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婴幼儿四价脑膜炎球菌多糖 CRM 结合疫苗的免疫原性和安全性。

Immunogenicity and safety of a quadrivalent meningococcal polysaccharide CRM conjugate vaccine in infants and toddlers.

机构信息

Centro de Desarrollo de Proyectos Avanzados, Córdoba, Argentina.

Centro de Estudios en Infectologia Pediátrica (CEIP), Cali, Colombia.

出版信息

Int J Infect Dis. 2014 Sep;26:22-30. doi: 10.1016/j.ijid.2014.03.1390. Epub 2014 Jun 26.

DOI:10.1016/j.ijid.2014.03.1390
PMID:24980467
Abstract

OBJECTIVES

This phase III study assessed the safety and immunogenicity of MenACWY-CRM, a quadrivalent meningococcal conjugate vaccine, administered with routine vaccines starting at 2 months of age.

METHODS

Healthy infants received MenACWY-CRM in a two- or three-dose primary infant series plus a single toddler dose. In addition, a two-dose toddler catch-up series was evaluated. Immune responses to MenACWY-CRM were assessed for serum bactericidal activity with human complement (hSBA). Reactogenicity and safety results were collected systematically.

RESULTS

After a full infant/toddler series or two-dose toddler catch-up series, MenACWY-CRM elicited immune responses against the four serogroups in 94-100% of subjects. Noninferiority of the two- versus three-dose MenACWY-CRM infant dosing regimen was established for geometric mean titers for all serogroups. Following the three-dose infant primary series, 89-98% of subjects achieved an hSBA ≥ 8 across all serogroups. Immune responses to concomitant routine vaccines given with MenACWY-CRM were noninferior to responses to routine vaccines alone, except for pertactin after the two-dose infant series. Noninferiority criteria were met for all concomitant antigens after the three-dose infant series.

CONCLUSIONS

MenACWY-CRM vaccination regimens in infants and toddlers were immunogenic and well tolerated. No clinically meaningful effects of concomitant administration with routine infant and toddler vaccines were observed.

摘要

目的

本 III 期研究评估了 MenACWY-CRM(一种四价脑膜炎球菌结合疫苗)的安全性和免疫原性,该疫苗与常规疫苗联合使用,于 2 月龄开始接种。

方法

健康婴儿接受 MenACWY-CRM 两剂或三剂基础婴儿系列接种加一剂幼儿单剂加强接种。此外,还评估了两剂幼儿补种系列接种。采用人源补体(hSBA)检测血清杀菌活性来评估对 MenACWY-CRM 的免疫应答。系统收集了不良反应和安全性结果。

结果

在完成婴儿/幼儿系列或两剂幼儿补种系列接种后,MenACWY-CRM 在 94%-100%的受试者中引发了针对四个血清群的免疫应答。两剂与三剂 MenACWY-CRM 婴儿接种方案的非劣效性在所有血清群的几何平均滴度上得到确立。在完成三剂婴儿基础系列接种后,89%-98%的受试者在所有血清群中达到 hSBA≥8。与单独使用常规疫苗相比,与 MenACWY-CRM 同时接种的常规疫苗的免疫应答无差异,但在两剂婴儿系列接种后,对 pertactin 的免疫应答除外。在完成三剂婴儿系列接种后,所有伴随抗原均符合非劣效性标准。

结论

婴儿和幼儿的 MenACWY-CRM 疫苗接种方案具有免疫原性且耐受性良好。与常规婴儿和幼儿疫苗同时接种未观察到有临床意义的影响。

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