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不同佐剂的猪德尔塔冠状病毒灭活疫苗在小鼠中的研发与免疫原性评价。

Development and immunogenicity evaluation of porcine deltacoronavirus inactivated vaccine with different adjuvants in mice.

机构信息

International Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450046, China.

International Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450046, China.

出版信息

Vaccine. 2022 Jul 29;40(31):4211-4219. doi: 10.1016/j.vaccine.2022.05.085. Epub 2022 Jun 9.

Abstract

Porcine deltacoronavirus (PDCoV) is a novel coronavirus that causes diarrhea in pigs of various ages, especially in suckling piglets, and there are no effective measures to prevent and control PDCoV currently. In this study, two adjuvants Al(OH) and ODN2395 working through different mechanisms were used to prepare inactivated PDCoV vaccines, and the immune effects of PDCoV inactivated vaccines were assessed in mice. From the results, we found that both PDCoV/Al(OH) vaccine and PDCoV/2395 vaccine could induce IgG and neutralizing antibodies with high levels in mice. At the same time, cytokines of IFN-γ, IL-4 and chemokine ligand of CXCL13 in serum were significantly increased after immunization, and reached the highest levels in PDCoV/2395 vaccine group, which suggested that PDCoV/2395 could promote the production of both Th1 and Th2 polarized cytokines. In addition, histopathological observations showed that vaccination helped mice resist PDCoV infection. These results indicated that both the two inactivated vaccines have good immune effects. Moreover, the PDCoV/2395 vaccine worked better than the PDCoV/Al(OH) vaccine for PDCoV/2395 having the good ability to induce both humoral and cellular immunogenicity. The PDCoV/2395 inactivated vaccine developed in this study might be an effective tool for the prevention of PDCoV infection.

摘要

猪德尔塔冠状病毒(PDCoV)是一种新型冠状病毒,可引起各种年龄猪只,尤其是哺乳仔猪腹泻,目前尚无有效的预防和控制 PDCoV 的措施。本研究使用两种通过不同机制起作用的佐剂 Al(OH) 和 ODN2395 来制备 PDCoV 灭活疫苗,并在小鼠中评估 PDCoV 灭活疫苗的免疫效果。结果发现,PDCoV/Al(OH) 疫苗和 PDCoV/2395 疫苗均可诱导小鼠产生高水平的 IgG 和中和抗体。同时,免疫后血清中 IFN-γ、IL-4 细胞因子和趋化因子配体 CXCL13 显著增加,在 PDCoV/2395 疫苗组中达到最高水平,提示 PDCoV/2395 可促进 Th1 和 Th2 极化细胞因子的产生。此外,组织病理学观察表明,接种疫苗有助于小鼠抵抗 PDCoV 感染。这些结果表明,两种灭活疫苗均具有良好的免疫效果。而且,PDCoV/2395 疫苗比 PDCoV/Al(OH) 疫苗的效果更好,因为 PDCoV/2395 具有良好的诱导体液和细胞免疫原性的能力。本研究开发的 PDCoV/2395 灭活疫苗可能是预防 PDCoV 感染的有效工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e1d/9181634/83289ab97cd0/gr1_lrg.jpg

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