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免疫原性和安全性的四价脑膜炎球菌结合疫苗破伤风类毒素(MenACYW-TT)在脑膜炎球菌疫苗-初免参与者广泛的年龄范围(2-55 岁)在日本:一项 III 期随机研究。

Immunogenicity and Safety of a Quadrivalent Meningococcal Tetanus Toxoid-Conjugate Vaccine (MenACYW-TT) in Meningococcal Vaccine-Naïve Participants across a Broad Age Range (2-55 Years) in Japan: a Phase III Randomized Study.

机构信息

Medical Corporation Heishinkai ToCROM Clinic, Japan.

Disease Control and Prevention Center, National Center for Global Health and Medicine, Japan.

出版信息

Jpn J Infect Dis. 2023 May 24;76(3):174-182. doi: 10.7883/yoken.JJID.2022.272. Epub 2023 Jan 31.

Abstract

MenACYW-TT is a quadrivalent meningococcal tetanus toxoid-conjugate vaccine designed to prevent invasive meningococcal disease. The primary objective of this study was to demonstrate non-inferiority of the vaccine seroresponse to a single dose of MenACYW-TT compared with MCV4-DT, a licensed meningococcal quadrivalent diphtheria-conjugate vaccine. This Phase III double-blind, multicenter trial was conducted in meningococcal vaccine-naïve individuals aged 2-55 years in Japan (NCT04368429; jRCT2080225192). Participants were randomized 1:1 to receive either MenACYW-TT (n = 180) or MCV4-DT (n = 180). Functional antibodies against meningococcal serogroups A, C, W, and Y were measured using a serum bactericidal antibody assay with human complement (hSBA) at baseline (D0) and 30 days after vaccination (D30). Seroresponse was defined as a post-vaccination titer ≥1:16 in participants with a baseline titer <1:8; or a ≥4-fold increase in titer in participants with a baseline titer ≥1:8. Safety data were collected for 30 days. Non-inferiority of the seroresponse to MenACYW-TT vs. MCV4-DT was demonstrated on D30 for each serogroup tested (A: 85.6% vs. 65.4%; C: 96.6% vs. 62.6%; W: 87.4% vs. 49.2%; Y: 97.7% vs. 63.5%). MenACYW-TT was well tolerated with no safety concerns identified. A single dose of MenACYW-TT was well tolerated, with a non-inferior seroresponse compared with MCV4-DT. MenACYW-TT could thus be used as an alternative vaccine in meningococcal vaccine-naïve individuals.

摘要

MenACYW-TT 是一种四价脑膜炎奈瑟菌破伤风类毒素结合疫苗,旨在预防侵袭性脑膜炎奈瑟菌病。本研究的主要目的是证明与已上市的脑膜炎奈瑟菌四价二价结合疫苗 MCV4-DT 相比,MenACYW-TT 对单剂疫苗的血清反应具有非劣效性。这项 III 期、双盲、多中心试验在日本对脑膜炎奈瑟菌疫苗初免个体(2-55 岁)进行(NCT04368429;jRCT2080225192)。参与者按 1:1 随机分配至 MenACYW-TT 组(n=180)或 MCV4-DT 组(n=180)。在基线(D0)和接种后 30 天(D30),使用人补体血清杀菌抗体测定(hSBA)检测针对脑膜炎奈瑟菌血清群 A、C、W 和 Y 的功能性抗体。血清反应定义为接种后滴度≥1:16 的个体中,基线滴度<1:8;或基线滴度≥1:8 的个体中,滴度增加≥4 倍。在 30 天内收集安全性数据。在每个测试血清群中,MenACYW-TT 的血清反应均显示出非劣效性(A:85.6%vs.65.4%;C:96.6%vs.62.6%;W:87.4%vs.49.2%;Y:97.7%vs.63.5%)。MenACYW-TT 具有良好的耐受性,未发现安全性问题。MenACYW-TT 耐受性良好,与 MCV4-DT 相比,血清反应非劣效。因此,MenACYW-TT 可作为脑膜炎奈瑟菌疫苗初免个体的替代疫苗。

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