Zhang Cong, Zhou Jiangfei, Liu Zhixin, Liu Yongqing, Cai Kairui, Shen Tengfei, Liao Chengshui, Wang Chen
Key Laboratory of Veterinary Biological Engineering, Henan University of Science and Technology, Luoyang 471023, China.
J Vet Sci. 2018 Nov 30;19(6):817-826. doi: 10.4142/jvs.2018.19.6.817.
The bursa of Fabricius (BF) is a central humoral immune organ unique to birds. Four bursal peptides (BP-I, BP-II, BP-III, and BP-IV) have been isolated and identified from the BF. In this study, the immunoadjuvant activities of BPs I to IV were examined in mice immunized with H9N2 avian influenza virus (AIV) vaccine. The results suggested that BP-I effectively enhanced cell-mediated immune responses, increased the secretion of Th1 (interferon gamma)- and Th2 (interleukin-4)-type cytokines, and induced an improved cytotoxic T-lymphocyte (CTL) response to the H9N2 virus. BP-II mainly elevated specific antibody production, especially neutralizing antibodies, and increased Th1- and Th2-type cytokine secretion. BP-III had no significant effect on antibody production or cell-mediated immune responses compared to those in the control group. A strong immune response at both the humoral and cellular levels was induced by BP-IV. Furthermore, a virus challenge experiment followed by H&E staining revealed that BP-I and BP-II promoted removal of the virus and conferred protection in mouse lungs. BP-IV significantly reduced viral titers and histopathological changes and contributed to protection against H9N2 AIV challenge in mouse lungs. This study further elucidated the immunoadjuvant activities of BPs I to IV, providing a novel insight into immunoadjuvants for use in vaccine design.
法氏囊(BF)是鸟类特有的中枢体液免疫器官。已从法氏囊中分离并鉴定出四种法氏囊肽(BP-I、BP-II、BP-III和BP-IV)。在本研究中,检测了BP-I至BP-IV在接种H9N2禽流感病毒(AIV)疫苗的小鼠中的免疫佐剂活性。结果表明,BP-I有效增强细胞介导的免疫反应,增加Th1(干扰素γ)和Th2(白细胞介素-4)型细胞因子的分泌,并诱导对H9N2病毒的细胞毒性T淋巴细胞(CTL)反应增强。BP-II主要提高特异性抗体的产生,尤其是中和抗体,并增加Th1和Th2型细胞因子的分泌。与对照组相比,BP-III对抗体产生或细胞介导的免疫反应没有显著影响。BP-IV在体液和细胞水平均诱导了强烈的免疫反应。此外,病毒攻击实验及随后的苏木精-伊红染色显示,BP-I和BP-II促进了病毒的清除,并对小鼠肺部起到保护作用。BP-IV显著降低病毒滴度和组织病理学变化,并有助于保护小鼠肺部免受H9N2 AIV攻击。本研究进一步阐明了BP-I至BP-IV的免疫佐剂活性,为疫苗设计中免疫佐剂的使用提供了新的见解。