Am J Trop Med Hyg. 2012 Oct;87(4):743-753. doi: 10.4269/ajtmh.2012.12-0004. Epub 2012 Aug 13.
The immunogenicity and safety of three novel host-range vaccines containing deletions in the transmembrane domain of dengue virus serotype 2 (DV2) E glycoprotein were evaluated in African green monkeys. The shorter transmembrane domains are capable of functionally spanning an insect but not a mammalian cell membrane, resulting in production of viral mutants that have reduced infectivity in mammalian hosts but efficient growth in insect cells. Groups of four monkeys received one dose each of test vaccine candidate with no booster immunization. After immunization, levels of viremia produced by each vaccine were determined by infectious center assay. Vaccine recipient immune response to wild-type DV2 challenge was measured on Day 57 by enzyme-linked immunosorbent assay and plaque reduction neutralization test. Two vaccines, DV2ΔGVII and DV2G460P, generated neutralizing antibody in the range of 700-900 50% plaque reduction neutralization test units. All three vaccine strains decreased the length of viremia by at least two days. No safety concerns were identified.
三种新型宿主范围疫苗在非洲绿猴中进行了免疫原性和安全性评估,这些疫苗均含有登革病毒血清型 2(DV2)E 糖蛋白跨膜域缺失。较短的跨膜域能够在功能上跨越昆虫细胞膜,但不能跨越哺乳动物细胞膜,从而产生病毒突变体,这些突变体在哺乳动物宿主中的感染性降低,但在昆虫细胞中生长效率更高。每组四只猴子分别接受一剂试验候选疫苗,没有加强免疫。免疫后,通过感染中心测定法测定每种疫苗产生的病毒血症水平。在第 57 天,通过酶联免疫吸附试验和蚀斑减少中和试验测定疫苗接种者对野生型 DV2 攻击的免疫反应。两种疫苗,DV2ΔGVII 和 DV2G460P,产生了中和抗体,范围在 700-900 50%蚀斑减少中和试验单位。三种疫苗株均将病毒血症的持续时间至少缩短了两天。未发现安全问题。