在健康婴儿中,V114肺炎球菌疫苗与PCV13以2+1方案相比的安全性、耐受性和免疫原性:一项III期研究(PNEU-PED-EU-2)。

Safety, tolerability, and immunogenicity of V114 pneumococcal vaccine compared with PCV13 in a 2+1 regimen in healthy infants: A phase III study (PNEU-PED-EU-2).

作者信息

Benfield Thomas, Rämet Mika, Valentini Piero, Seppä Ilkka, Dagan Ron, Richmond Peter, Mercer Swati, Churchill Clay, Lupinacci Robert, McFetridge Richard, Park Jun, Wittke Frederick, Banniettis Natalie, Musey Luwy, Bickham Kara, Kaminski Janusz

机构信息

Department of Infectious Diseases, Copenhagen University Hospital, Hvidovre, Denmark.

Faculty of Medicine and Health Technology, Tampere University, and FVR - Finnish Vaccine Research, Tampere, Finland.

出版信息

Vaccine. 2023 Apr 6;41(15):2456-2465. doi: 10.1016/j.vaccine.2023.02.041. Epub 2023 Feb 24.

Abstract

BACKGROUND

This phase III study evaluated safety, tolerability, and immunogenicity of V114 (15-valent pneumococcal conjugate vaccine) in healthy infants. V114 contains all 13 serotypes in PCV13 and additional serotypes 22F and 33F.

METHODS

Healthy infants were randomized to two primary doses and one toddler dose (2+1 regimen) of V114 or PCV13 at 3, 5, and 12 months of age; diphtheria, tetanus, pertussis (DTaP), inactivated poliovirus (IPV), Haemophilus influenzae type b (Hib), hepatitis B (HepB) vaccine was administered concomitantly. Adverse events (AEs) were collected on Days 1-14 following each vaccination. Serotype-specific anti-pneumococcal immunoglobulin G (IgG) was measured 30 days post-primary series, immediately prior to toddler dose, and 30 days post-toddler dose. Primary objectives included non-inferiority of V114 to PCV13 for 13 shared serotypes and superiority of V114 to PCV13 for serotypes 22F and 33F.

RESULTS

1191 healthy infants were randomized to V114 (n = 595) or PCV13 (n = 596). Proportions of participants with solicited AEs and serious AEs were comparable between groups. V114 met non-inferiority criteria for 13 shared serotypes, based on difference in proportions with serotype-specific IgG ≥0.35 μg/mL (lower bound of two-sided 95% confidence interval [CI] >-10.0) and IgG geometric mean concentration (GMC) ratios (lower bound of two-sided 95% CI >0.5) at 30 days post-toddler dose. V114 met superiority criteria for serotypes 22F and 33F, based on response rates (lower bound of two-sided 95% CI >10.0) and IgG GMC ratios (lower bound of two-sided 95% CI >2.0) at 30 days post-toddler dose. Antibody responses to DTaP-IPV-Hib-HepB met non-inferiority criteria, based on antigen-specific response rates.

CONCLUSION

A two-dose primary series plus toddler dose of V114 was well-tolerated in healthy infants. Compared with PCV13, V114 provided non-inferior immune responses to 13 shared serotypes and superior immune responses to additional serotypes 22F and 33F.

摘要

背景

本III期研究评估了V114(15价肺炎球菌结合疫苗)在健康婴儿中的安全性、耐受性和免疫原性。V114包含13价肺炎球菌结合疫苗(PCV13)中的所有13种血清型以及另外的22F和33F血清型。

方法

健康婴儿在3、5和12月龄时被随机分为接受两剂基础剂量和一剂幼儿剂量(2+1方案)的V114或PCV13;同时接种白喉、破伤风、百日咳(DTaP)、灭活脊髓灰质炎病毒(IPV)、b型流感嗜血杆菌(Hib)、乙型肝炎(HepB)疫苗。在每次接种疫苗后的第1 - 14天收集不良事件(AE)。在基础免疫系列接种后30天、即将接种幼儿剂量前以及接种幼儿剂量后30天测量血清型特异性抗肺炎球菌免疫球蛋白G(IgG)。主要目标包括V114在13种共同血清型方面不劣于PCV13,以及V114在22F和33F血清型方面优于PCV13。

结果

1191名健康婴儿被随机分为V114组(n = 595)或PCV13组(n = 596)。两组中发生预期AE和严重AE的参与者比例相当。基于幼儿剂量接种后30天血清型特异性IgG≥0.35μg/mL的比例差异(双侧95%置信区间[CI]下限>-10.0)和IgG几何平均浓度(GMC)比值(双侧95% CI下限>0.5),V114满足13种共同血清型的非劣效标准。基于幼儿剂量接种后30天的反应率(双侧95% CI下限>10.0)和IgG GMC比值(双侧95% CI下限>2.0),V114满足22F和33F血清型的优效标准。基于抗原特异性反应率,对DTaP - IPV - Hib - HepB的抗体反应满足非劣效标准。

结论

在健康婴儿中,两剂基础系列加一剂幼儿剂量的V114耐受性良好。与PCV13相比,V114对13种共同血清型提供了非劣效的免疫反应,对另外的22F和33F血清型提供了优效的免疫反应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索