Transcutaneous Immunization with a Band-Aid Prevents Experimental Otitis Media in a Polymicrobial Model.

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-06-05 Print Date: 2017-06-01 DOI:10.1128/CVI.00563-16
Laura A Novotny, John D Clements, Steven D Goodman, Lauren O Bakaletz
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引用次数: 23

Abstract

Otitis media (OM) is a common pediatric disease, and nontypeable Haemophilus influenzae (NTHI) is the predominant pathogen in chronic OM, recurrent OM, and OM associated with treatment failure. OM is also a polymicrobial disease, wherein an upper respiratory tract viral infection predisposes to ascension of NTHI from the nasopharynx, the site of colonization, to the normally sterile middle ear, resulting in disease. Using a clinically relevant viral-bacterial coinfection model of NTHI-induced OM, we performed transcutaneous immunization (TCI) via a band-aid delivery system to administer each of three promising NTHI vaccine candidates derived from bacterial adhesive proteins and biofilm mediators: recombinant soluble PilA (rsPilA), chimV4, and integration host factor. Each immunogen was admixed with the adjuvant LT(R192G/L211A), a double mutant of Escherichia coli heat-labile enterotoxin, and assessed for relative ability to prevent the onset of experimental OM. For each cohort, the presence of circulating immunogen-specific antibody-secreting cells and serum antibody was confirmed prior to intranasal NTHI challenge. After bacterial challenge, blinded video otoscopy and tympanometry revealed a significant reduction in the proportion of animals with signs of OM compared to levels in animals receiving adjuvant only, with an overall vaccine efficacy of 64 to 77%. These data are the first to demonstrate the efficacy afforded by TCI with a band-aid vaccine delivery system in a clinically relevant polymicrobial model of OM. The simplicity of TCI with a band-aid and the significant efficacy observed here hold great promise for reducing the global burden of OM in the pediatric population.

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多微生物模型中经皮创可贴免疫可预防实验性中耳炎。
中耳炎(OM)是一种常见的儿科疾病,不可分型的流感嗜血杆菌(NTHI)是慢性OM、复发性OM和与治疗失败相关的OM的主要病原体。OM也是一种多微生物疾病,其中上呼吸道病毒感染易使NTHI从定植部位鼻咽部上升到通常无菌的中耳,从而导致疾病。利用临床相关的NTHI诱导OM的病毒-细菌共感染模型,我们通过创可贴递送系统进行了经皮免疫(TCI),分别接种三种有希望的NTHI候选疫苗,这些候选疫苗来自细菌粘附蛋白和生物膜介质:重组可溶性PilA (rsPilA)、chimV4和整合宿主因子。将每种免疫原与佐剂LT(R192G/L211A)(大肠杆菌热不稳定肠毒素的双突变体)混合,并评估其预防实验性OM发病的相对能力。对于每个队列,在鼻内NTHI攻击之前确认循环免疫原特异性抗体分泌细胞和血清抗体的存在。在细菌攻击后,盲法视频耳镜检查和鼓室测量显示,与仅接受佐剂的动物相比,出现OM症状的动物比例显著降低,总体疫苗效力为64%至77%。这些数据首次在临床相关的多发性骨髓瘤多微生物模型中证明了TCI与创可贴疫苗递送系统的有效性。使用创可贴的TCI的简单性和在此观察到的显著疗效为减轻儿科人口OM的全球负担带来了巨大的希望。
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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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