病毒学
病毒
血凝试验
类病毒颗粒
小猎犬
鼻腔给药
效价
生物
免疫
甲型流感病毒
抗体
流感疫苗
医学
免疫学
基因
生物化学
重组DNA
遗传学
作者
Fei‐Fei Ge,Li-pin Shen,De-quan Yang,Xian-cao Yang,Xin Li,Haixiao Shen,Jian Wang,Shixin Huang
标识
DOI:10.1128/spectrum.00445-24
摘要
In 2016, a distinct branch of H3N2 canine influenza virus (CIV) emerged, which has mutations related to mammalian adaptation and has replaced previously prevalent strains. This branch poses a risk of zoonotic infection. To prevent and control H3N2 CIV, an H3N2 virus-like particle (VLP) vaccine based on the insect cell baculovirus expression system has been developed in the study. The H3N2 VLP vaccine induced high titers of hemagglutination inhibition (HI) antibodies in nasal and muscular immunized beagle dogs. Meanwhile, the VLP vaccine provided effective protection against homologous virus challenge comparable to inactivated H3N2 canine influenza virus. In addition, the intranasal H3N2 VLP vaccine induced significantly higher Th1, Th2, and Th17 immune responses, respectively (p,0.05). Importantly, intramuscular injection of VLP and inactivated H3N2 virus has complete protective effects against homologous H3N2 virus attacks. Nasal immunization with H3N2 VLP can partially protect beagles from H3N2 influenza.
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