Wressnigg Nina, van der Velden Maikel V W, Portsmouth Daniel, Draxler Wolfgang, O'Rourke Maria, Richmond Peter, Hall Stephen, McBride William J H, Redfern Andrew, Aaskov John, Barrett P Noel, Aichinger Gerald
Vaccine R&D, Baxter BioScience, Vienna, Austria
Vaccine R&D, Baxter BioScience, Vienna, Austria.
Clin Vaccine Immunol. 2015 Mar;22(3):267-73. doi: 10.1128/CVI.00546-14. Epub 2014 Dec 24.
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-μg 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. (This study is registered at www.clinicaltrials.gov under registration no. NCT01242670.).
罗斯河病毒(RRV)在澳大利亚和几个南太平洋岛屿呈地方性流行。在过去20年里,澳大利亚报告了超过90000例以使人衰弱的多关节炎为特征的RRV疾病病例。目前尚无预防RRV疾病的疫苗。在澳大利亚的17个地点开展了一项3期研究,以调查一种源自Vero细胞培养的灭活全病毒RRV疫苗在1755名16至59岁健康年轻成年人和209名≥60岁健康老年人中的安全性和免疫原性。参与者接受一剂2.5μg含氢氧化铝(Al(OH)(3))佐剂的RRV疫苗,分别在3周和6个月后接种第二剂和第三剂。每次免疫后测量疫苗诱导的RRV特异性中和抗体和总IgG抗体滴度。在整个研究期间监测疫苗安全性。每次接种疫苗后,该疫苗均安全且耐受性良好。未报告类似RRV疾病的关节炎病例。最常报告的全身反应是头痛、疲劳和不适;最常报告的注射部位反应是压痛和疼痛。第三次免疫后,91.5%的年轻年龄组和76.0%的老年年龄组中和抗体滴度≥1:10;89.1%的年轻年龄组和70.9%的老年年龄组酶联免疫吸附测定(ELISA)滴度≥11个PanBio单位。一种源自Vero细胞培养的全病毒RRV疫苗在成年人群中耐受性良好,并能在大多数个体中诱导出与预防RRV疾病相关的抗体滴度。(本研究已在www.clinicaltrials.gov注册,注册号为NCT01242670。)