Ferrari Marilyn E, Hermanson Gary, Rolland Alain
Vical Inc, 10390 Pacific Center Court, San Diego, CA 92121, USA.
Curr Opin Mol Ther. 2004 Oct;6(5):506-12.
Over 120 years ago, Pasteur and Greenfield developed an in vitro procedure for producing a live-attenuated Bacillus anthracis bacterial culture capable of protecting livestock from anthrax disease. Since then, anthrax has become one of the best characterized bacterial pathogens with regard to mechanism of toxicity and vaccine development. Most developments have used live-attenuated strains, bacterial supernatants or protein subunit approaches. Recently, novel plasmid DNA (pDNA) approaches to a safe and effective anthrax vaccine have been proposed. This review summarizes the history of anthrax, the need for new vaccines and recent developments in pDNA-based vaccines, leading to the initiation of a human phase I clinical trial in a significantly shorter timeframe than in traditional vaccine development.
120多年前,巴斯德和格林菲尔德开发了一种体外程序,用于生产能够保护牲畜免受炭疽病侵害的减毒活炭疽芽孢杆菌培养物。从那时起,就毒性机制和疫苗开发而言,炭疽已成为特征最明显的细菌病原体之一。大多数进展都采用了减毒活菌株、细菌上清液或蛋白质亚基方法。最近,有人提出了新型质粒DNA(pDNA)方法来开发安全有效的炭疽疫苗。本综述总结了炭疽的历史、对新疫苗的需求以及基于pDNA的疫苗的最新进展,从而在比传统疫苗开发短得多的时间内启动了一项人体I期临床试验。