The yellow fever 17D virus as a platform for new live attenuated vaccines

被引:36
作者
Bonaldo, Myrna C. [1 ]
Sequeira, Patricia C. [1 ]
Galler, Ricardo [2 ]
机构
[1] Fiocruz MS, IOC, Lab Biol Mol Flavivirus, Rio De Janeiro, Brazil
[2] Fiocruz MS, Inst Tecnol Imunobiol, Rio De Janeiro, Brazil
关键词
Yellow Fever; 17D virus-vaccines-immune responses-expression; vector-insertion; sites-live; recombinant virus; TETRAVALENT DENGUE VACCINE; T-CELL RESPONSES; WEST-NILE-VIRUS; INDIAN RHESUS MACAQUES; HEALTHY-ADULTS; PHASE-II; FLAVIVIRUS INFECTIONS; ENDOPLASMIC-RETICULUM; PROTECTIVE EFFICACY; ENVELOPE PROTEIN;
D O I
10.4161/hv.28117
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
The live-attenuated yellow fever 17D virus is one of the most outstanding human vaccines ever developed. It induces efficacious immune responses at a low production cost with a well-established manufacture process. These advantages make the YF17D virus attractive as a vector for the development of new vaccines. At the beginning of vector development studies, YF17D was genetically manipulated to express other flavivirus prM and E proteins, components of the viral envelope. While these 17D recombinants are based on the substitution of equivalent YF17D genes, other antigens from unrelated pathogens have also been successfully expressed and delivered by recombinant YF17D viruses employing alternative strategies for genetic manipulation of the YF17D genome. Herein, we discuss these strategies in terms of possibilities of single epitope or larger sequence expression and the main properties of these replication-competent viral platforms.
引用
收藏
页码:1256 / 1265
页数:10
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