Clinical Research Division, Research Institute for Tropical Medicine , Alabang, Muntinlupa City, Philippines.
Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.
Hum Vaccin Immunother. 2020 Jun 2;16(6):1272-1279. doi: 10.1080/21645515.2020.1744363. Epub 2020 May 13.
A previous phase 3, randomized, multicenter study showed the immunogenicity of a primary vaccination of subjects aged 11 to 17 years with the quadrivalent meningococcal vaccine conjugated to tetanus toxoid (MenACWY-TT) or the quadrivalent meningococcal polysaccharide vaccine (MenACWY-PS). This extension study evaluated the safety and immunogenicity of a MenACWY-TT booster 10 years after receiving a primary dose of either MenACWY-TT or MenACWY-PS. The primary immunogenicity endpoint was booster response, evaluated using serum bactericidal antibody assays with rabbit complement (rSBA), 1 month postbooster. Safety endpoints included the percentage of subjects experiencing local and general adverse events (AEs) ≤4 days after MenACWY-TT booster. Of 229 subjects enrolled, 169 and 58 in the MenACWY-TT and MenACWY-PS groups, respectively, completed the booster phase. The 1 month postbooster response for each serogroup ranged from 81.5% to 95.7% for MenACWY-TT and 66.7% to 94.1% for MenACWY-PS. Similar percentages of MenACWY-TT and MenACWY-PS recipients had a booster response to serogroups A, W, and Y, whereas more MenACWY-TT recipients than MenACWY-PS recipients had a booster response to serogroup C. For the MenACWY-TT and MenACWY-PS groups, respectively, the MenACWY-TT booster elicited rSBA titers ≥1:8 in 100% and ≥98.0% of subjects across all serogroups; 100% and ≥96.1% of all subjects had titers ≥1:128. No new safety signals were observed during the booster phase. In conclusion, a MenACWY-TT booster dose after receiving either a primary dose of MenACWY-TT or MenACWY-PS elicited robust immune responses and was well tolerated. Functional antibody responses last up to 10 years after primary MenACWY-TT vaccination.
先前的一项 3 期、随机、多中心研究表明,11 至 17 岁的受试者接受破伤风类毒素结合的四价脑膜炎球菌疫苗(MenACWY-TT)或四价脑膜炎球菌多糖疫苗(MenACWY-PS)的初级免疫接种后,其免疫原性。这项扩展研究评估了在接受 MenACWY-TT 或 MenACWY-PS 初级剂量后 10 年接受 MenACWY-TT 加强针的安全性和免疫原性。主要免疫原性终点是加强针后 1 个月使用兔补体血清杀菌抗体测定(rSBA)评估的加强针反应。安全性终点包括 MenACWY-TT 加强针后≤4 天经历局部和全身不良事件(AE)的受试者比例。在 229 名入组的受试者中,169 名和 58 名分别在 MenACWY-TT 和 MenACWY-PS 组完成了加强针阶段。加强针后 1 个月,每个血清型组的反应率范围为 MenACWY-TT 为 81.5%至 95.7%,MenACWY-PS 为 66.7%至 94.1%。接受 MenACWY-TT 和 MenACWY-PS 的受试者中,有类似比例的受试者对血清型 A、W 和 Y 产生了加强针反应,而接受 MenACWY-TT 的受试者比接受 MenACWY-PS 的受试者对血清型 C 产生了更多的加强针反应。对于 MenACWY-TT 和 MenACWY-PS 组,MenACWY-TT 加强针在所有血清型组中分别引起 100%和≥98.0%的受试者 rSBA 滴度≥1:8;所有受试者中有 100%和≥96.1%的受试者的滴度≥1:128。在加强针阶段未观察到新的安全性信号。总之,在接受 MenACWY-TT 或 MenACWY-PS 初级剂量后接种 MenACWY-TT 加强针可引起强烈的免疫反应,并具有良好的耐受性。初级 MenACWY-TT 接种后,功能性抗体反应可持续长达 10 年。