首页> 外文期刊>Journal of Infectious Diseases >Protection of Rhesus Monkeys against Dengue Virus Challenge after Tetravalent Live Attenuated Dengue Virus Vaccination
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Protection of Rhesus Monkeys against Dengue Virus Challenge after Tetravalent Live Attenuated Dengue Virus Vaccination

机译:四价实时减毒登革热疫苗接种后恒河猴对登革热病毒攻击的保护

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Rhesus monkeys develop viremia after dengue virus (DENV) inoculation and have been used as an animal model to study DENV infection and DENV vaccine candidates. We evaluated, in this model, the protective efficacy of a live attenuated tetravalent DENV vaccine (TDV) candidate against parenteral challenge with parental near-wild-type DENV strains. Twenty monkeys were vaccinated with TDV at 0 and 1 month, and 20 unvaccinated monkeys served as controls. Vaccinated animals and their controls were inoculated with 103–104 pfu of challenge virus 4.5 months after the second vaccination. Primary vaccination resulted in 95%, 100%, 70%, and 15% seroconversion to DENV serotypes 1, 2, 3, and 4 (DENV-1, -2, -3, and -4), respectively. After the second vaccination, the seropositivity rates were 100%, 100%, 90%, and 70%, respectively. Vaccination with TDV resulted in complete protection against viremia from DENV-2 challenge and in 80%, 80%, and 50% protection against challenge with DENV-1, -3, and -4, respectively. Our results suggest that the TDV can elicit protective immunity against all 4 DENV serotypes. Interference among the 4 vaccine viruses may have resulted in decreased antibody responses to DENV-3 and -4, which would require reformulation or dose optimization to minimize this interference during testing of the vaccine in humans
机译:恒河猴接种登革热病毒(DENV)后会发生病毒血症,已被用作研究DENV感染和DENV候选疫苗的动物模型。在该模型中,我们评估了减毒活四价DENV疫苗(TDV)候选物对亲本近野生型DENV株的肠胃外攻击的防护功效。在0和1个月时,给20只猴子接种了TDV疫苗,并将20只未接种的猴子用作对照。第二次疫苗接种后4.5个月,向接种的动物及其对照组接种10 3 –10 4 pfu挑战病毒。初次接种疫苗分别导致95%,100%,70%和15%的血清学转化为DENV血清型1、2、3和4(DENV-1,-2,-3和-4)。第二次接种后,血清阳性率分别为100%,100%,90%和70%。用TDV疫苗接种可完全防御DENV-2攻击的病毒血症,分别具有80%,80%和50%的DENV-1,-3和-4攻击保护。我们的结果表明TDV可以引发针对所有4种DENV血清型的保护性免疫。四种疫苗病毒之间的干扰可能导致针对DENV-3和-4的抗体反应降低,这需要重新配制或优化剂量,以在人体中测试疫苗期间将这种干扰降至最低

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