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作 者:赵焕阁[1] 林映莹[1] 黄用豪[1] 黄风迎[1] 周松林[1] 刘中娟[2] 谭光宏[1] 韦祎[3]
机构地区:[1]海南医学院海南省热带病重点实验室,海口571101 [2]海南医学院干细胞研究所,海口571101 [3]海南医学院中医学院,海口571101
出 处:《中国人兽共患病学报》2013年第5期486-489,共4页Chinese Journal of Zoonoses
基 金:海南省自然科学基金(No.809018)资助
摘 要:目的观察弓形虫ROP5基因疫苗和基因免疫佐剂IL-12共免疫对昆明小鼠所诱导的免疫保护性。方法大量制备重组质粒pcROP5和pcmIL-12,以100μg的剂量同时免疫昆明小鼠,PBS组和pcDNA3.1空质粒组作为对照。用ELISA法测定免疫鼠血清中特异性抗体IgG、IgG亚型的表达水平及细胞因子IFN-γ、IL-4的含量,MTT法测定淋巴细胞转化率,观察小鼠受攻击感染弓形虫后的存活时间。结果质粒pcROP5和pcmIL-12共免疫小鼠3次后,与pcROP5质粒单独免疫组和对照组相比,IL-12基因佐剂的共免疫提高了免疫鼠血清中特异性抗体IgG及IgG亚型IgG2a的表达水平,提高了细胞因子IFN-γ的含量,增加了淋巴细胞的转化率,但IgG1和IL-4的表达水平变化不大;攻击感染后,质粒pcROP5和pc-mIL-12共免疫组小鼠存活时间显著延长。结论弓形虫ROP5基因与基因佐剂pcmIL-12共免疫能增强对小鼠的免疫保护性。The purpose of this study was to examine the iramunoprotection effect induced by ROP5 DNA vaccine with co-immunization of a plasmid encoding IL-12 (pcmIL-12) as an adjuvant in Kunming mice against Toxoplasma gondii. Mice were co-injected ROP5 with IL-12 at the dosage of 100 μg, controls mice were inoculated with PBS and the empty plasmid pcD- NA3.1 respectively. Levels of IgG antibody, IgG isotype, gamma interferon (IFN-γ), and interleukin-4 were detected by EL1SA. MTT assay was used to tested splenocyte proliferation. All mice were challenged with tachyzoites of the virulent T. gondii RH strain after the last immunization to observe the survival time. In this study we detected the higher level of IgG anti- body and cytokine IFN-γ in mice after three immunizations by pcROP5 co-immunized with pcmIL-12 compared to pcROP5 group and control groups. In respect to the IgG isotypes, co-immunization with pcmII.-2 enhanced the level of IgG2a, while IgG1 and IL-4 level was not appreciably different. After a lethal challenge of T. gondii RH strain, survival time of the mice co- immunized with pcmII.-12 was prolonged compared to the control groups. Immune responses could be enhanced by ROP5 co- immunized with IL-12 genetic adjuvant.
关 键 词:DNA疫苗 弓形虫抗原ROP5 基因佐剂pcmIL-12 免疫应答
分 类 号:R382[医药卫生—医学寄生虫学]
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