Fritzell B
Chiron Vaccines Clinical Research, Amsterdam, The Netherlands.
Dev Biol Stand. 1998;95:181-8.
The duplication of usually large-scale efficacy trials to generalise the clinical database of a new vaccine to other populations can be avoided by bridging studies. Immunogenicity data can easily be used to extrapolate efficacy results when the immune response correlates with vaccine induced immunity. In the absence of such a correlate of protection, the bridging process will be more controversial. Previous experiences should be valuable in identifying the factors, either ethnic or vaccine-related that may have an influence on vaccine efficacy. The probability that such a factor is associated with a clinically significant difference in efficacy is critical to the decision to conduct a bridging study. Bridging studies are designed to demonstrate equivalent immunogenicity i.e. exclude a clinically significant difference in the immune response between the population in whom efficacy was shown and the population to whom those efficacy results are extrapolated.
通过桥接研究可以避免通常大规模的疗效试验重复进行,以便将新疫苗的临床数据库推广到其他人群。当免疫反应与疫苗诱导的免疫力相关时,免疫原性数据可轻松用于推断疗效结果。在缺乏这种保护相关性的情况下,桥接过程将更具争议性。以往的经验对于识别可能影响疫苗疗效的因素(无论是种族因素还是疫苗相关因素)具有重要价值。这种因素与疗效上具有临床显著差异相关的可能性对于决定是否开展桥接研究至关重要。桥接研究旨在证明等效的免疫原性,即排除在显示出疗效的人群与将疗效结果外推应用的人群之间免疫反应存在临床显著差异的情况。