Kochel T J, Raviprakash K, Hayes C G, Watts D M, Russell K L, Gozalo A S, Phillips I A, Ewing D F, Murphy G S, Porter K R
Virology Program, Naval Medical Research Center, 8901 Wisconsin Avenue, 20889-5607, Bethesda, MD, USA.
Vaccine. 2000 Jul 15;18(27):3166-73. doi: 10.1016/s0264-410x(00)00105-5.
A DNA vaccine that expresses the premembrane/membrane (prM) and envelope (E) genes of dengue virus serotype-1 was tested for immunogenicity and protection against dengue-1 virus challenge in Aotus nancymae monkeys. The vaccine, in 1 mg doses, was administered intradermally (i.d.) to three monkeys and intramuscularly (i.m.) to three others. For controls, a 1 mg dose of vector DNA was administered i.d. to two monkeys and i.m. to one. All animals were primed and then boosted at one and five months post priming. Sera were collected monthly and analyzed for dengue-1 antibodies by enzyme linked immunosorbent assay (ELISA) and plaque reduction neutralization test (PRNT). Dengue-1 antibodies were detectable in the sera from i.d. and i.m. vaccine inoculated animals one month after the first boost and peaked one month after the second boost. The antibody levels from sera of animals that received the vaccine via the i.d. route were twice those from sera of animals that received the vaccine via the i.m. route. Six months after the second boost all inoculated and two naive monkeys were challenged with 1.25x10(4) plaque forming units (PFU) of dengue-1 virus. Two vaccine immunized animals were protected from viremia while the others showed a reduction in viremia. The mean days of viremia were 1 and 1.3 for the animals that were immunized with the vaccine via the i.d. or i.m. route, respectively vs 4 and 2 mean days of viremia in the animals inoculated with control DNA. Naive animals were viremic for an average of 4 days. All of the three control monkeys that received control DNA inoculum by either the i.d. or i.m. route had an intermittent viremia pattern with one or more negative days interspersed between the positive days. This pattern was not observed in any of the vaccine recipients or the naïve control monkeys. These results demonstrate that DNA immunization is a promising approach for the development of dengue vaccines and that A. nancymae monkeys are suitable for dengue vaccine trials.
一种表达登革热病毒1型前膜/膜(prM)和包膜(E)基因的DNA疫苗,在南美白狨猴中进行了免疫原性测试以及针对登革热1型病毒攻击的保护性测试。该疫苗以1毫克剂量,对三只猴子进行皮内注射,对另外三只进行肌肉注射。作为对照,对两只猴子进行皮内注射1毫克剂量的载体DNA,对一只进行肌肉注射。所有动物均先进行初次免疫,然后在初次免疫后的1个月和5个月进行加强免疫。每月采集血清,通过酶联免疫吸附测定(ELISA)和蚀斑减少中和试验(PRNT)分析登革热1型抗体。在初次加强免疫1个月后,皮内和肌肉注射疫苗的动物血清中可检测到登革热1型抗体,并在第二次加强免疫1个月后达到峰值。通过皮内途径接种疫苗的动物血清中的抗体水平是通过肌肉途径接种疫苗的动物血清中抗体水平的两倍。第二次加强免疫6个月后,所有接种疫苗的动物和两只未接种的猴子接受了1.25×10⁴蚀斑形成单位(PFU)的登革热1型病毒攻击。两只接种疫苗的动物免受病毒血症影响,而其他动物的病毒血症有所减轻。通过皮内或肌肉途径接种疫苗的动物的病毒血症平均天数分别为1天和1.3天,而接种对照DNA的动物的病毒血症平均天数为4天和2天。未接种的动物平均病毒血症持续4天。通过皮内或肌肉途径接受对照DNA接种物的三只对照猴子均呈现间歇性病毒血症模式,在阳性天数之间穿插有一个或多个阴性天数。在任何接种疫苗的动物或未接种的对照猴子中均未观察到这种模式。这些结果表明,DNA免疫是开发登革热疫苗的一种有前景的方法,并且南美白狨猴适用于登革热疫苗试验。