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首页> 外文期刊>BioDrugs: Clinical immunotherapeutics, biopharmaceuticals, and gene therapy >Meningococcal quadrivalent (serogroups A, C, w135, and y) conjugate vaccine (Menveo): in adolescents and adults.
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Meningococcal quadrivalent (serogroups A, C, w135, and y) conjugate vaccine (Menveo): in adolescents and adults.

机译:脑膜炎球菌四价(A,C,w135和y血清群)结合疫苗(Menveo):在青少年和成人中。

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Menveo is a quadrivalent meningococcal polysaccharide conjugate vaccine containing the four Neisseria meningitidis capsular polysaccharides, A, C, W135, and Y, each conjugated to the mutant diphtheria toxin, known as crossreactive material 197 (CRM(197)). Administration of a single dose of the Menveo vaccine elicited a strong immune response against all four vaccine serogroups in adolescents and adults in randomized, single- or multicenter, phase II or III trials. In adolescents, Menveo was generally more immunogenic against vaccine serogroups than the polysaccharide conjugate vaccine Menactra or the unconjugated polysaccharide vaccine Menomune, in terms of seroresponse and/or seroprotection rates and geometric mean titers (GMTs) 1 month post-vaccination in two phase II or III studies. In two phase III trials in adults aged 19-55 years, the immunogenicity of Menveo was generally noninferior or superior to that of Menactra against all four vaccine serogroups, with regard to seroresponse/seroprotection rates, and GMTs 1 month after vaccination. Moreover, an exploratory arm of one of these studies suggested Menveo was at least as immunogenic as Menomune in adults aged 56-65 years. Longer term, the immunogenicity of Menveo persisted for 12-22 months post-vaccination in the adolescent studies, with the vaccine generally remaining at least as immunogenic as Menactra or Menomune. Coadministration of Menveo with a combined tetanus, reduced diphtheria, and acellular pertussis (Tdap) vaccine or Tdap and human papillomavirus vaccines generally did not affect the immunogenicity of these vaccines in adolescents and young adults in two additional randomized, single- or multicenter, phase III studies. The tolerability profile of Menveo was generally similar to that of the comparator vaccines Menactra or Menomune in adults and adolescents, and few Menveo recipients experienced serious adverse events within 30 days or 6 months post-vaccination.
机译:Menveo是一种四价脑膜炎球菌多糖结合疫苗,包含四种脑膜炎奈瑟氏球菌荚膜多糖A,C,W135和Y,每种均与突变型白喉毒素结合,被称为交叉反应物质197(CRM(197))。在随机,单中心或多中心的II期或III期试验中,单剂Menveo疫苗的施用引起了针对青少年和成人中所有四个疫苗血清群的强烈免疫反应。在青少年中,就两个阶段或两个阶段的疫苗接种后1个月的血清反应和/或血清保护率和几何平均滴度(GMT)而言,与多糖结合疫苗Menactra或非结合多糖疫苗Menomune相比,Menveo对疫苗血清群的免疫原性更高III研究。在两项针对19-55岁成年人的III期试验中,就血清反应/血清保护率和疫苗接种1个月后的GMT而言,Menveo对所有四个疫苗血清组的免疫原性通常均不低于Menactra。此外,其中一项研究的探索性研究表明,在56-65岁的成年人中,孟韦至少具有与孟诺一样的免疫原性。从长远来看,在青少年研究中,孟韦的免疫原性在接种疫苗后持续了12-22个月,疫苗通常至少保持与孟纳斯特拉或梅诺蒙一样的免疫原性。 Menveo与破伤风,白喉减少和无细胞百日咳(Tdap)组合疫苗或Tdap和人乳头瘤病毒疫苗的联合给药通常不会在另外两个随机的单中心或多中心III期中影响青少年和年轻人中这些疫苗的免疫原性学习。 Menveo在成人和青少年中的耐受性特征通常与比较疫苗Menactra或Menomune相似,很少有Menveo接受者在接种疫苗后30天内或6个月内出现严重不良事件。

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