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Skin Vaccination against Rotavirus Using Microneedles: Proof of Concept in Gnotobiotic Piglets

机译:使用微针针对轮状病毒进行皮肤疫苗接种:生殖生物仔猪的概念证明

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摘要

Live-attenuated oral rotavirus (RV) vaccines have lower efficacy in low income countries, and additionally are associated with a rare but severe adverse event, intussusception. We have been pursuing the development of an inactivated rotavirus vaccine (IRV) using the human rotavirus strain CDC-9 (G1P[]) through parenteral immunization and previously demonstrated dose sparing and enhanced immunogenicity of intradermal (ID) unadjuvanted IRV using a coated microneedle patch in comparison with intramuscular (IM) administration in mice. The aim of this study was to evaluate the immune response and protection against RV infection and diarrhea conferred by the administration of the ID unadjuvanted IRV using the microneedle device MicronJet600® in neonatal gnotobiotic (Gn) piglets challenged with virulent Wa G1P[] human RV. Three doses of 5 μg IRV when administered intradermally and 5 μg IRV formulated with aluminum hydroxide [Al(OH)3] when administered intramuscularly induced comparable rotavirus-specific antibody titers of IgA, IgG, IgG avidity index and neutralizing activity in sera of neonatal piglets. Both IRV vaccination regimens protected against RV antigen shedding in stools, and reduced the cumulative diarrhea scores in the piglets. This study demonstrated that the ID and IM administrations of IRV are immunogenic and protective against RV-induced diarrhea in neonatal piglets. Our findings highlight the potential value of an adjuvant sparing effect of the IRV ID delivery route.
机译:减毒的口服轮状病毒(RV)疫苗在低收入国家的功效较低,并且还与罕见但严重的不良事件肠套叠有关。我们一直在通过肠胃外免疫使用人类轮状病毒CDC-9(G1P [])来开发灭活的轮状病毒疫苗(IRV),并且先前已证明了使用包衣的微针贴片可节省剂量并增强皮内(ID)无佐剂IRV的免疫原性与小鼠肌肉注射(IM)相比。这项研究的目的是评估使用微针设备MicronJet600 ®施用ID无佐剂的IRV给予有毒力的新生仔猪(Gn)仔猪的免疫应答以及对RV感染和腹泻的保护作用Wa G1P []人类RV。皮内注射时三剂5μgIRV,肌肉注射时用氢氧化铝[Al(OH)3]配制的5μgIRV诱导新生仔猪血清中IgA,IgG,IgG亲和力指数和中和活性相当的轮状病毒特异性抗体滴度。两种IRV疫苗接种方案均能防止粪便中RV抗原脱落,并降低了仔猪的累积腹泻评分。这项研究表明,IRV的ID和IM给药具有免疫原性,并能防止RV引起的仔猪腹泻。我们的发现突出了IRV ID传递途径的佐剂保护作用的潜在价值。

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