UR892 INRA, 78350 Jouy-en-Josas, France.
Vaccine. 2010 May 7;28(21):3722-34. doi: 10.1016/j.vaccine.2010.03.008. Epub 2010 Mar 20.
Human and bovine respiratory syncytial viruses (HRSV and BRSV) are two closely related, worldwide prevalent viruses that are the leading cause of severe airway disease in children and calves, respectively. Efficacy of commercial bovine vaccines needs improvement and no human vaccine is licensed yet. We reported that nasal vaccination with the HRSV nucleoprotein produced as recombinant ring-shaped nanoparticles (N(SRS)) protects mice against a viral challenge with HRSV. The aim of this work was to evaluate this new vaccine that uses a conserved viral antigen, in calves, natural hosts for BRSV. Calves, free of colostral or natural anti-BRSV antibodies, were vaccinated with N(SRS) either intramuscularly, or both intramuscularly and intranasally using Montanide ISA71 and IMS4132 as adjuvants and challenged with BRSV. All vaccinated calves developed anti-N antibodies in blood and nasal secretions and N-specific cellular immunity in local lymph nodes. Clinical monitoring post-challenge demonstrated moderate respiratory pathology with local lung tissue consolidations for the non-vaccinated calves that were significantly reduced in the vaccinated calves. Vaccinated calves had lower viral loads than the non-vaccinated control calves. Thus N(SRS) vaccination in calves provided cross-protective immunity against BRSV infection without adverse inflammatory reaction.
人呼吸道合胞病毒(HRSV)和牛呼吸道合胞病毒(BRSV)是两种密切相关的、全球流行的病毒,分别是导致儿童和牛严重呼吸道疾病的主要原因。商业牛用疫苗的效果需要改进,而且目前还没有获得许可的人用疫苗。我们曾报道,鼻腔接种作为重组环形纳米颗粒(N(SRS))的 HRSV 核蛋白可保护小鼠免受 HRSV 病毒攻击。本工作旨在评估这种使用保守病毒抗原的新型疫苗,该抗原是 BRSV 的天然宿主牛的抗原。无初乳或天然抗 BRSV 抗体的小牛,用 Montanide ISA71 和 IMS4132 作为佐剂,通过肌肉内或肌肉内和鼻内接种 N(SRS),并用 BRSV 进行攻毒。所有接种疫苗的小牛均在血液和鼻分泌物中产生抗-N 抗体,在局部淋巴结中产生 N 特异性细胞免疫。攻毒后的临床监测表明,未接种疫苗的小牛出现中度呼吸道病理,肺部局部组织实变,而接种疫苗的小牛肺部组织实变明显减少。接种疫苗的小牛的病毒载量低于未接种疫苗的对照小牛。因此,在小牛中接种 N(SRS)可提供针对 BRSV 感染的交叉保护免疫,而无炎症反应。