Reason Donald, Liberato Justine, Sun Jinying, Keitel Wendy, Zhou Jianhui
Children's Hospital Oakland Research Institute, 5700 Martin Luther King Jr. Way, Oakland, CA 94609, USA.
Infect Immun. 2009 May;77(5):2030-5. doi: 10.1128/IAI.01254-08. Epub 2009 Feb 17.
Protective antigen (PA) is the cell surface recognition unit of the binary anthrax toxin system and the primary immunogenic component in both the current and proposed "next-generation" anthrax vaccines. Several studies utilizing animal models have indicated that PA-specific antibodies, acquired by either active or passive immunization, are sufficient to protect against infection with Bacillus anthracis. To investigate the human antibody response to anthrax immunization, we have established a large panel of human PA-specific monoclonal antibodies derived from multiple individuals vaccinated with the currently approved anthrax vaccine BioThrax. We have determined that although these antibodies bind PA in standard binding assays such as enzyme-linked immunosorbent assay, Western blotting, capture assays, and dot blots, less than 25% are capable of neutralizing lethal toxin (LT) in vitro. Nonneutralizing antibodies also fail to neutralize toxin when present in combination with other nonneutralizing paratopes. Although neutralizing antibodies recognize determinants throughout the PA monomer, they are significantly less common among those paratopes that bind to the immunodominant amino-terminal portion of the molecule. These findings demonstrate that PA binding alone is not sufficient to neutralize LT and suggest that for an antibody to effectively block PA-mediated toxicity, it must bind to PA such that one of the requisite toxin functions is disrupted. A vaccine design strategy that directed a higher percentage of the antibody response toward neutralizing epitopes may result in a more efficacious vaccine for the prevention of anthrax infection.
保护性抗原(PA)是二元炭疽毒素系统的细胞表面识别单位,也是当前和提议的“下一代”炭疽疫苗中的主要免疫原性成分。多项利用动物模型的研究表明,通过主动或被动免疫获得的PA特异性抗体足以预防炭疽芽孢杆菌感染。为了研究人类对炭疽疫苗接种的抗体反应,我们建立了大量源自接种目前已获批的炭疽疫苗BioThrax的多个个体的人类PA特异性单克隆抗体。我们已经确定,尽管这些抗体在标准结合试验如酶联免疫吸附测定、蛋白质印迹、捕获测定和斑点印迹中能与PA结合,但体外能够中和致死毒素(LT)的不到25%。非中和抗体与其他非中和抗原决定部位同时存在时也无法中和毒素。尽管中和抗体识别PA单体上的各个决定部位,但在与分子免疫显性氨基末端部分结合的那些抗原决定部位中,它们的数量明显较少。这些发现表明,仅PA结合不足以中和LT,这表明对于一种抗体要有效阻断PA介导的毒性,它必须与PA结合,从而破坏毒素的一种必需功能。一种将更高比例的抗体反应导向中和表位的疫苗设计策略可能会产生一种预防炭疽感染更有效的疫苗。