Towards an evidence based approach for the development of adjuvanted vaccines

被引:82
作者
O'Hagan, Derek T. [1 ]
Friedland, Leonard R. [2 ]
Hanon, Emmanuel [3 ]
Didierlaurent, Arnaud M. [3 ]
机构
[1] GSK Vaccines, 14200 Shady Grove Rd, Rockville, MD 20850 USA
[2] GSK Vaccines, 5 Crescent Dr, Philadelphia, PA USA
[3] GSK Vaccines, Rue Inst 89, B-1330 Rixensart, Belgium
关键词
T-CELL RESPONSES; DENDRITIC CELLS; IMMUNE-RESPONSES; MOLECULAR SIGNATURES; TLR7; AGONIST; SYSTEMS; ACTIVATION; INNATE; IDENTIFICATION; GENERATION;
D O I
10.1016/j.coi.2017.07.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the last two decades, several vaccines formulated with a new generation of adjuvants have been licensed or approved to target diseases such as influenza, hepatitis B, cervical cancer, and malaria. These new generation adjuvants appear to work by delivering a localized activation signal to the innate immune system, which in turn promotes antigen-specific adaptive immunity. Advances in understanding of the innate immune system together with high-throughput discovery of synthetic immune potentiators are now expanding the portfolio of new generation adjuvants available for evaluation. Meanwhile, omics and systems biology are providing molecular benchmarks or signatures to assess vaccine safety and effectiveness. This accumulating knowledge and experience raises the prospect that the future selection of the right antigen/adjuvant combination can be more evidence based and can speed up the clinical development program for new adjuvanted vaccines.
引用
收藏
页码:93 / 102
页数:10
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