Department of Veterinary Pathobiology, Texas A&M University College Station, TX 77843, USA.
Front Cell Infect Microbiol. 2013 May 16;3:17. doi: 10.3389/fcimb.2013.00017. eCollection 2013.
Vaccination is the most important approach to counteract infectious diseases. Thus, the development of new and improved vaccines for existing, emerging, and re-emerging diseases is an area of great interest to the scientific community and general public. Traditional approaches to subunit antigen discovery and vaccine development lack consideration for the critical aspects of public safety and activation of relevant protective host immunity. The availability of genomic sequences for pathogenic Brucella spp. and their hosts have led to development of systems-wide analytical tools that have provided a better understanding of host and pathogen physiology while also beginning to unravel the intricacies at the host-pathogen interface. Advances in pathogen biology, host immunology, and host-agent interactions have the potential to serve as a platform for the design and implementation of better-targeted antigen discovery approaches. With emphasis on Brucella spp., we probe the biological aspects of host and pathogen that merit consideration in the targeted design of subunit antigen discovery and vaccine development.
疫苗接种是对抗传染病最重要的方法。因此,开发针对现有、新兴和重现传染病的新型和改进疫苗是科学界和公众关注的重点领域。传统的亚单位抗原发现和疫苗开发方法缺乏对公共安全和相关保护性宿主免疫激活的重要方面的考虑。致病性布鲁氏菌及其宿主的基因组序列的可用性,促使开发了系统范围的分析工具,这些工具提供了对宿主和病原体生理学的更好理解,同时也开始揭示宿主-病原体界面的复杂性。病原体生物学、宿主免疫学和宿主-试剂相互作用的进展有可能成为设计和实施更有针对性的抗原发现方法的平台。我们重点探讨了布鲁氏菌属,研究了宿主和病原体的生物学方面,这些方面在针对亚单位抗原发现和疫苗开发的靶向设计中值得考虑。