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应用四环素调控系统建立可调控抗恶性疟原虫DNA疫苗的初步研究
引用本文:雷俊川,缪军,李珣,Kai Schonig,Hermann Bujard,薛采芳. 应用四环素调控系统建立可调控抗恶性疟原虫DNA疫苗的初步研究[J]. 细胞与分子免疫学杂志, 2004, 20(3): 356-359
作者姓名:雷俊川  缪军  李珣  Kai Schonig  Hermann Bujard  薛采芳
作者单位:1. 第四军医大学病原生物学教研室,陕西,西安,710032
2. 海德堡大学分子生物学中心,德国,海德堡,D-69120
摘    要:目的 :应用四环素 (tetracycline,Tet)可调控系统建立可调控的抗恶性疟原虫的DNA疫苗。方法 :首先构建恶性疟原虫顶端膜抗原 1(AMA 1)基因和转录激活因子 (tTA或rtTA)基因的真核表达质粒pTL 8/AMA 1和pTL 8/AMA 1(rtTA) ,并大量制备这两种质粒及表达转录抑制子 (tTS)的质粒pUHS6 1。以pTL 8/AMA 1、pTL 8/AMA 1(rtTA)和pTL 8/AMA 1(rtTA)加pUHS6 1/tTS免疫小鼠后 ,用四环素类似物强力霉素 (doxcycline ,dox)诱导或抑制上述DNA载体内AMA 1的表达 ,并分离小鼠血清检测针对AMA 1抗体的表达情况。结果 :①构建了真核表达质粒pTL 8/AMA 1和pTL 8/AMA 1(rtTA) ;②pTL 8/AMA 1和pTL 8/AMA 1(rtTA)在没有被诱导表达时 (仅基础表达 ) ,可诱导明显的免疫应答。在以pTL 8/AMA 1(rtTA)与含tTS的pUHS6 1共同免疫后 ,可极大地降低其免疫应答。应用dox诱导pTL 8/AMA 1(rtTA)中的AMA 1基因表达后 ,可明显引起免疫应答。结论 :pTL 8/AMA 1(rtTA)附加pUHS6 1构成了可调节的DNA免疫系统。该系统的建立将对进一步深入研究DNA疫苗的免疫机制和调控基因表达 ,减少不良免疫反应以及进行可精确调控的基因治疗打下一定的基础

关 键 词:四环素可调控系统  DNA疫苗  顶端膜抗原1
文章编号:1007-8738(2004)03-0356-04
修稿时间:2004-01-09

Preliminary study on regulable DNA vaccines against Plasmodium falciparum
Jun-chuan Lei,Jun Miao,Xun Li,Kai Schonig,Hermann Bujard,Cai-fang Xue. Preliminary study on regulable DNA vaccines against Plasmodium falciparum[J]. Chinese journal of cellular and molecular immunology, 2004, 20(3): 356-359
Authors:Jun-chuan Lei  Jun Miao  Xun Li  Kai Schonig  Hermann Bujard  Cai-fang Xue
Affiliation:Department of Pathogenic Biology, Fourth Military Medical University, Xi'an 710032, China. leijunc2002@yahoo.com.cn
Abstract:AIM: To construct regulable DNA vaccine against Plasmodium falciparum by using tetracycline(Tet) regulable system. METHODS: Eukaryotic expression vectors pTL 8/apical membrane antigen 1 (AMA 1) (tTA) and pTL 8/AMA 1(rtTA)gene which express trans activator (tTA) or reverse trans activator(rtTA), respectively, and AMA 1 gene of Plasmodium falciparum were constructed. BALB/c mice were immunized with these plasmids and doxycycline (dox) was administered to regulate the expression of AMA 1. For some mice immunized with pTL 8/AMA 1(rtTA), pUHS6 1, a plasmid containing trans silencer (tTS) to suppress basal expression of AMA 1 from pTL 8/AMA 1(rtTA), was injected into these mice together with pTL 8/AMA 1(rtTA). The sera of the mice were isolated at 2,4,6 and 8 weeks post immunization and the antibodies specific to AMA 1 were measured by ELISA. RESULTS: pTL 8/AMA 1 and pTL 8/AMA 1(rtTA) were constructed successfully. The mice immunized by pTL 8/AMA 1(tTA) with dox or by pTL 8/AMA 1(rtTA) without dox (at these conditions, AMA 1 was expressed at basal level)developed significant antibodies against AMA 1. Mice immunized by pTL 8/AMA 1(rtTA)and pUHS6 1 without dox did not develop significantly antibodies against AMA 1. In contrast, the mice immunized by pTL 8/AMA 1(rtTA)and pUHS6 1 with dox produced high level of antibodies. CONCLUSION: pTL 8/AMA 1(rtTA)combined with pUHS6 1 is a good regulable DNA vaccine candidate against Plasmodium falciparum .
Keywords:Tet regulable system  DNA vaccine  AMA 1
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