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作 者:王莉馨[1] 金宁一[1] 王宏伟[1] 秦云龙[1] 罗坤[1] 葛涛[1] 江文正[1] 金洪涛[1]
机构地区:[1]解放军军需大学研究所解放军基因工程重点实验室,长春130062
出 处:《中国免疫学杂志》2002年第5期297-300,共4页Chinese Journal of Immunology
基 金:国家杰出育年基金(39770661)资助
摘 要:目的:将HIV-1中国流行株B亚型gag基因、gag和hIL-2基因在天坛株痘苗病毒中进行共表达,以期获得重组痘苗病毒,观察细胞因子的佐剂作用,与核酸疫苗混合免疫,评价免疫效果,为新型艾滋病疫苗研制开发打下基础。方法:将HIV-1中国流行株 gag基因、gag和hIL-2基因片段插入到 pJ38载体启动子下游,经同源重组和血凝素阴性空斑筛选重组痘苗病毒,SDS-PAGE、Western blot检测目的蛋白。以重组病毒和核酸疫苗免疫Balb/c小鼠,进行淋巴细胞转化实验、CTL、CD4+、CD8+ T细胞数目以及血清抗体的细胞免疫和体液免疫指标检测。结果:获得了重组痘苗病毒 vJ38gag和 vJ38gag-IL-2。与 vJ38-gag相比,vJ38gag-IL-2,具有更好的免疫原性,重组痘苗病毒免疫3次的效果好于重组病毒免疫2次,以2rVV-DNA混合免疫效果最好。结论:重组痘苗病毒vJ38gag和vJ38gag-IL-2能够表达外源蛋白并诱导机体产生细胞免疫和体液免疫。细胞因子IL-2发挥了免疫佐剂的作用。Abstract Objective:To obtain recombinant vaccinia viruses expressed HIV-lcn subtype B gag and gag-hIL-2 chimera gene,evaluate theimmune effects in experimental mice by immunization with HIV-1 DNA vaccine,observe the immune adjuvant effect of IL-2.Metbods: HIV0-1gag and gag-hIL-2 chimera gene were inserted downstream of the combined promotor of pJ38 vector respectively and recombinant vaccinia virus-es were selected by plaque essay. Expression products were examined by SDS-PAGE and Western blot.Immune response of immunized Balb/cmice was evaluated by lymphocyte transformation test,CTL quantity change of T lymphocyte of CD4+、CD8+ and the level of serum antibody.Re-sults:Recombinant vaccinia viruses vJ38gag and vJ38gag-IL-2 were obtained and the expression were confirmed by SDS-PAGE and Western-blot. Recombinant vaccinia viruses show good immune effect when immuned with HIV-1 DNA vaccine.The best strategy for immunization is therVV-primed and HIV-1 DNA vaccine-boosted group and threer times of immunization were suggested to get effective results compared withvJ38gag an incressed immune response was induced by vJ38gag-IL-2. Conclusion: HIV-1 Gag protein and IL-2 protein can be expressed invJ38gag and vJ38gag-IL-2 respectively. IL-2 show good effect to ha sued as immune adjuvant.
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