Childrens Hospital, Dr. Horst Schmidt Clinic, Ludwig-Erhard-Straße 100, 65199 Wiesbaden, Germany.
Eur J Pediatr. 2013 May;172(5):601-12. doi: 10.1007/s00431-012-1924-0. Epub 2013 Jan 11.
In Europe, the introduction of monovalent meningococcal serogroup C (MenC) conjugate vaccines has resulted in a significant decline in MenC invasive disease. However, given the potential for strain evolution and increasing travel to areas of high endemicity, protection against additional serogroups is needed. In this study, the immunogenicity, measured by a serum bactericidal activity assay using rabbit complement (rSBA), and the safety of a quadrivalent meningococcal serogroups A, C, W-135 and Y tetanus toxoid conjugate vaccine (MenACWY-TT) were compared to that of a licensed monovalent MenC conjugate vaccine (MenC-CRM₁₉₇) in children 2-10 years of age. Children were randomised (3:1) to receive a single dose of either MenACWY-TT or MenC-CRM₁₉₇. Non-inferiority of the immunogenicity of MenACWY-TT versus MenC-CRM₁₉₇ in terms of rSBA-MenC vaccine response was demonstrated. Exploratory analyses suggested that rSBA-MenC geometric mean titres adjusted for pre-vaccination titres were lower in children vaccinated with MenACWY-TT compared to MenC-CRM₁₉₇. Nevertheless, at 1 month post-vaccination, ≥99.3 % of the children who received MenACWY-TT had rSBA titres ≥1:128 for each of the four vaccine serogroups, which is the more conservative correlate of protection. The reactogenicity and safety profile of MenACWY-TT was clinically acceptable and no serious adverse events considered related to vaccination were reported throughout the study.
When administered to European school-age children, MenACWY-TT has a clinically acceptable safety profile and, when compared with MenC-CRM₁₉₇, the potential to broaden protection against meningococcal disease caused by serogroups A, W-135 and Y while maintaining protection against MenC. This study has been registered at www.clinicaltrials.gov NCT00674583.
在欧洲,单价脑膜炎奈瑟菌 C 群(MenC)结合疫苗的引入导致了 MenC 侵袭性疾病的显著下降。然而,鉴于菌株进化的可能性以及前往高流行地区旅行的增加,需要针对其他血清群提供保护。在这项研究中,通过使用兔补体的血清杀菌活性测定(rSBA)测量了四价脑膜炎奈瑟菌血清群 A、C、W-135 和 Y 破伤风类毒素结合疫苗(MenACWY-TT)的免疫原性,并与已批准的单价脑膜炎奈瑟菌 C 结合疫苗(MenC-CRM₁₉₇)进行了比较,研究对象为 2-10 岁的儿童。儿童以 3:1 的比例随机接受单剂量的 MenACWY-TT 或 MenC-CRM₁₉₇。在 rSBA-MenC 疫苗反应方面,证明了 MenACWY-TT 的免疫原性与 MenC-CRM₁₉₇相比非劣效。探索性分析表明,接种 MenACWY-TT 的儿童的 rSBA-MenC 几何平均滴度校正预接种前的滴度后,与 MenC-CRM₁₉₇相比,滴度较低。然而,在接种后 1 个月,接受 MenACWY-TT 的儿童中有≥99.3%的儿童针对四种疫苗血清群的 rSBA 滴度≥1:128,这是更保守的保护相关指标。MenACWY-TT 的反应原性和安全性特征是可以接受的,在整个研究过程中,没有报告任何严重不良事件被认为与接种有关。
在欧洲学龄儿童中,MenACWY-TT 具有可接受的临床安全性,与 MenC-CRM₁₉₇相比,有潜力扩大针对血清群 A、W-135 和 Y 引起的脑膜炎奈瑟病的保护,同时保持对 MenC 的保护。本研究已在 www.clinicaltrials.gov 注册,编号为 NCT00674583。