Ohanjanian Lernik, Remy Kenneth E, Li Yan, Cui Xizhong, Eichacker Peter Q
National Institutes of Health, Clinical Center, Critical Care Medicine Department , Building 10, Room 2C145, Bethesda, MD 20892 , USA +1 301 402 2914 ; +1 301 402 1213 ;
Expert Opin Investig Drugs. 2015;24(7):851-65. doi: 10.1517/13543784.2015.1041587. Epub 2015 Apr 28.
Sepsis with Bacillus anthracis infection has a very high mortality rate despite appropriate antibiotic and supportive therapies. Over the past 15 years, recent outbreaks in the US and in Europe, coupled with anthrax's bioterrorism weapon potential, have stimulated efforts to develop adjunctive therapies to improve clinical outcomes. Since lethal toxin and edema toxin (LT and ET) make central contributions to the pathogenesis of B. anthracis, these have been major targets in this effort.
Here, the authors review different investigative biopharmaceuticals that have been recently identified for their therapeutic potential as inhibitors of LT or ET. Among these inhibitors are two antibody preparations that have been included in the Strategic National Stockpile (SNS) and several more that have reached Phase I testing. Presently, however, many of these candidate agents have only been studied in vitro and very few tested in bacteria-challenged models.
Although a large number of drugs have been identified as potential therapeutic inhibitors of LT and ET, in most cases their testing has been limited. The use of the two SNS antibody therapies during a large-scale exposure to B. anthracis will be difficult. Further testing and development of agents with oral bioavailability and relatively long shelf lives should be a focus for future research.
尽管采取了适当的抗生素治疗和支持性治疗,但炭疽芽孢杆菌感染引起的败血症死亡率仍非常高。在过去15年中,美国和欧洲最近爆发的疫情,再加上炭疽作为生物恐怖主义武器的潜在威胁,促使人们努力开发辅助疗法以改善临床结果。由于致死毒素和水肿毒素(LT和ET)在炭疽芽孢杆菌的发病机制中起核心作用,因此它们一直是这项工作的主要目标。
在此,作者综述了最近被确定具有作为LT或ET抑制剂的治疗潜力的不同研究性生物制药。这些抑制剂中包括两种已被纳入国家战略储备(SNS)的抗体制剂,以及另外几种已进入I期试验的制剂。然而,目前这些候选药物大多仅在体外进行了研究,很少在细菌攻击模型中进行测试。
尽管已确定大量药物为LT和ET的潜在治疗抑制剂,但在大多数情况下,它们的测试都很有限。在大规模接触炭疽芽孢杆菌期间使用两种SNS抗体疗法将很困难。未来研究应重点关注进一步测试和开发具有口服生物利用度和相对较长保质期的药物。