Apt Doris, Raviprakash Kanakatte, Brinkman Alice, Semyonov Andrey, Yang Shumin, Skinner Craig, Diehl Lori, Lyons Richard, Porter Kevin, Punnonen Juha
Maxygen Inc., Human Therapeutics, 515 Galveston Drive, Redwood City, CA 94063, USA.
Vaccine. 2006 Jan 16;24(3):335-44. doi: 10.1016/j.vaccine.2005.07.100. Epub 2005 Aug 10.
We employed DNA shuffling and screening technologies to develop a single recombinant dengue envelope (E) antigen capable of inducing neutralizing antibodies against all four antigenically distinct dengue serotypes. By DNA shuffling of codon-optimized dengue 1-4 E genes, we created a panel of novel chimeric clones expressing C-terminal truncated E antigens that combined epitopes from all four dengue serotypes. DNA vaccines encoding these novel chimeras induced multivalent T cell and neutralizing antibody responses against all four dengue serotypes in mice. By contrast, a mixture of four unshuffled, parental DNA vaccines failed to produce tetravalent neutralizing antibodies in mice. The neutralizing antibody titers for some of these antigens could be further improved by extending the sequences to express full-length pre-membrane and envelope proteins. The chimeric antigens also protected mice against a lethal dengue-2 virus challenge. These data demonstrate that DNA shuffling and associated screening can lead to the selection of multi-epitope antigens against closely related dengue virus serotypes and suggest a broad utility for these technologies in optimizing vaccine antigens.
我们采用DNA改组和筛选技术来开发一种单一的重组登革病毒包膜(E)抗原,该抗原能够诱导针对所有四种抗原性不同的登革病毒血清型产生中和抗体。通过对密码子优化的登革病毒1 - 4型E基因进行DNA改组,我们创建了一组表达C末端截短E抗原的新型嵌合克隆,这些抗原组合了来自所有四种登革病毒血清型的表位。编码这些新型嵌合体的DNA疫苗在小鼠体内诱导了针对所有四种登革病毒血清型的多价T细胞和中和抗体反应。相比之下,四种未改组的亲本DNA疫苗混合物未能在小鼠体内产生四价中和抗体。通过延长序列以表达全长前膜和包膜蛋白,其中一些抗原的中和抗体效价可进一步提高。这些嵌合抗原还能保护小鼠免受致死性登革病毒2型的攻击。这些数据表明,DNA改组及相关筛选能够筛选出针对密切相关的登革病毒血清型的多表位抗原,并表明这些技术在优化疫苗抗原方面具有广泛的应用价值。