Savransky Vladimir, Shearer Jeffry D, Gainey Melicia R, Sanford Daniel C, Sivko Gloria S, Stark Gregory V, Li Na, Ionin Boris, Lacy Michael J, Skiadopoulos Mario H
Emergent BioSolutions Inc., 300 Professional Drive, Gaithersburg, MD 20879, USA.
Battelle, Columbus, OH 43201, USA.
Vaccine. 2017 Sep 5;35(37):4952-4959. doi: 10.1016/j.vaccine.2017.07.076. Epub 2017 Jul 31.
The anthrax vaccine candidate AV7909 is being developed as a next generation vaccine for a post-exposure prophylaxis (PEP) indication against anthrax. AV7909 consists of the Anthrax Vaccine Adsorbed (AVA, BioThrax®) bulk drug substance adjuvanted with the immunostimulatory oligodeoxynucleotide (ODN) compound, CPG 7909. The addition of CPG 7909 to AVA enhances both the magnitude and the kinetics of antibody responses in animals and human subjects, making AV7909 a suitable next-generation vaccine for use in a PEP setting. The studies described here provide initial information on AV7909-induced toxin-neutralizing antibody (TNA) levels associated with the protection of animals from lethal Bacillus anthracis challenge. Guinea pigs or nonhuman primates (NHPs) were immunized on Days 0 and 28 with various dilutions of AV7909, AVA or a saline or Alhydrogel+CPG 7909 control. Animals were challenged via the inhalational route with a lethal dose of aerosolized B. anthracis (Ames strain) spores and observed for clinical signs of disease and mortality. The relationship between pre-challenge serum TNA levels and survival following challenge was determined in order to calculate a threshold TNA level associated with protection. Immunisation with AV7909 induced a rapid, highly protective TNA response in guinea pigs and NHPs. Surprisingly, the TNA threshold associated with a 70% probability of survival for AV7909 immunized animals was substantially lower than the threshold which has been established for the licensed AVA vaccine. The results of this study suggest that the TNA threshold of protection against anthrax could be modified by the addition of an immune stimulant such as CPG 7909 and that the TNA levels associated with protection may be vaccine-specific.
炭疽候选疫苗AV7909正在被开发作为一种用于炭疽暴露后预防(PEP)适应症的下一代疫苗。AV7909由吸附炭疽疫苗(AVA,BioThrax®)原料药与免疫刺激寡脱氧核苷酸(ODN)化合物CPG 7909佐剂组成。向AVA中添加CPG 7909可增强动物和人类受试者抗体反应的强度和动力学,使AV7909成为适用于PEP环境的下一代疫苗。此处描述的研究提供了关于AV7909诱导的毒素中和抗体(TNA)水平的初步信息,这些水平与保护动物免受致死性炭疽芽孢杆菌攻击有关。在第0天和第28天,用不同稀释度的AV7909、AVA或生理盐水或氢氧化铝凝胶+CPG 7909对照对豚鼠或非人灵长类动物(NHP)进行免疫。通过吸入途径用致死剂量的雾化炭疽芽孢杆菌(Ames菌株)孢子对动物进行攻击,并观察疾病的临床症状和死亡率。确定攻击前血清TNA水平与攻击后存活之间的关系,以计算与保护相关的TNA阈值。用AV7909免疫可在豚鼠和NHP中诱导快速、高度保护性的TNA反应。令人惊讶的是,与接受AV7909免疫的动物70%存活概率相关的TNA阈值大大低于已获许可的AVA疫苗所确定的阈值。本研究结果表明,添加免疫刺激剂如CPG 7909可改变针对炭疽的TNA保护阈值,且与保护相关的TNA水平可能具有疫苗特异性。