辉瑞五价menabcy脑膜炎球菌疫苗延长给药间隔的免疫原性和安全性:一项随机2b期研究的结果

IF 5.2 3区 医学 Q1 IMMUNOLOGY
Vaccines Pub Date : 2026-04-15 DOI:10.3390/vaccines14040352
Jake C Jones, Mary D Tipton, Lefteris Zolotas, Jason D Maguire, Kelly Belanger, Yanping Liu, Roger Maansson, Robert E O'Neill, Paul Balmer, Paula Peyrani, Johannes Beeslaar
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引用次数: 0

摘要

背景/目的:脑膜炎球菌病主要由血清A、B、C、W和Y引起。目前美国疫苗接种建议包括常规血清A/C/W/Y (MenACWY)疫苗接种(11-12岁和16岁)和基于共同临床决策的两剂、0- 6个月的MenB疫苗接种系列(16-23岁)。辉瑞五价MenABCWY疫苗(PenbrayaTM)于2023年获得美国许可,作为两剂,0- 6个月系列,当MenACWY和MenB疫苗被推荐在同一次就诊时被批准。本研究评估了两种延长的双剂量menabcy在健康青少年中的免疫原性和安全性。方法:在这项观察者盲法的2b期研究(ClinicalTrials.gov, NCT04440176; 2020年6月19日)中,309名11至14岁的健康儿童被1:1随机分组,接受0、36个月或0、12个月的辉瑞MenACWY疫苗接种计划,该计划与目前美国MenACWY疫苗接种建议更接近。终点包括使用人补体血清保护率(滴度≥1:8或≥1:16,取决于菌株)的血清杀菌试验,血清应答率(比基线滴度增加≥4倍)和几何平均滴度(GMTs)。安全性也进行了评估。结果:第二次辉瑞menabcy剂量1个月后,血清组A/B/C/W/Y的血清保护率在0- 36个月为100%,在0- 12个月为96.6-100%;血清有效率分别为100%和92.9-100%。在0个月和36个月的时间表中,gmt通常呈上升趋势。第二次接种0 ~ 12个月疫苗后24个月的血清保护率,B组为44.0 ~ 75.0%,A/C/W/Y组为88.9 ~ 100%。没有发现安全问题。结论:这些数据支持辉瑞menabcy在当前或未来可能的美国脑膜炎球菌疫苗接种框架中的剂量灵活性和实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenicity and Safety of Extended Dosing Intervals for Pfizer Pentavalent MenABCWY Meningococcal Vaccination in Healthy Adolescents: Results from a Randomized, Phase 2b Study.

Background/Objectives: Meningococcal disease is primarily caused by serogroups A, B, C, W, and Y. Current US vaccination recommendations include routine serogroup A/C/W/Y (MenACWY) vaccination (ages 11-12 and 16 years) and a two-dose, 0-, 6-month MenB vaccination series (age 16-23 years) based on shared clinical decision-making. Administration of the first-in-class Pfizer pentavalent MenABCWY vaccine (PenbrayaTM), which received US licensure in 2023 as a two-dose, 0-, 6-month series, is endorsed when the MenACWY and MenB vaccines are recommended at the same visit. This study evaluated the immunogenicity and safety of two extended two-dose schedules of MenABCWY in healthy adolescents. Methods: In this observer-blinded, phase 2b study (ClinicalTrials.gov, NCT04440176; 19 June 2020), 309 healthy 11- to 14-year-olds were randomized 1:1 to receive a 0-, 36-month or 0-, 12-month Pfizer MenABCWY schedule, which more closely aligns with current US MenACWY vaccination recommendations. Endpoints included serum bactericidal assay using human complement seroprotection rates (titers ≥ 1:8 or ≥1:16, depending on strain), seroresponse rates (≥4-fold increase from baseline titer), and geometric mean titers (GMTs). Safety was also assessed. Results: One month after the second Pfizer MenABCWY dose, serogroup A/B/C/W/Y seroprotection rates were 100% for the 0-, 36-month schedule and 96.6-100% for the 0-, 12-month schedule; seroresponse rates were 100% and 92.9-100%, respectively. GMTs generally trended higher with the 0-, 36-month schedule. Seroprotection rates through 24 months after the second dose of the 0-, 12-month schedule were 44.0-75.0% for serogroup B and 88.9-100% for serogroup A/C/W/Y). No safety issues were identified. Conclusions: These data support Pfizer MenABCWY dosing flexibility and utility within the current or possible future US meningococcal vaccination framework.

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来源期刊
Vaccines
Vaccines Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
8.90
自引率
16.70%
发文量
1853
审稿时长
18.06 days
期刊介绍: Vaccines (ISSN 2076-393X) is an international, peer-reviewed open access journal focused on laboratory and clinical vaccine research, utilization and immunization. Vaccines publishes high quality reviews, regular research papers, communications and case reports.
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