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首页> 外文期刊>Clinical and vaccine immunology: CVI >An Inactivated Ross River Virus Vaccine Is Well Tolerated and Immunogenic in an Adult Population in a Randomized Phase 3 Trial
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An Inactivated Ross River Virus Vaccine Is Well Tolerated and Immunogenic in an Adult Population in a Randomized Phase 3 Trial

机译:在随机3期试验中,灭活的Ross River病毒疫苗在成人人群中具有良好的耐受性和免疫原性

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Ross River virus (RRV) is endemic in Australia and several South Pacific Islands. More than 90,000 cases of RRV disease, which is characterized by debilitating polyarthritis, were reported in Australia in the last 20 years. There is no vaccine available to prevent RRV disease. A phase 3 study was undertaken at 17 sites in Australia to investigate the safety and immunogenicity of an inactivated whole-virus Vero cell culture-derived RRV vaccine in 1,755 healthy younger adults aged 16 to 59 years and 209 healthy older adults aged >= 60 years. Participants received a 2.5-mu g dose of Al(OH)(3)-adjuvanted RRV vaccine, with a second and third dose after 3 weeks and 6 months, respectively. Vaccine-induced RRV-specific neutralizing and total IgG antibody titers were measured after each immunization. Vaccine safety was monitored over the entire study period. The vaccine was safe and well-tolerated after each vaccination. No cases of arthritis resembling RRV disease were reported. The most frequently reported systemic reactions were headache, fatigue, and malaise; the most frequently reported injection site reactions were tenderness and pain. After the third immunization, 91.5% of the younger age group and 76.0% of the older age group achieved neutralizing antibody titers of >= 1:10; 89.1% of the younger age group and 70.9% of the older age group achieved enzyme-linked immunosorbent assay (ELISA) titers of >= 11 PanBio units. A whole-virus Vero cell culture-derived RRV vaccine is well tolerated in an adult population and induces antibody titers associated with protection from RRV disease in the majority of individuals.
机译:罗斯河病毒(RRV)在澳大利亚和几个南太平洋岛屿上是地方性的。在过去的20年中,澳大利亚报道了澳大利亚有90,000多例RRV疾病,其特征是使人衰弱的多关节炎。没有可预防RRV疾病的疫苗。在澳大利亚的17个地点进行了3阶段研究,以研究1,755名健康的年轻人16至59岁的健康年轻成年人,且209名健康的老年人> 60岁> 60岁的健康年轻人,研究全病毒细胞培养衍生的RRV疫苗的安全性和免疫原性。 。参与者分别在3周零6个月后分别接受了2.5 mu G剂量的Al(OH)(3)(3)(3)剂,第二次和第三剂。每次免疫后测量疫苗诱导的RRV特异性中和和总IgG抗体滴度。在整个研究期间,都监测了疫苗安全性。每次疫苗接种后,该疫苗安全且耐受性良好。没有报告类似于RRV疾病的关节炎病例。最常见的系统反应是头痛,疲劳和不适。最常报告的注射部位反应是压痛和疼痛。第三次免疫接种后,年龄段的91.5%和年龄较大的年龄组的76.0%的中和抗体滴度> = 1:10;年轻年龄段的89.1%和年龄较大的年龄组的70.9%获得了酶联免疫吸附测定法(ELISA)的滴度为> = 11 Panbio单位。在成年人口中,全病毒细胞培养衍生的RRV疫苗具有很好的耐受性,并诱导大多数个体中与RRV疾病的保护相关的抗体滴度。

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