摘要
旨在构建一种由山羊支原体山羊肺炎亚种(Mycoplasma capricolum Subsp.capripneumoniae,Mccp)六个B细胞表位和三个T细胞表位组成的多重抗原肽(multiple antigenic peptide,MAP),将其在大肠杆菌中表达后免疫小鼠,评估其体液免疫和细胞免疫。分别用MAP、单个B细胞表位及全菌超破抗原作为抗原,检测免疫小鼠抗体水平,结果显示三种抗原均能和小鼠免疫血清发生很好的反应(P<0.01)。体外代谢抑制试验显示,1∶64倍稀释的免疫小鼠血清可以有效抑制Mccp的生长。淋巴细胞增殖试验显示,当用单个T细胞表位及Mccp超破抗原分别刺激免疫小鼠的淋巴细胞时均产生明显的增殖现象(P<0.01)。细胞因子检测结果显示,免疫小鼠的IFN-γ、TNF-α、IL-1β和IL-10产量明显升高(P<0.001),而IL-12产量明显下降(P<0.001)。数据显示,构建的MAP能够引起小鼠的免疫反应,这一结果为由Mccp引起的山羊传染性胸膜肺炎亚单位疫苗的研制奠定了一定的基础。
A multiple antigenic peptide （MAP）, composed of six B-ceil epitopes and three T-cell epitopes derived from antigenic proteins of Mycoplasma capricolum subsp, capripneumoniae （Mcep）, was designed and expressed in Escherichia coli cells, which was then injected into mice to evaluate humoral and cellular immune responses induced by the recombinant MAP. Antibody levels against MAP, each single B-cell epitope, and the ultrasonic-treated crude Mccp antigen were all significantly increased （P〈0.01）. Results of in vitro metabolic inhibition test indicated that diluted sera （1.64） from immunized mice inhibited Mccp growth. Splenic lymphocytes from the immunized mice exhibited remarkable proliferation when stimulated by each single T-cell epitope and crude Mccp antigen （P〈0.01）. The production of IFN-γ, TNF-α, IL-β, and IL-10 were increased （P〈0. 001）, while that of IL-12 was decreased （P〈0. 001）. These data showed that the constructed MAP stimulated immune responses in mice. The results laid a certain foundation to develop subunit vaccine against contagious caprine pleuropneumonia caused by Mccp.
出处
《畜牧兽医学报》
CAS
CSCD
北大核心
2016年第12期2476-2482,共7页
ACTA VETERINARIA ET ZOOTECHNICA SINICA
基金
国家科技支撑计划(2015BAD12B02)
十三五项目"牛羊重要病原体分子检测新技术研究"(2016YFD0500907)
关键词
免疫反应
小鼠
多重抗原肽
山羊支原体山羊肺炎亚种
immune response
mice
multiple antigenic peptides
Mycoplasma capricolum subsp.capripneumoniae
