Podcast: Immune Persistence After Primary Vaccination with MenQuadfi.

IF 5.6 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2026-08-01 Epub Date: 2026-06-08 DOI:10.1007/s40121-026-01370-z
Mika Rämet, Mike Simon
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引用次数: 0

Abstract

Invasive meningococcal disease (IMD) remains a serious global health concern. Although incidence is generally low, the disease progresses rapidly and carries high fatality rates of 10-15%, with survivors often experiencing long-term sequelae including hearing loss, neurological impairment, or limb amputations. These consequences highlight the need for effective and durable vaccination strategies. IMD incidence and serogroup distribution vary geographically. The highest burden occurs in the African meningitis belt, historically dominated by serogroup A, though recent outbreaks have increasingly involved serogroups C, W, and X. In Europe, serogroup B is most common, particularly in infants and adolescents, while serogroup Y is rising among adults aged ≥ 65 years. These geographical and demographic differences underscore the importance of region-specific vaccination policies. Polysaccharide vaccines targeting serogroups A, C, W, and Y have played an essential role in outbreak control but are associated with certain limitations: they do not induce immune memory and are poorly immunogenic in infants. These limitations led to the development of conjugate vaccines, where polysaccharide antigens are linked to protein carriers to enhance immunogenicity and memory responses. Several quadrivalent conjugate vaccines (MenACWY), MenQuadfi®, Menveo®, and Nimenrix®, are available, which target the same four serogroups, but differ in antigen composition and carrier proteins. However, access to meningococcal vaccines varies across regions. In this podcast, Professor Mika Rämet and Dr Mike Simon discuss the concept of immune persistence and its relevance for evaluating long-term protection provided by quadrivalent meningococcal vaccines. They review persistence data for MenQuadfi from recent clinical trials and a modeling study across multiple age groups and timepoints, comparing these findings with persistence data for other quadrivalent vaccines. Overall, the evidence supports the use of MenQuadfi as a MenACWY option, including for children, to help provide and maintain protection against IMD in the years following primary vaccination.Podcast available for this article. Supplementary material 1 (MP2 156850 kb).

播客:初次接种MenQuadfi后的免疫持久性。
侵袭性脑膜炎球菌病(IMD)仍然是一个严重的全球卫生问题。虽然发病率一般较低,但该病进展迅速,死亡率高达10-15%,幸存者通常会出现长期后遗症,包括听力丧失、神经损伤或肢体截肢。这些后果突出表明需要有效和持久的疫苗接种战略。IMD发病率和血清组分布在地理上有所不同。最高的负担发生在非洲脑膜炎带,历史上以血清组A为主,尽管最近的疫情越来越多地涉及血清组C、W和x。在欧洲,血清组B最常见,特别是在婴儿和青少年中,而血清组Y在年龄≥65岁的成年人中也在上升。这些地理和人口差异强调了针对特定区域的疫苗接种政策的重要性。针对血清群A、C、W和Y的多糖疫苗在疫情控制中发挥了重要作用,但存在某些局限性:它们不能诱导免疫记忆,在婴儿中免疫原性较差。这些限制导致了结合疫苗的发展,其中多糖抗原与蛋白质载体连接以增强免疫原性和记忆反应。几种四价结合疫苗(MenACWY), MenQuadfi®,Menveo®和Nimenrix®,可用于相同的四个血清群,但抗原组成和载体蛋白不同。然而,各区域获得脑膜炎球菌疫苗的情况各不相同。在本期播客中,米卡教授Rämet和迈克·西蒙博士讨论了免疫持久性的概念及其与评估四价脑膜炎球菌疫苗提供的长期保护的相关性。他们回顾了来自最近的临床试验和跨多个年龄组和时间点的建模研究的MenQuadfi的持久性数据,并将这些发现与其他四价疫苗的持久性数据进行了比较。总的来说,证据支持使用MenQuadfi作为MenACWY选项,包括儿童,以帮助在初次接种疫苗后的几年中提供和维持对IMD的保护。本文提供播客。补充资料1 (MP2 156850 kb)。
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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