Rappuoli Rino, Bottomley Matthew J, D'Oro Ugo, Finco Oretta, De Gregorio Ennio
GlaxoSmithKline Vaccines S.r.l., 53100 Siena, Italy
GlaxoSmithKline Vaccines S.r.l., 53100 Siena, Italy.
J Exp Med. 2016 Apr 4;213(4):469-81. doi: 10.1084/jem.20151960. Epub 2016 Mar 28.
Traditionally, vaccines have been developed by cultivating infectious agents and isolating the inactivated whole pathogen or some of its purified components. 20 years ago, reverse vaccinology enabled vaccine discovery and design based on information deriving from the sequence of microbial genomes rather than via the growth of pathogens. Today, the high throughput discovery of protective human antibodies, sequencing of the B cell repertoire, and the increasing structural characterization of protective antigens and epitopes provide the molecular and mechanistic understanding to drive the discovery of novel vaccines that were previously impossible. We are entering a "reverse vaccinology 2.0" era.
传统上,疫苗是通过培养感染因子并分离灭活的全病原体或其一些纯化成分来研发的。20年前,反向疫苗学使疫苗的发现和设计基于微生物基因组序列所获得的信息,而非通过病原体的培养。如今,保护性人类抗体的高通量发现、B细胞库测序以及保护性抗原和表位的结构表征不断增加,为推动发现以前不可能的新型疫苗提供了分子和机制方面的理解。我们正在进入一个“反向疫苗学2.0”时代。