Jiangsu Provincial Center for Diseases Control and Prevention, Nanjing, China.
Department of Public Health, Southeast University, Nanjing, China.
Hum Vaccin Immunother. 2019;15(12):2952-2959. doi: 10.1080/21645515.2019.1627816. Epub 2019 Jul 26.
: This exploratory study aimed to assess the immunogenicity and safety of 1 and 2 doses of meningococcal serogroups A and C tetanus toxoid-conjugate vaccine (MenAC-TT) in toddles.: Healthy participants aged 12-23 months were randomized into two groups to receive 1 or 2 doses of the tested vaccine. The interval was 28 days between two doses. Blood samples were collected at day 0 before the immunization and day 28 post-each dose. Safety observation was conducted during 28 days after each vaccination. Serious adverse event (SAE) was conducted throughout 6 month observation period.: Overall 301 toddles were vaccinated. Twenty-eight days post full-course vaccination, ≥97.20% toddles had titers ≥1:8 and ≥81.48% had titers ≥1:128 for MenA and MenC in the two schedules groups. There were no significant differences between the two schedule groups for each titer thresholds and serogroups. Up to month 12 post the first dose, titers ≥1:8 and 1:128 were declined to 71.32-80.83% and 26.67-57.85% for each meningococcal serogroups. Most adverse reactions (ARs) were mild or moderate, and the incidence of grade 3 ARs was below 3.33%. The incidence of redness was significantly higher in the two doses group than that in the one dose group, in terms of grade 1 and grade 2 were higher. No SAEs were considered causally related to vaccination.: The MenAC-TT showed similarly safety and immunogenicity profile in toddles with two schedules. It will be more important to provide the data for formulating appropriate immunization strategies in different age groups in China.
这项探索性研究旨在评估 1 剂和 2 剂脑膜炎球菌 A 群和 C 群结合型破伤风类毒素疫苗(MenAC-TT)在幼儿中的免疫原性和安全性。
健康的 12-23 月龄参与者被随机分为两组,分别接受 1 剂或 2 剂受试疫苗。两剂之间的间隔为 28 天。在免疫前第 0 天和第 28 天采集血样。在每次接种后 28 天进行安全性观察。严重不良事件(SAE)在整个 6 个月的观察期内进行。
总体上有 301 名幼儿接种了疫苗。在全程接种后 28 天,两剂方案组中,≥97.20%的幼儿针对 MenA 和 MenC 的抗体滴度均≥1:8,≥81.48%的幼儿抗体滴度均≥1:128。在每个滴度阈值和血清型组中,两剂方案组之间没有显著差异。在第 1 剂后 12 个月,针对每个脑膜炎球菌血清型,抗体滴度≥1:8 和 1:128 下降至 71.32-80.83%和 26.67-57.85%。大多数不良反应(ARs)为轻度或中度,3 级 ARs 的发生率低于 3.33%。在两剂方案组中,1 级和 2 级的红斑发生率明显高于一剂方案组。没有 SAE 被认为与接种有关。
MenAC-TT 在两剂方案中具有相似的安全性和免疫原性特征。在中国不同年龄组制定适当的免疫策略时,提供数据将更为重要。