clinical signs of disease, fever, bacteremia, immune response, and survival. A robust immune response (IgG anti-rPA and toxin-neutralizing antibodies) was observed in all vaccinated groups on days 10 to 12. Levofloxacin plus either 30 or 100 μg rPA vaccine resulted in a 100% survival rate (18 of 18 per group), and a vaccine dose as low as 10 μg rPA resulted in an 89% survival rate (16 of 18) when used in combination with levofloxacin. In NZWRs that received antibiotic alone, the survival rate was 56% (10 of 18). There was no adverse effect on the development of a specific IgG response to rPA in unchallenged NZWRs that received the combination treatment of vaccine plus antibiotic. This study demonstrated that an accelerated two-dose regimen of rPA vaccine coadministered on days 0 and 7 with 7 days of levofloxacin therapy results in a significantly greater survival rate than with antibiotic treatment alone. Combination of vaccine administration and antibiotic treatment may be an effective strategy for treating a population exposed to aerosolized B. anthracis spores.
机译:吸入炭疽是一种潜在的致命的疾病产生的雾化炭疽杆菌孢子。事件生成的深思熟虑的邮件炭疽杆菌孢子偶然曝光用户非法毒品的强调了开发新医学的重要性对策来保护的人暴露于炭疽孢子”的风险发展疾病。(NZWR)是一个良好的模型发病机制和临床表现相似这些人类。NZWR模型适应评估曝光后预防使用重组结合保护性抗原(战)疫苗口服抗生素,左氧氟沙星。暴露于50%的致死量的倍数(LD炭疽杆菌孢子的50),然后接种疫苗立即(0)天7天曝光后。开始在6到12 h曝光后7治疗方法。疾病的迹象,发热、菌血症、免疫反应,和生存。(免疫球蛋白g anti-rPA和toxin-neutralizing抗体)在所有接种组观察10天吗到12。疫苗导致的存活率(18 100%每组)18,疫苗剂量低至10μg战导致生存率89% (16 18)当与左氧氟沙星结合使用。NZWRs仅接受抗生素治疗,18的存活率为56%(10)。对一个特定的发展产生不良影响免疫球蛋白应对战挑战NZWRs接受疫苗的联合治疗加抗生素。的加速剂治疗方案则疫苗coadministered在0到7天7天的左氧氟沙星治疗效果显著存活率比抗生素单独治疗。可能是一个管理和抗生素治疗治疗人群有效的策略暴露于雾化炭疽杆菌孢子。

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