Viret Jean-François, Dietrich Guido, Favre Didier
Berna Biotech Ltd., Rehhagstrasse 79, CH-3018 Berne, Switzerland.
Vaccine. 2004 Jun 23;22(19):2457-69. doi: 10.1016/j.vaccine.2003.12.033.
The development of live attenuated vaccines, allowing for the safe and effective immunisation at mucosal surfaces, is a strategy of great interest for vaccinologists. The main advantage of this approach over conventional parenteral vaccines is the induction of strong mucosal immune responses, allowing targeting of the pathogen at the initial point of contact with the host. Further advantages include the ease of administration, high acceptance by vaccines, and relatively low production costs. Finally, well-characterised, safe and immunogenic vaccine strains are well suited as vectors for the mucosal delivery of foreign vaccine antigens and of DNA vaccines. However, such vaccines, when based on or containing genetically modified organisms (GMOs), are facing new and specific regulatory hurdles, particularly regarding the potential risks for humans and the environment. In this contribution we address selected aspects of the risk assessment of live attenuated bacterial vaccines covered in the course of the registration of vaccine strain CVD 103-HgR as a recombinant live oral vaccine against cholera.
减毒活疫苗的研发能够在黏膜表面实现安全有效的免疫接种,这是疫苗学家极为关注的一种策略。与传统的注射用疫苗相比,这种方法的主要优势在于能够诱导强烈的黏膜免疫反应,从而在病原体与宿主的初始接触点对其进行靶向攻击。其他优势还包括易于给药、疫苗接受度高以及生产成本相对较低。最后,特征明确、安全且具有免疫原性的疫苗菌株非常适合作为载体,用于黏膜递送外源疫苗抗原和DNA疫苗。然而,这类基于或含有转基因生物(GMO)的疫苗正面临新的特定监管障碍,尤其是在对人类和环境的潜在风险方面。在本论文中,我们探讨了疫苗菌株CVD 103-HgR作为重组口服霍乱活疫苗注册过程中所涉及的减毒活细菌疫苗风险评估的某些方面。