Echlin Haley, Iverson Amy, McKnight Abigail, Rosch Jason W
Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Vaccines (Basel). 2024 Dec 19;12(12):1432. doi: 10.3390/vaccines12121432.
: Acute otitis media (AOM) is a common pediatric infection worldwide and is the primary basis for pediatric primary care visits and antibiotic prescriptions in children. Current licensed vaccines have been incompletely ineffective at reducing the global burden of AOM, underscoring a major unmet medical need. The complex etiology of AOM presents additional challenges for vaccine development, as it can stem from multiple bacterial species including , , and . As such, targeting multiple pathogens simultaneously may be required to significantly impact the overall disease burden. : In this study, we aim to overcome this challenge by engineering a live-attenuated vaccine platform based on an attenuated mutant of that expresses and surface epitopes to induce protective immunity against all three pathogens. : The trivalent live-attenuated vaccine conferred significant protection against all three bacterial otopathogens as measured by seroconversion and the development of AOM, with the inclusion of the additional epitopes providing unexpected synergy and enhanced protection against . : These data demonstrate a novel mechanism of introducing non-native immunogenic antigens into a live-attenuated vaccine platform to engender protection against AOM from multiple pathogenic species.
急性中耳炎(AOM)是全球常见的儿科感染性疾病,也是儿童进行初级保健就诊和开具抗生素处方的主要原因。目前已获许可的疫苗在减轻全球AOM负担方面效果并不完全理想,这凸显了一个尚未满足的重大医疗需求。AOM的病因复杂,给疫苗研发带来了额外挑战,因为它可能源于多种细菌,包括[具体细菌种类1]、[具体细菌种类2]和[具体细菌种类3]。因此,可能需要同时针对多种病原体,才能显著影响总体疾病负担。
在本研究中,我们旨在通过构建一种基于[减毒菌株名称]减毒突变体的减毒活疫苗平台来克服这一挑战,该突变体表达[抗原1]和[抗原2]表面表位,以诱导针对所有三种病原体的保护性免疫。
通过血清转化和AOM的发生情况来衡量,三价减毒活疫苗对所有三种细菌性耳病原体均具有显著保护作用,额外表位的加入提供了意想不到的协同作用,并增强了对[具体病原体3]的保护。
这些数据证明了一种将非天然免疫原性抗原引入减毒活疫苗平台以产生针对多种致病菌种引起的AOM的保护作用的新机制。