病毒学
免疫系统
免疫学
中和抗体
抗体
免疫
体液免疫
生物
医学
作者
Xin Miao,Liping Zhang,Peng Zhou,Ruiming Yu,Zhongwang Zhang,Cancan Wang,Huichen Guo,Yonglu Wang,Pan Li,Xinsheng Liu
出处
期刊:Vaccine
[Elsevier BV]
日期:2023-09-29
卷期号:41 (45): 6661-6671
被引量:2
标识
DOI:10.1016/j.vaccine.2023.09.053
摘要
Porcine deltacoronavirus (PDCoV) is a novel swine enteropathogenic coronavirus that causes severe watery diarrhea, vomiting, dehydration and high mortality in piglets, resulting in significant economic losses by the global pig industry. Recently, PDCoV has also shown the potential for cross-species transmission. However, there are currently few vaccine studies and no commercially available vaccines for PDCoV. Hence, here, two novel human adenovirus 5 (Ad5)-vectored vaccines expressing codon-optimized forms of the PDCoV spike (S) glycoprotein (Ad-PD-tPA-Sopt) and S1 glycoprotein (Ad-PD-oriSIP-S1opt) were constructed, and their effects were evaluated via intramuscular (IM) injection in BALB/c mice with different doses and times. Both vaccines elicited robust humoral and cellular immune responses; moreover, Ad-PD-tPA-Sopt-vaccinated mice after two IM injections with 108 infectious units (IFU)/mouse had significantly higher anti-PDCoV-specific neutralizing antibody titers. In contrast, the mice immunized with Ad-PD-tPA-Sopt via oral gavage (OG) did not generate robust systemic and mucosal immunity. Thus, IM Ad-PD-tPA-Sopt administration is a promising strategy against PDCoV and provides useful information for future animal vaccine development.
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