Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, United States.
Programa de Pós-graduação em Medicina Veterinária, Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
Front Immunol. 2024 Feb 28;15:1322879. doi: 10.3389/fimmu.2024.1322879. eCollection 2024.
Orf virus (ORFV) is a large DNA virus that can harbor and efficiently deliver viral antigens in swine. Here we used ORFV as a vector platform to deliver chimeric hemagglutinins (HA) of Influenza A virus of swine (IAV-S). Vaccine development against IAV-S faces limitations posed by strain-specific immunity and the antigenic diversity of the IAV-S strains circulating in the field. A promising alternative aiming at re-directing immune responses on conserved epitopes of the stalk segment of the hemagglutinin (HA2) has recently emerged. Sequential immunization with chimeric HAs comprising the same stalk but distinct exotic head domains can potentially induce cross-reactive immune responses against conserved epitopes of the HA2 while breaking the immunodominance of the head domain (HA1). Here, we generated two recombinant ORFVs expressing chimeric HAs encoding the stalk region of a contemporary H1N1 IAV-S strain and exotic heads derived from either H6 or H8 subtypes, ORFVcH6/1 and ORFVcH8/1, respectively. The resulting recombinant viruses were able to express the heterologous protein . Further, the immunogenicity and cross-protection of these vaccine candidates were assessed in swine after sequential intramuscular immunization with OV-cH6/1 and OV-cH8/1, and subsequent challenge with divergent IAV-S strains. Humoral responses showed that vaccinated piglets presented increasing IgG responses in sera. Additionally, cross-reactive IgG and IgA antibody responses elicited by immunization were detected in sera and bronchoalveolar lavage (BAL), respectively, by ELISA against different viral clades and a diverse range of contemporary H1N1 IAV-S strains, indicating induction of humoral and mucosal immunity in vaccinated animals. Importantly, viral shedding was reduced in nasal swabs from vaccinated piglets after intranasal challenge with either Oh07 (gamma clade) or Ca09 (npdm clade) IAV-S strains. These results demonstrated the efficiency of ORFV-based vectors in delivering chimeric IAV-S HA-based vaccine candidates and underline the potential use of chimeric-HAs for prevention and control of influenza in swine.
口疮病毒(ORFV)是一种大型 DNA 病毒,能够在猪体内有效携带和传递病毒抗原。在这里,我们使用 ORFV 作为载体平台,传递猪流感病毒(IAV-S)的嵌合血凝素(HA)。针对 IAV-S 的疫苗开发面临着由菌株特异性免疫和田间流行的 IAV-S 菌株的抗原多样性带来的限制。最近出现了一种有前途的替代方法,旨在将免疫反应重新定向到血凝素(HA)茎段的保守表位上。通过连续免疫包含相同茎但具有不同外来头部结构域的嵌合 HAs,有可能诱导针对 HA2 的保守表位的交叉反应性免疫反应,同时打破头部结构域(HA1)的免疫优势。在这里,我们生成了两种表达嵌合 HAs 的重组 ORFV,这些 HAs 编码了当代 H1N1 IAV-S 菌株的茎区和源自 H6 或 H8 亚型的外来头部,分别命名为 ORFVcH6/1 和 ORFVcH8/1。所得重组病毒能够表达异源蛋白。此外,通过顺序肌肉内免疫 OV-cH6/1 和 OV-cH8/1,然后用不同的 IAV-S 菌株进行攻毒,评估了这些候选疫苗在猪中的免疫原性和交叉保护作用。体液反应表明,接种仔猪的血清 IgG 反应逐渐增加。此外,通过 ELISA 针对不同的病毒分支和一系列当代 H1N1 IAV-S 菌株,在血清和支气管肺泡灌洗液(BAL)中检测到免疫接种诱导的交叉反应性 IgG 和 IgA 抗体反应,表明接种动物诱导了体液和黏膜免疫。重要的是,在接种仔猪经鼻腔攻毒后,鼻腔拭子中的病毒脱落减少,攻毒用的病毒株分别为 Oh07(γ 分支)和 Ca09(npdm 分支)IAV-S 菌株。这些结果证明了基于 ORFV 的载体在传递基于嵌合 IAV-S HA 的疫苗候选物方面的效率,并强调了嵌合-HA 用于预防和控制猪流感的潜力。