实验动物与比较医学 ›› 2018, Vol. 38 ›› Issue (2): 105-110.DOI: 10.3969/j.issn.1674-5817.2018.02.005

• 论著 • 上一篇    下一篇

壬二酸佐剂对甲型肝炎减毒活疫苗诱导小鼠体液免疫应答效应分析

李晓红1, 金晓1, 贾森泉2, 胡凝珠1, 胡云章1, 李建芳1   

  1. 1.中国医学科学院北京协和医学院医学生物学研究所云南省虫媒传染病防控研究重点实验室,昆明 650118;
    2.昆明医科大学,昆明 650500
  • 收稿日期:2017-11-28 出版日期:2018-04-25 发布日期:2018-04-25
  • 作者简介:李晓红(1991-),女,硕士研究生,专业:生物化学与分子生物学。E-mail:2579852980@qq.com
  • 基金资助:
    国家重点研发计划“高等级病原微生物实验室模拟培训体系研究”(2016YFC1202305);国家自然科学基金(31500724;31500748);云南省重大科技专项(2017ZF007);中国医学科学院医学与健康科学创新工程(2017-12M-3-022)

Effects of Azelaic Acid Adjuvant on Humoral Immune Response Induced by Hepatitis A Virus Attenuated Live Vaccine in Mice

LI Xiao-hong1, JIN Xiao1, JIA Sen-quan2, HU Ning-zhu1, HU Yun-zhan1, LI Jian-fang1   

  1. 1. Institute of Medical Biology,Chinese Academy of Medical Science and Peking Union Medical College,Yunnan Key Laboratory of Prevention & Control Research on Insect-borne Infectious Diseases,Kunming 650118,China;
    2. Kunming Medical University,Kunming 650500,China
  • Received:2017-11-28 Online:2018-04-25 Published:2018-04-25

摘要: 目的 探讨壬二酸作为佐剂对甲型肝炎减毒活疫苗(HepA-1)诱导小鼠体液免疫应答的影响, 以评价其佐剂效应。方法 分别将四种不同剂量的壬二酸(0.5 mg, 1 mg, 2 mg, 3 mg)与HepA-1共同免疫ICR小鼠分别作为佐剂组1、佐剂组2、佐剂组3、佐剂组4,同时设空白对照组、单纯抗原组、铝佐剂组,共免疫1次,于免疫后4周、8周、12周、16周进行尾静脉采血,采用间接酶联免疫吸附法(ELISA)检测小鼠血清抗甲型肝炎病毒(HAV) IgG抗体水平。结果 除空白对照组外,各组小鼠免疫后4周、8周、12周、16周,均产生抗HAV IgG抗体,抗体水平随免疫时间的延长逐渐升高,于8、12周达到峰值。免疫后4周,佐剂组4(壬二酸3 mg)产生的抗甲型肝炎病毒(HAV) IgG抗体水平与铝佐剂组相比较差异有统计学意义(P<0.05, t=2.640)。同时,佐剂组4在免疫后4周、8周和12周产生的抗甲型肝炎病毒(HAV) IgG抗体水平较高,显著高于单纯抗原组(P<0.05, t值分别为3.134、2.751、2.743)。结论 适当剂量的壬二酸可快速、显著提高HepA-1诱导小鼠的体液免疫应答,有望成为一种新型的人用疫苗佐剂。

关键词: 壬二酸, 疫苗佐剂, 甲型肝炎减毒活疫苗(HepA-1), 体液免疫

Abstract: Objective To investigate the effect of azelaic acid as an adjuvant on humoral immune response induced by hepatitis A virus (HAV) attenuated live vaccine (HepA-1) in mice to evaluate its adjuvant effect.Methods The ICR mice were injected respectively with HepA-1(18EU) and Al(OH)3(300 mg) and four different doses(0.5 mg,1 mg,2 mg,3 mg) of azelaic acid as adjuvant group,300 µL for each and one immunization.At the same time,set up the blank group,pure vaccine group,aluminum adjuvant control group.The sera from tail vein blood of mice were collected at the end of 4,8,12 and 16 weeks after immunization and the specific IgG antibody against HAV were detected by indirect ELISA method.Results In addition to the blank group,mice in various groups generated Anti-HAV IgG at 4,8,12,16 weeks after the immunization.The antibody levels increased as time went on and reached peak at the 8th and 12th week,then decreased gradually.At 4 weeks,the level of anti-hepatitis A virus (HAV) IgG produced by adjuvant group 4 (azelaic acid 3 mg) was significantly higher than aluminum adjuvant control group (P<0.05,t = 2.640).At the same time,the level of anti-hepatitis A virus (HAV) IgG in adjuvant group 4 was significantly higher at 4th week,8th week and 12th week than pure antigen group (P<0.05,t = 3.134,2.751,2.743).Conclusion Appropriate dose of azelaic acid can obviously enhance the HepA-1 induced humoral immune response in mice.Azelaic acid is expected to become a new adjuvant for human vaccines.

Key words: Azelaic acid, Vaccine adjuvant, Hepatitis A virus attenuated live vaccine(HepA-1)

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