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首页> 外文期刊>Japanese journal of infectious diseases >Immunogenicity and Safety of a Two-Dose Series of a Meningococcal (Groups A, C, W, and Y) Polysaccharide Diphtheria Toxoid Conjugate Vaccine (Men-ACWY-D) in Healthy Japanese Adults
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Immunogenicity and Safety of a Two-Dose Series of a Meningococcal (Groups A, C, W, and Y) Polysaccharide Diphtheria Toxoid Conjugate Vaccine (Men-ACWY-D) in Healthy Japanese Adults

机译:两剂量系列的免疫原性和安全性的脑膜炎球菌(A,C,W和Y)多糖毒素白糖毒素偶氮偶联疫苗(男性ACWY-D)在健康的日本成年人中

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摘要

The quadrivalent meningococcal polysaccharide diphtheria toxoid conjugate vaccine (Men-ACWY-D) has been licensed for use in Japan since 2014. An earlier registration study demonstrated the immunogenicity of a single dose in Japanese adults, wherein the immunogenicity against serogroup C was the lowest. The determination of the potential to increase the serogroup C response with a second dose was, therefore, of interest. This study (NCT02591290) evaluated the safety and immunogenicity of two doses administered 8 weeks apart to 60 healthy Japanese adults aged 20–55 years. Blood samples were collected at 28–35 days after vaccination. Immunogenicity endpoints included seroprotection and seroconversion rates. Safety assessments included systemic adverse events (AEs), non-serious AEs, and serious AEs. Fifty-eight participants (96.7%) completed the study. The seroprotection rates for serogroups A, C, W, and Y before vaccination were 76.8%, 26.8%, 26.8%, and 50.0%, respectively, increasing to 100%, 83.9%, 91.1%, and 96.4% and 100%, 92.9%, 94.6%, and 94.6%, respectively, after two doses. The seroconversion rates for the four serogroups were 100%, 93.8%, 97.1%, and 94.1%, respectively, after the first dose, and 100%, 96.9%, 100%, and 100%, respectively, after the second. The increase between the doses was insignificant, and there were no safety concerns. The two-dose series was well tolerated; however, the clinical benefits of a second dose within 8 weeks seemed to be low.
机译:自2014年以来,四肢脑膜炎球菌多糖白糖白糖毒素疫苗(MEN-ACWY-D)已被许可用于日本。早期的注册研究证明了日本成年人中单剂量的免疫原性,其中对血群C的免疫原性是最低的。因此,测定增加血群C与第二剂量的反应的潜力是感兴趣的。本研究(NCT02591290)评估了两次施用8周的两种剂量的安全性和免疫原性,与60岁的20-55岁的健康日本成年人。在疫苗接种后28-35天收集血样。免疫原性终点包括SEROOLOCTION和SEROCONVERSION率。安全评估包括全身不良事件(AES),非严重AES和严重AES。五十八名参与者(96.7%)完成了这项研究。疫苗接种前的血清浦解率A,C,W和Y分别为76.8%,26.8%,26.8%和50.0%,增加到100%,83.9%,91.1%和96.4%和100%,92.9分别在两剂量后分别为94.6%和94.6%。四种血清聚类的血清转化率分别为100%,93.8%,97.1%和94.1%,分别在第二种剂量之后,100%,96.9%,100%和100%。剂量之间的增加是微不足道的,并且没有安全顾虑。双剂量系列耐受良好;然而,8周内第二剂的临床益处似乎是低的。

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