CpG寡核苷酸
产肠毒素大肠杆菌
生物
先天免疫系统
免疫学
CpG站点
免疫
抗原
被动免疫
抗体
鼻腔给药
免疫系统
多克隆抗体
微生物学
肠毒素
大肠杆菌
基因
基因表达
DNA甲基化
生物化学
作者
Haiming Cai,Zheshi Kuang,Kuiying Huang,Juqing Shi,Xiangjie Zhao,Pingping Chu,Chao‐Yuan Huang,Feiping Ming,Fenggeng Xia,Jun Yang,Linghua Zhang
标识
DOI:10.1016/j.vetimm.2014.07.003
摘要
CpG motifs activates mammalian lymphocytes and macrophages to produce cytokines and polyclonal Ig. These include IFN-γ, IL-12, TNF-a, which are important in the control of bacterial infection. But thus far, the innate immunostimulatory effects of CpG ODN against pathogen have been established mainly in mouse, monkey, sheep, chicken, but not in neonatal piglets. The purpose of this study is to determine the potential protection of CpG ODN against enterotoxigenic Escherichia coli (ETEC) (with which neonatal piglets were susceptible to infection in our lab) in neonatal piglets. Here, we show intranasal (IN)—mucosal and intramuscularly (IM) systemic administration of CpG ODN could enhance innate cellular (cytokine) immunity in the sera and intestine mucosa post challenge, and thereafter the development of antigen-specific antibodies in piglets. IN and IM immunizations of neonatal piglets without antigen both reduced the ETEC excretion and alleviated diarrhoea symptoms upon challenge, and IN route had better protection effects than IM route. Protection in this study was linked to induction of a Th1 response which induced by CpG ODN. Co-delivery with Emulsigen (EM), could improve protection mediated by CpG ODN. These observations indicate that IN administration of 100 μg/kg CpG ODN with 20% EM codelivery may represent a valuable strategy for induction of innate immunity against ETEC infection in neonatal piglets.
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