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A、C、W、Y 群脑膜炎奈瑟球菌-破伤风类毒素结合疫苗加强免疫 10 年后的效力和安全性与破伤风类毒素结合疫苗或多糖疫苗的长期持久性

Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine.

机构信息

Clinical Research Division, Research Institute for Tropical Medicine , Alabang, Muntinlupa City, Philippines.

Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.

出版信息

Hum Vaccin Immunother. 2020 Jun 2;16(6):1272-1279. doi: 10.1080/21645515.2020.1744363. Epub 2020 May 13.

DOI:10.1080/21645515.2020.1744363
PMID:32401600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7482828/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/cd8151a0ef0f/KHVI_A_1744363_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/39652ad9e1c3/KHVI_A_1744363_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/1a03d6b2cea9/KHVI_A_1744363_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/cd8151a0ef0f/KHVI_A_1744363_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/39652ad9e1c3/KHVI_A_1744363_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/1a03d6b2cea9/KHVI_A_1744363_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/7482828/cd8151a0ef0f/KHVI_A_1744363_F0003_C.jpg

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