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:重组保护性抗原炭疽疫苗在新西兰白兔吸入炭疽模型中作为抗生素的暴露后预防对策,可提高生存率

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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 (LD50) 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:吸入炭疽病是由于暴露于雾化的炭疽芽孢杆菌孢子而引起的潜在致命疾病。在过去的十年中,从故意寄送炭疽杆菌孢子到非法吸毒者偶然接触的事件突显了制定新的医疗对策以保护已暴露于“炭疽芽孢”并有感染风险的人的重要性。发展中的疾病。新西兰白兔(NZWR)是一个特征明确的模型,其发病机理和临床表现与人类相似。本文报告了如何使用重组保护性抗原(rPA)疫苗与口服抗生素左氧氟沙星联合使用NZWR模型来评估暴露后预防。 NZWRs暴露于炭疽芽孢杆菌孢子的50%致死剂量(LD 50 )的倍数,然后立即(第0天)和暴露后第7天再次接种。左氧氟沙星每天从暴露后6至12小时开始给药,共7次治疗。评估了兔子的疾病,发烧,菌血症,免疫应答和存活的临床体征。在第10到12天,在所有接种组中均观察到了强大的免疫应答(IgG抗rPA和毒素中和抗体)。左氧氟沙星加30或100μgrPA疫苗的存活率为100%(每18例中有18例)与左氧氟沙星联用时,低至10μgrPA的疫苗剂量可产生89%的存活率(18中的16)。在仅接受抗生素治疗的NZWR中,存活率为56%(18个病例中的10个)。在接受疫苗加抗生素联合治疗的无挑战性NZWR中,对rPA的特异性IgG反应的发展没有不利影响。这项研究表明,在0和7天与左氧氟沙星治疗共7天同时使用rPA疫苗的加速两剂方案,其生存率明显高于单纯抗生素治疗。疫苗接种和抗生素治疗相结合可能是治疗暴露于气溶胶​​化的炭疽芽孢杆菌孢子的种群的有效策略。

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