Division of Infectious and Immunological Diseases, Department of Paediatrics, University of British Columbia Vancouver, BC, Canada.
Front Immunol. 2013 Apr 2;4:81. doi: 10.3389/fimmu.2013.00081. eCollection 2013.
The success of the World Health Organization recommended "Expanded Program of Immunization" (EPI) and similar regional or national programs has been astounding. However, infectious threats currently not covered by these programs continue to infect millions of infants around the world. Furthermore, many infants do not receive existing vaccines either on time or for the required number of doses to provide optimal protection. Nor do all infants around the world develop the same protective immune response to the same vaccine. As a result approximately three million infants die every year from vaccine preventable infections. To tackle these issues, new vaccines need to be developed as well as existing ones made easier to administer. This requires identification of age-optimized vaccine schedules and formulations. In order to be most effective this approach will need to take population-based differences in response to vaccines and adjuvants into account. This review summarizes what is currently known about differences between populations around the world in the innate immune response to existing as well as new and promising vaccine adjuvants.
世界卫生组织推荐的“扩大免疫规划”(EPI)和类似的区域或国家计划的成功令人震惊。然而,目前这些计划未涵盖的传染病威胁仍在继续感染全球数百万婴儿。此外,许多婴儿要么没有按时接种,要么没有接种所需的剂量,从而无法获得最佳保护。而且,全球并非所有婴儿对相同的疫苗都产生相同的保护性免疫反应。因此,每年约有 300 万婴儿死于可通过疫苗预防的感染。为了解决这些问题,不仅需要开发新疫苗,还要使现有疫苗更容易管理。这就需要确定最佳年龄的疫苗接种时间表和配方。为了达到最佳效果,这种方法需要考虑到人群对疫苗和佐剂的反应存在差异。这篇综述总结了目前已知的全球不同人群对现有以及新的和有前途的疫苗佐剂的固有免疫反应的差异。