Fiedler M, Lu M, Siegel F, Whipple J, Roggendorf M
Institute of Virology, University Clinic Essen, Hufelandstrasse 55, D-45122, Essen, Germany.
Vaccine. 2001 Sep 14;19(32):4618-26. doi: 10.1016/s0264-410x(01)00245-6.
We investigated the DNA immunization approach in order to induce a protective immune response against hepatitis delta virus (HDV) superinfection of chronically woodchuck hepatitis virus (WHV) infected woodchucks. The animals were immunized with an expression vector encoding HDAg by gene gun. T cell and humoral immune responses induced by this protocol were determined and compared with those induced by HDAg immunization using a CpG oligonucleotide as an adjuvant. After immunization the woodchucks were challenged with 10(6) genome equivalents of HDV. The protein immunization with HDAg induced good humoral and T helper cell responses in the woodchucks, but did not protect them from HDV superinfection. The DNA immunized woodchucks were also not protected from HDV superinfection, however, the course of infection was modified: HDV viremia occurred later, the typical fluctuation of the HDV RNA titer with several peaks was absent, and antibodies to HDV were not detectable.
我们研究了DNA免疫方法,以诱导针对慢性土拨鼠肝炎病毒(WHV)感染的土拨鼠发生丁型肝炎病毒(HDV)重叠感染的保护性免疫反应。通过基因枪用编码HDAg的表达载体对动物进行免疫。确定了该方案诱导的T细胞和体液免疫反应,并与使用CpG寡核苷酸作为佐剂的HDAg免疫诱导的反应进行了比较。免疫后,用10⁶个HDV基因组当量攻击土拨鼠。用HDAg进行蛋白质免疫在土拨鼠中诱导了良好的体液和辅助性T细胞反应,但不能保护它们免受HDV重叠感染。DNA免疫的土拨鼠也不能免受HDV重叠感染,然而,感染过程有所改变:HDV病毒血症出现得较晚,HDV RNA滴度没有典型的有多个峰值的波动,并且未检测到抗HDV抗体。