Huang Bruce, Xie Tao, Rotstein David, Fang Hui, Frucht David M
Division of Biotechnology Review and Research II, Office of Biotechnology Products, Office of Product Quality, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD 20993-0002, USA.
Division of Compliance, Center for Veterinary Medicine, U.S. Food and Drug Administration, Rockville, MD 20855, USA.
Toxins (Basel). 2015 Sep 29;7(10):3960-76. doi: 10.3390/toxins7103960.
The principal portal for anthrax infection in natural animal outbreaks is the digestive tract. Enteric exposure to anthrax, which is difficult to detect or prevent in a timely manner, could be exploited as an act of terror through contamination of human or animal food. Our group has developed a novel animal model of gastrointestinal (GI) anthrax for evaluation of disease pathogenesis and experimental therapeutics, utilizing vegetative Bacillus anthracis (Sterne strain) administered to A/J mice (a complement-deficient strain) by oral gavage. We hypothesized that a humanized recombinant monoclonal antibody (mAb) * that neutralizes the protective antigen (PA) component of B. anthracis lethal toxin (LT) and edema toxin (ET) could be an effective treatment. Although the efficacy of this anti-anthrax PA mAb has been shown in animal models of inhalational anthrax, its activity in GI infection had not yet been ascertained. We hereby demonstrate that passive immunotherapy with anti-anthrax PA mAb, administered at the same time as gastrointestinal exposure to B. anthracis, prevents lethal sepsis in nearly all cases (>90%), while a delay of up to forty-eight hours in treatment still greatly reduces mortality following exposure (65%). Moreover, passive immunotherapy protects against enteric invasion, associated mucosal injury and subsequent dissemination by gastrointestinal B. anthracis, indicating that it acts to prevent the initial stages of infection. * Expired raxibacumab being cycled off the Strategic National Stockpile; biological activity confirmed by in vitro assay.
在自然发生的动物炭疽疫情中,主要的感染途径是消化道。肠道接触炭疽杆菌很难及时检测或预防,可能会被恐怖分子利用,通过污染人类或动物食物来实施恐怖行为。我们团队开发了一种新型的胃肠道炭疽动物模型,用于评估疾病发病机制和实验性治疗方法,该模型通过给A/J小鼠(一种补体缺陷型品系)经口灌胃接种炭疽杆菌(斯特恩株)的营养体。我们假设,一种能中和炭疽杆菌致死毒素(LT)和水肿毒素(ET)中保护性抗原(PA)成分的人源化重组单克隆抗体(mAb)可能是一种有效的治疗方法。尽管这种抗炭疽PA mAb在吸入性炭疽动物模型中已显示出疗效,但其在胃肠道感染中的活性尚未确定。我们在此证明,在胃肠道接触炭疽杆菌的同时给予抗炭疽PA mAb进行被动免疫治疗,几乎在所有情况下(>90%)都能预防致死性败血症,而治疗延迟长达48小时仍能大大降低接触后的死亡率(65%)。此外,被动免疫治疗可预防肠道入侵、相关的黏膜损伤以及随后胃肠道炭疽杆菌的传播,这表明它能预防感染的初始阶段。*过期的raxibacumab正从国家战略储备中淘汰;体外试验确认其生物活性。