Immunogenicity and Safety of a Quadrivalent Meningococcal Tetanus Toxoid­-Conjugate Vaccine (MenACYW­-TT) Administered Concomitantly with Pneumococcal Conjugate Vaccine in Healthy Toddlers in the Russian Federation: a Phase III Randomized Study

L. S. Namazova­-Baranova, O. Perminova, T. A. Romanova, V. Romanenko, A. Galustyan, V. Gorodin, I. Osipova, V. Rodnikova, S. Kharit, Y. Kovshirina, V. Anokhin, S. B'chir, D. Neveu, M. Bonaparte, G. Áñez, E. Jordanov, M. S. Dhingra, A. Goldstein
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Abstract

Relevance. Invasive meningococcal disease (IMD) has high morbidity and mortality, with infants and young children among those at greatest risk.Materials & Methods. A phase III, open-­label, randomized study in toddlers aged 12–23 months evaluated the immunogenicity and safety of MenACYW­TT, a tetanus toxoid conjugated vaccine against meningococcal serogroups A, C, W, and Y, when coadministered with paediatric vaccines (measles, mumps and rubella [MMR]; varicella [V] in South Korea and Thailand; 6­in­1 combination vaccine against diphtheria, tetanus, pertussis, polio, hepatitis B and Haemophilus influenzae type b [DTaP­IPVHepB­Hib] in Mexico and pneumococcal conjugate vaccine [PCV13]) in the Russian Federation (NCT03205371). This manuscript reports the outcome of the part of the study conducted in the Russian Federation using PCV13 as the co­administered vaccine. Immunogenicity to each meningococcal serogroup was assessed by serum bactericidal antibody assay using human complement (hSBA) and, for a subset of subjects, baby rabbit complement (rSBA). Vaccine safety profiles were described up to 30 days postvaccination.Results. A total of 1,183 participants were enrolled in the study, out of which 400 were from the Russian Federation. The proportion with seroprotection (hSBA ≥1:8) to each meningococcal serogroup at Day 30 was comparable between the MenACYW­-TT and MenACYW-­TT + PCV13 groups (≥91% and ≥84%, respectively). The safety profiles of MenACYW­-TT and PCV13, when given alone or concomitantly, were generally comparable.Conclusion. Coadministration of MenACYW­-TT with pneumococcal conjugate vaccine in toddlers had no clinically relevant effect on the immunogenicity and safety of any of the vaccines.
四价脑膜炎球菌-破伤风类毒素结合疫苗(MenACYW -TT)与肺炎球菌结合疫苗在俄罗斯联邦健康幼儿中的免疫原性和安全性:一项III期随机研究
的相关性。侵袭性脑膜炎球菌病(IMD)具有很高的发病率和死亡率,其中婴儿和幼儿的风险最大。材料与方法。一项针对12-23月龄幼儿的III期、开放标签、随机研究评估了MenACYW-TT与儿科疫苗(麻疹、腮腺炎和风疹[MMR])共同接种时的免疫原性和安全性,该疫苗是一种针对脑膜炎球菌血清群A、C、W和Y的破伤风类毒素结合疫苗;韩国和泰国的水痘[V];墨西哥的白喉、破伤风、百日咳、脊髓灰质炎、乙型肝炎和乙型流感嗜血杆菌6合1联合疫苗[DTaP-IPVHepB-Hib]和俄罗斯联邦的肺炎球菌结合疫苗[PCV13] (NCT03205371)。本文报告了在俄罗斯联邦使用PCV13作为联合接种疫苗的部分研究结果。采用人补体(hSBA)和一小部分兔补体(rSBA)进行血清杀菌抗体测定,评估对每个脑膜炎球菌血清组的免疫原性。研究人员描述了疫苗接种后30天的安全性。共有1183名参与者参加了这项研究,其中400名来自俄罗斯联邦。在第30天,每个脑膜炎球菌血清组中具有血清保护(hSBA≥1:8)的比例在MenACYW- TT和MenACYW- TT + PCV13组之间具有可比性(分别为≥91%和≥84%)。MenACYW—TT与PCV13单独或合用时的安全性大致相当。幼儿同时使用MenACYW—TT与肺炎球菌结合疫苗对任何疫苗的免疫原性和安全性均无临床相关影响。
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