期刊文献+

荆豆凝集素修饰的牛血清白蛋白脂质体的免疫学性质

Imuune evaluation of ulex europaeus agglutinin I modified liposomes loading bovine serum albumin
下载PDF
导出
摘要 目的对荆豆凝集素修饰的牛血清白蛋白脂质体进行免疫学评价。方法 3组小鼠分别于0、7、14、21 d口服免疫牛血清白蛋白溶液(bovine serum albumin,BSA)、BSA脂质体及荆豆凝集素修饰的BSA脂质体,建立ELISA法测定小鼠在7、14、21、28、35及42 d时体内产生的系统及黏膜免疫应答。结果与BSA溶液组相比,将抗原包裹于脂质体、尤其是荆豆凝集素修饰的脂质体中免疫小鼠后,可在小鼠血清及小肠分泌液中检测到较高的IgG及IgA水平。其中,免疫后42 d,凝集素修饰脂质体组的IgG和IgA水平分别为BSA溶液组产生相应抗体值的4.33倍和4.74倍。结论荆豆凝集素修饰脂质体口服免疫小鼠后可同时诱导机体产生黏膜及系统免疫应答,可以作为口服疫苗的载体。 Objective To establish the immune evaluation method of ulex europaeus agglutinin I modified liposomes loading bovine serum albumin. Methods Three groups of mice were respectively immunized by BSA solution ,LIP and UEAI-LIP. All animals received four immunization doses at 0,7,14 and 21 day and samples were collected after 7,14,21,28,35 and 42 days of primary immunization. Results Results indicate that antigen encapsulated in liposomes, especially the UEAI-modified ones, was favorable for inducing immune response. At 42 days after the first immunization, the highest IgG and IgA antibody levels produced by UEAI-LIP occurred, respectively showing 4.33-fold and 4. 74-fold higher levels compared to those of the groups receiving BSA alone. Conclusions UEAI-modified liposomes has high potential when used as carrier for oral vaccines.
出处 《沈阳药科大学学报》 CAS CSCD 北大核心 2013年第3期222-225,231,共5页 Journal of Shenyang Pharmaceutical University
关键词 脂质体 牛血清白蛋白 荆豆凝集素 免疫学评价 liposome bovine serum albumin ulex europaeus agglutinin I immune evaluation
  • 相关文献

参考文献13

  • 1CHRISTIANE B, CLAUS-MICHAE I, JOHN F W. Lectin-mediated drug targeting: history and applica- tions[J]. Advanced Drug Delivery Reviews,2004,56 (3) :425 -435.
  • 2刘亮,田宝成.生物黏附材料-植物凝集素及在制剂中的应用进展[J].中南药学,2007,5(2):164-167. 被引量:4
  • 3HUSSAIN N,JANI P U,FLORENCE A T. Enhanced oral uptake of tomato lectin-conjugated nanoparticles in the rat[J]. Pharm Res,1997,14(5) :613 -618.
  • 4杜修桥,胥传来,乐国伟,姚惠源.逆相蒸发法制备猪用生长激素脂质体工艺的优化研究[J].中国油脂,2003,28(3):47-50. 被引量:5
  • 5蔡勤,孟延发,张志荣.5-氟尿嘧啶-花生凝集素结合物的制备与结合率测定[J].生物医学工程学杂志,2005,22(3):545-547. 被引量:4
  • 6ISABEL E,MIGUEL A. Preparation of Ulex europae- us lectin-gliadin nanoparticle conjugates and their in- teraction with gastrointestinal mucus [ J ]. International Journal of Pharmaceutics, 1999,191:25 - 32.
  • 7SEIICHIRO M, KAZUNORI I. Application of poly- ethyleneglycol (PEG)-modified liposomes for oral vaccine:effect of lipid dose on systemic and mucosal immunity [ J ]. Journal of Controlled Release, 2003, 89:189 - 197.
  • 8TAKUYA I, SHINOBU W. Humoral immune re- sponse induced by oral immunization with liposome- entrapped antigen [ J ]. Developmental and Compara- tive Immunology ,2003,27:413 - 421.
  • 9BAINTNER K, JAKAB G, GYORI Z. Binding of FITC-labelled lectins to the gastrointestinal epithelium of the rat [ J ]. Pathol Oncol Res, 2000,6 ( 3 ) : 179 - 183.
  • 10CLARK M A, JEPSON M A, HIRST B H. Lectin binding defines and differentiates M-cells in mouse small intestine and caecum [J]. Histochem Cell Biol, 1995,104(2) :161 - 168.

二级参考文献46

共引文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部