Presa Jessica, Findlow Jamie, Vojicic Jelena, Williams Scott, Serra Lidia
Global Medical Development and Scientific/Clinical Affairs, Pfizer Inc, Collegeville, PA, USA.
Medical and Scientific Affairs, International Developed Markets, Pfizer Ltd, Tadworth, Surrey, UK.
Infect Dis Ther. 2019 Sep;8(3):307-333. doi: 10.1007/s40121-019-0254-1. Epub 2019 Jul 25.
Neisseria meningitidis is a major cause of meningitis and septicemia with cases, outbreaks, and epidemics reported globally in industrialized and non-industrialized countries. N. meningitidis is categorized into 12 serogroups; however, only 5 serogroups (A, B, C, W, Y) are responsible for the majority of disease. Invasive meningococcal disease (IMD) occurs unpredictably; protection is therefore best achieved by initiating proactive vaccination strategies. Vaccines are currently available for the five main disease-causing serogroups. With the evolution of meningococcal vaccines and changes in IMD epidemiology, different vaccination strategies have been used. Recently, the rapid clonal expansion of meningococcal serogroup W (MenW) has been associated with a change in the national and regional vaccination recommendations from monovalent meningococcal serogroup C vaccines to meningococcal serogroup A, C, W, Y (MenACWY) vaccines in several countries. This review highlights these and other changes in IMD epidemiology and meningococcal vaccination recommendations, summarizes information available for currently available conjugate MenACWY vaccines, and focuses on clinical study data for the most recently approved MenACWY conjugate vaccine, MenACWY vaccine conjugated to tetanus toxoid (MenACWY-TT). MenACWY-TT studies spanned multiple age groups and generally demonstrated safety and immunogenicity in comparison with other meningococcal vaccines and under concomitant administration of other routine vaccines. Continuous updates to meningococcal vaccine recommendations in response to changing epidemiology, as have been undertaken for MenW, are necessary to ensure optimal population protection. FUNDING: Pfizer, Inc.
脑膜炎奈瑟菌是脑膜炎和败血症的主要病因,在工业化国家和非工业化国家均有全球范围内的病例、暴发和流行报告。脑膜炎奈瑟菌分为12个血清群;然而,只有5个血清群(A、B、C、W、Y)导致了大多数疾病。侵袭性脑膜炎球菌病(IMD)的发生不可预测;因此,通过启动主动疫苗接种策略可最佳地实现保护。目前有针对五个主要致病血清群的疫苗。随着脑膜炎球菌疫苗的演变和IMD流行病学的变化,已采用了不同的疫苗接种策略。最近,脑膜炎球菌血清群W(MenW)的快速克隆扩张与几个国家的国家和地区疫苗接种建议从单价脑膜炎球菌血清群C疫苗改为脑膜炎球菌血清群A、C、W、Y(MenACWY)疫苗有关。本综述强调了IMD流行病学和脑膜炎球菌疫苗接种建议的这些及其他变化,总结了现有结合型MenACWY疫苗的可用信息,并重点关注了最近批准的MenACWY结合疫苗——破伤风类毒素结合的MenACWY疫苗(MenACWY-TT)的临床研究数据。MenACWY-TT研究涵盖多个年龄组,与其他脑膜炎球菌疫苗相比,并在同时接种其他常规疫苗的情况下,总体显示出安全性和免疫原性。为确保最佳的人群保护,有必要根据流行病学变化持续更新脑膜炎球菌疫苗建议,就像针对MenW所做的那样。资助:辉瑞公司