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作 者:高明[1] 王海平[2] 卢媛[1] 周勇[2] 王燕宁[1] 詹林盛[2] 王全立
机构地区:[1]兰州军区兰州总医院输血科,兰州730050 [2]军事医学科学院野战输血研究所,北京100850 [3]3307医院输血科,北京100071
出 处:《中国生物制品学杂志》2010年第3期234-237,共4页Chinese Journal of Biologicals
基 金:国家自然科学基金资助项目(30200245)
摘 要:目的构建基于Ii分子的丙型肝炎病毒(HCV)内源性靶向基因疫苗质粒,并检测其在真核细胞中的表达及免疫小鼠诱导的体液免疫应答。方法通过3轮PCR,以HCV-NS3的Th1表位(1248~1261aa)取代Ii链CLIP片段编码基因,构建基于Ii分子的HCV内源性靶向基因疫苗质粒,转染COS-7细胞,RT-PCR法检测其在mRNA水平的表达;用内源性靶向基因疫苗pHCV-NS3-Th1和非靶向基因疫苗pHCV-NS3经股四头肌肌肉免疫BALB/c小鼠,以生理盐水、pCI-neo和pCI-neo-Ii作为对照,检测小鼠的体液免疫应答水平。结果转染细胞中,内源性靶向基因疫苗质粒在mRNA水平获得表达;对BALB/c小鼠的免疫结果显示,只有pHCV-NS3组小鼠可以检测到针对HCV-NS3的特异性抗体,抗体滴度可达1:1024。结论已成功构建了基于Ii分子的HCV内源性靶向基因疫苗质粒,其能够在真核细胞中表达,但不能刺激小鼠产生HCV-NS3特异性抗体。Objective To construct a plasmid vaccine based on invariant chain CLIP substitution,express in eukaryotic cells and induce humoral immune response in mice.Methods HCV-NS3 Th1 plasmid vaccine was constructed by substitution of the gene encoding CLIP fragment of invariant chain(I)iwith the Th1 epitope(1248~1261aa)of HCV-NS3 through three cycles of PCR,then transfected to COS-7 cells and determined for expression by RT-PCR.BALB/c mice were immunized i.m.with the constructed vaccine pHCV-NS3-Th1 and non-targeting gene vaccine pHCV-NS3 respectively,using physiological saline,pCI-neo and pCI-neo-Ii as control,and determined for humoral immune response levels.Results The constructed plasmid vaccine pHCV-NS3-Th1 was expressed in transfected cells at mRNA level.However,the specific antibody against HCV-NS3,at a titer of 1:1 024,was only detected in the mice immunized with pHCV-NS3.Conclusion The plasmid vaccine based on invariant chain CLIP substitution was successfully constructed and expressed in eukaryotic cells,but induced no specific antibody against HCV-NS3 in mice.
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