Immunogenicity and Safety of a Quadrivalent Meningococcal Conjugate Vaccine (MenACYW-TT) Administered with Routine Pediatric Vaccines: A European Randomized Controlled Trial.

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES
Federico Martinon-Torres, Miia M Virta, Susanna Koski, Ignacio Salamanca de la Cueva, Henryk T Szymanski, Samantha Bosis, Anca C Drăgănescu, Sven-Arne Silfverdal, Betzana Zambrano, Mandeep S Dhingra, Siham B'Chir, Olga Syrkina, Olga Lyabis, Gustavo A Vasquez, Christine Rehm
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引用次数: 0

Abstract

Introduction: The immunogenicity and safety of MenACYW-TT (MenQuadfi®) were compared to another quadrivalent meningococcal conjugate vaccine, MCV4-TT (Nimenrix®), when administered in infants alongside routine childhood vaccines in Europe.

Methods: One set of healthy infants was randomized 1:1 to receive MenACYW-TT (group 1; n = 714) or MCV4-TT (group 2; n = 726) at age 2, 4, and 12-18 months (2 + 1 regimen) concomitantly with routine vaccines (including 10-valent pneumococcal conjugate vaccine). Another set was randomized 1:1 to receive MenACYW-TT in a 2 + 1 regimen (group 3; n = 112) or a 3 + 1 regimen at age 2, 4, 6, and 12-18 months (group 4; n = 108) concomitantly with routine vaccines (including 13-valent pneumococcal conjugate vaccine). Immune responses against meningococcal serogroups A, C, W, and Y were measured by serum bactericidal assay using human complement (hSBA). Non-inferiority of MenACYW-TT versus MCV4-TT was based on hSBA geometric mean titers (GMTs) 30 days post-booster (dose 3; primary endpoint) and rates of seroprotection 30 days post-dose 2 (secondary endpoint) against all vaccine meningococcal serogroups. Immune responses to co-administered vaccines and safety were also assessed. Post hoc, non-inferiority of MenACYW-TT was also assessed based on seroresponse rates 30 days post-booster.

Results: Non-inferiority of MenACYW-TT versus MCV4-TT, based on GMTs post-booster, was demonstrated for serogroups C, W, and Y but not for A. GMTs against serogroups C, W, and Y were 1.5- to 4.5-fold higher with MenACYW-TT than MCV4-TT; those against serogroup A were marginally lower. Antibody responses in groups 3 and 4 against all serogroups were similar to group 1. Non-inferiority of MenACYW-TT based on seroresponse rates post-booster against all serogroups was demonstrated post hoc. No interference with concomitant routine vaccines nor safety concerns were identified.

Conclusions: Consideration of all immunogenicity and safety data generated in this study supports the incorporation of MenACYW-TT into the routine childhood vaccination schedule as a 2 + 1 regimen starting at age 6 weeks.

Clinicaltrials:

Gov identifier: NCT03547271.

四价脑膜炎球菌结合疫苗(MenACYW-TT)与常规儿科疫苗的免疫原性和安全性:一项欧洲随机对照试验
研究人员将MenACYW-TT (MenQuadfi®)的免疫原性和安全性与另一种四价脑膜炎球菌结合疫苗MCV4-TT (Nimenrix®)进行了比较,后者在欧洲与常规儿童疫苗一起用于婴儿。方法:1组健康婴儿按1:1随机接受MenACYW-TT治疗(1组;n = 714)或MCV4-TT(2组;N = 726),分别为2、4和12-18个月(2 + 1方案),同时接种常规疫苗(包括10价肺炎球菌结合疫苗)。另一组以1:1的比例随机分配,以2 + 1方案接受MenACYW-TT治疗(第3组;N = 112)或在2、4、6和12-18个月时采用3 + 1方案(第4组;N = 108)与常规疫苗(包括13价肺炎球菌结合疫苗)同时接种。采用人补体(hSBA)血清杀菌法测定对脑膜炎球菌血清A、C、W和Y群的免疫应答。MenACYW-TT与MCV4-TT的非劣效性是基于增强后30天(剂量3;(主要终点)和第2剂后30天(次要终点)对所有脑膜炎球菌疫苗血清群的血清保护率。还评估了对联合接种疫苗的免疫反应和安全性。事后,MenACYW-TT的非劣效性也根据增强后30天的血清反应率进行评估。结果:基于增强后的GMTs, MenACYW-TT与MCV4-TT的非劣效性被证明适用于C、W和Y血清组,但不适用于a血清组。MenACYW-TT对C、W和Y血清组的GMTs比MCV4-TT高1.5- 4.5倍;血清A组的患者则略低。3、4组对各血清组的抗体反应与1组相似。基于增强后对所有血清组的血清反应率,事后证明了MenACYW-TT的非劣效性。未发现对伴随常规疫苗的干扰,也未发现安全问题。结论:考虑到本研究中产生的所有免疫原性和安全性数据,支持将MenACYW-TT作为从6周龄开始的2 + 1方案纳入常规儿童疫苗接种计划。临床试验:政府标识符:NCT03547271。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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