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An Alphavirus Replicon-Based Human Metapneumovirus Vaccine Is Immunogenic and Protective in Mice and Cotton Rats▿

机译:基于甲病毒复制子的人类偏肺病毒疫苗在小鼠和棉鼠中具有免疫原性和保护性。

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摘要

Human metapneumovirus (hMPV) is a recently discovered paramyxovirus that causes upper and lower respiratory tract infections in infants, the elderly, and immunocompromised individuals worldwide. Here, we developed Venezuelan equine encephalitis virus replicon particles (VRPs) encoding hMPV fusion (F) or attachment (G) glycoproteins and evaluated the immunogenicity and protective efficacy of these vaccine candidates in mice and cotton rats. VRPs encoding hMPV F protein, when administered intranasally, induced F-specific virus-neutralizing antibodies in serum and immunoglobulin A (IgA) antibodies in secretions at the respiratory mucosa. Challenge virus replication was reduced significantly in both the upper and lower respiratory tracts following intranasal hMPV challenge in these animals. However, vaccination with hMPV G protein VRPs did not induce neutralizing antibodies or protect animals from hMPV challenge. Close examination of the histopathology of the lungs of VRP-MPV F-vaccinated animals following hMPV challenge revealed no enhancement of inflammation or mucus production. Aberrant cytokine gene expression was not detected in these animals. Together, these results represent an important first step toward the use of VRPs encoding hMPV F proteins as a prophylactic vaccine for hMPV.
机译:人类偏肺病毒(hMPV)是最近发现的副粘病毒,可引起全球婴儿,老年人和免疫功能低下者的上呼吸道和下呼吸道感染。在这里,我们开发了编码hMPV融合(F)或附着(G)糖蛋白的委内瑞拉马脑炎病毒复制子颗粒(VRP),并评估了这些候选疫苗在小鼠和棉鼠中的免疫原性和保护功效。鼻内给药时,编码hMPV F蛋白的VRP诱导血清中F特异性病毒中和抗体和呼吸道粘膜分泌物中的免疫球蛋白A(IgA)抗体。在这些动物中,鼻内hMPV攻击后,挑战病毒的复制在上呼吸道和下呼吸道均显着降低。但是,用hMPV G蛋白VRP接种疫苗不会诱导中和抗体或保护动物免受hMPV攻击。 hMPV攻击后,对VRP-MPV F疫苗接种动物的肺组织病理学进行了仔细检查,结果显示炎症或粘液产生没有增强。在这些动物中未检测到异常的细胞因子基因表达。总之,这些结果代表了使用编码hMPV F蛋白的VRP作为hMPV预防疫苗的重要的第一步。

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