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Meningococcal quadrivalent (Serogroups A, C, W135 and Y) tetanus toxoid conjugate vaccine (Nimenrix?)

机译:脑膜炎球菌四价(A,C,W135和Y血清群)破伤风类毒素结合疫苗(Nimenrix?)

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Nimenrix? (MenACWY-TT) is a quadrivalent meningococcal conjugate vaccine, comprising the polysaccharide serogroups A, C, W135 and Y, and tetanus toxoid (TT) as carrier protein. It is the first quadrivalent vaccine (administered as a single dose) to be approved in Europe for active immunization of individuals aged ≥12 months against invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W135 and Y.Administration of a single dose of Nimenrix? elicited a strong immune response against all four vaccine serogroups in healthy toddlers aged 12-23 months, children and adolescents aged 2-17 years and adults aged 18-55 years in randomized, multicentre, phase III trials. In toddlers, Nimenrix? was noninferior to Meningitec? in terms of seroresponse rates against meningococcal serogroup C 42 days post-vaccination. In children, adolescents and adults, Nimenrix? was noninferior to Mencevax? in terms of vaccination response rates against all four serogroups 1 month post-vaccination. Furthermore, several phase II studies and a phase III trial showed that the immune response elicited by Nimenrix? in all age groups persisted for 7-42 months after the primary vaccination (when evaluated by rabbit serum bactericidal activity), with the vaccine also inducing immune memory in toddlers. In addition, several randomized, multicentre, phase III, noninferiority trials showed that when coadministered with other childhood vaccines or a seasonal flu vaccine, the immunogenicity of Nimenrix? or that of the coadministered vaccine was generally not altered.Nimenrix? was generally well tolerated in all age groups whether administered as a single vaccine or coadministered with other routine vaccines. The incidence of grade 3 local or systemic solicited adverse events during the first 4 days following vaccination and of serious adverse events over an extended follow-up period of up to 6 months was low (<4.5%).Although protective effectiveness and longer-term persistence studies are required, current evidence suggests that Nimenrix?, administered as a single dose, provides a valuable vaccination option for the prevention of meningococcal disease across a broad age group, including children as young as 12 months.
机译:Nimenrix? (MenACWY-TT)是一种四价脑膜炎球菌结合疫苗,包含多糖血清群A,C,W135和Y,以及破伤风类毒素(TT)作为载体蛋白。这是在欧洲被批准用于对年龄≥12个月的个体进行主动免疫以抵抗由脑膜炎奈瑟氏球菌血清群A,C,W135和Y引起的侵袭性脑膜炎球菌疾病的第一批四价疫苗(单剂)。 Nimenrix?在一项随机,多中心,III期试验中,在12-23个月大的健康幼儿,2-17岁的儿童和青少年以及18-55岁的成年人中,针对所有四种疫苗血清群均引起了强烈的免疫反应。在幼儿中,Nimenrix?不亚于Meningitec?接种后42天针对C型脑膜炎球菌血清群的血清反应率。在儿童,青少年和成人中,Nimenrix吗?不亚于Mencevax?接种后1个月对所有四个血清群的疫苗接种应答率。此外,一些II期研究和III期试验表明,Nimenrix引起的免疫应答是?在所有年龄组中,初次接种疫苗后持续7-42个月(通过兔血清杀菌活性评估),该疫苗还可以诱导幼儿的免疫记忆。此外,一些随机,多中心,III期非劣效性试验表明,与其他儿童疫苗或季节性流感疫苗同时使用时,Nimenrix的免疫原性?或通常并用的疫苗没有改变。无论是作为单一疫苗施用还是与其他常规疫苗共同施用,其在所有年龄段的耐受性通常都很好。在接种疫苗后的前4天发生3级局部或全身性不良事件的发生率以及在长达6个月的延长随访期内发生严重不良事件的发生率较低(<4.5%)。持续性研究是必需的,目前的证据表明,Nimenrix?以单剂量给药,为广泛年龄段的儿童,包括12个月大的儿童,提供了预防脑膜炎球菌疾病的有价值的疫苗选择。

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