Structure-based antigen design: a strategy for next generation vaccines

被引:123
作者
Dormitzer, Philip R. [1 ]
Ulmer, Jeffrey B. [1 ]
Rappuoli, Rino [1 ]
机构
[1] Novartis Vaccines & Diagnost Inc, Cambridge, MA 02139 USA
关键词
D O I
10.1016/j.tibtech.2008.08.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Vaccine design is progressing from empiricism towards the increasingly rational presentation of the targets of protective immunity. Nevertheless, most current vaccine antigens are essentially the native macromolecules of pathogens. These molecules are adapted to evade, not induce, immunity. High resolution structures reveal the electrostatic surfaces recognized by neutralizing antibodies and the architectures underlying these surfaces, thereby identifying which substructures must be left intact and which can be changed to optimize biochemical and immunologic performance. Armed with detailed structural information, we can engineer optimized antigens that are more stable, homogeneous, and efficiently produced, making immunization more practical and affordable. Understanding the structural basis for immunogenicity and immunodominance will allow us to improve vaccine efficacy and broaden the range of vaccine-preventable diseases.
引用
收藏
页码:659 / 667
页数:9
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