鼠疫耶尔森菌
脂质体
抗原
双肌酸测定
免疫系统
抗体效价
效价
免疫
免疫
抗体
鼠疫(疾病)
微生物学
生物
免疫学
医学
生物化学
毒力
基因
病理
作者
Yuan‐Chuan Chen,Shiu‐Jau Chen,Hwei‐Fang Cheng,Ming‐Kung Yeh
标识
DOI:10.1016/j.jddst.2019.101443
摘要
The F1 protein of Yersinia pestis is a major antigen for triggering immunity against plague in animals. It was currently used as a model antigen to establish a technology platform for highly efficient antibody induction. F1 antigen-loaded liposomes (F1-liposomes) were prepared using the patent formulation of the platform. The F1-liposome was further tested in vitro using phosphate-buffered saline (PBS) as solvent and its F1 protein content was determined by bicinchoninic acid (BCA) assay. The prepared F1-liposomes were administered into immunocompetent Balb/c mice using microneedles to have them immunized. The blood of these immunized mice was periodically taken out every 7 days for 45 days for the evaluation of the anti-F1 IgG titer using enzyme-linked immunosorbent assay (ELISA). Furthermore, to confirm the immune responses, the contents of interleukin-4 (IL-4), interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) were determined 35 days post immunization using the BIO-Plex pro assay. The mice administered with F1-liposome demonstrated the strongest immunity by the anti-F1 IgG antibody titer assay, the cytokine response test and the animal challenge test, compare with the controls (PBS and F1-Alugel). These results show that it is possible to develop an effective F1-liposomes plague vaccine using microneedles as a delivery tool.
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