Helios Dr. Horst Schmidt Kliniken Wiesbaden, Wiesbaden, Germany.
Vaccine Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Hum Vaccin Immunother. 2022 Nov 30;18(5):2052657. doi: 10.1080/21645515.2022.2052657. Epub 2022 Apr 21.
MenACYW-TT (MenQuadfi®) is a quadrivalent meningococcal tetanus toxoid conjugate vaccine licensed in Europe for use in individuals ≥12 months. This study assessed whether serogroup C immune responses with MenACYW-TT were at least non-inferior, or superior, to those of quadrivalent meningococcal ACWY (MCV4-TT; Nimenrix®) and monovalent meningococcal C (MenC-TT; NeisVac-C®) vaccines in toddlers (12-23 months). In this modified, double-blind Phase III study (NCT03890367), 701 toddlers received one dose of MenACYW-TT (n = 230), MCV4-TT (n = 232) or MenC-TT (n = 239). Serum bactericidal assays with human (hSBA) and baby rabbit (rSBA) complement were used to measure anti-meningococcal serogroup C antibodies at baseline and 30 days post-vaccination. A sequential statistical approach was used for primary and secondary objectives. For the primary objectives, superiority of serogroup C was assessed in terms of hSBA seroprotection rates (defined as titers ≥1:8) and GMTs for MenACYW-TT compared to MCV4-TT, and rSBA GMTs compared to MenC-TT. The safety of all vaccines within 30 days post-vaccination was described. When administered as a single dose to meningococcal vaccine-naïve healthy toddlers the superiority of the MenACYW-TT serogroup C immune response versus MCV4-TT was demonstrated for hSBA GMTs (ratio 16.3 [12.7-21.0]) and seroprotection (difference 10.43% [5.68-16.20]); and versus MenC-TT in terms of rSBA GMTs (ratio 1.32 [1.06-1.64]). The safety profiles of a single dose of MenACYW-TT, MCV4-TT and MenC-TT were similar. In meningococcal vaccine-naïve toddlers, MenACYW-TT induced superior immune responses to serogroup C versus MCV4-TT in terms of hSBA seroprotection and GMTs and versus MenC-TT in terms of rSBA GMTs.
MenACYW-TT(MenQuadfi®)是一种四价脑膜炎奈瑟菌破伤风类毒素结合疫苗,在欧洲获准用于 12 个月及以上人群。本研究旨在评估 MenACYW-TT 对血清群 C 的免疫应答是否至少不劣于,或优于四价脑膜炎奈瑟菌 ACWY(MCV4-TT;Nimenrix®)和单价脑膜炎奈瑟菌 C(MenC-TT;NeisVac-C®)疫苗,用于评估 12-23 个月龄的幼儿。在这项改良的、双盲的 III 期研究(NCT03890367)中,701 名幼儿接受了 1 剂 MenACYW-TT(n=230)、MCV4-TT(n=232)或 MenC-TT(n=239)。使用人血清杀菌试验(hSBA)和兔血清杀菌试验(rSBA)来测量基线和接种后 30 天的抗脑膜炎奈瑟菌血清群 C 抗体。采用顺序统计学方法评估主要和次要目标。对于主要目标,评估了 MenACYW-TT 血清群 C 的优势,其依据是 hSBA 血清保护率(定义为滴度≥1:8)和与 MCV4-TT 相比的 GMT,以及与 MenC-TT 相比的 rSBA GMT。描述了接种后 30 天内所有疫苗的安全性。当作为单剂接种给脑膜炎奈瑟菌疫苗初免的健康幼儿时,MenACYW-TT 血清群 C 免疫应答优于 MCV4-TT,hSBA GMT(比值 16.3[12.7-21.0])和血清保护率(差异 10.43%[5.68-16.20]);与 MenC-TT 相比,rSBA GMT(比值 1.32[1.06-1.64])。MenACYW-TT、MCV4-TT 和 MenC-TT 的单剂安全性概况相似。在脑膜炎奈瑟菌疫苗初免的幼儿中,与 MCV4-TT 相比,MenACYW-TT 诱导了针对血清群 C 的更优免疫应答,hSBA 血清保护率和 GMT 更高,与 MenC-TT 相比,rSBA GMT 更高。