Ohishi K, Kabeya H, Amanuma H, Onuma M
Laboratory of Gene Technology and Safety, Tsukuba Life Science Center, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.
Leukemia. 1997 Apr;11 Suppl 3:223-6.
In controlling retrovirus infection and replication, cell-mediated immunity (CMI) is considered to be effective. To develop a synthetic peptide vaccine capable of inducing CMI, mannan-coated liposome encapsulating 20-mer synthetic peptide, spanning the 98-117 amino acids of bovine leukemia virus (BLV) envelope glycoprotein (Env) gp51 was constructed and inoculated to BALB/c mice. The liposome induced specific delayed-type hypersensitivity, lymphocyte proliferative responses, and a weak cytotoxic lymphocyte response. The spleen cells from the immunized mice produced a large amount of IFN-gamma and IL-2, whereas they released neither IL-4 or IL-10. Mannan-coated liposome containing two kinds of peptides (the 121-140 and 142-161 regions of BLV Env gp51) also induced peptide-specific lymphocyte proliferative response and IFN-g production in C57BL/6 mice. Thus, the synthetic T-cell epitope peptide-liposome system augmented a strong Th-1 type immunity in mice.
在控制逆转录病毒感染和复制方面,细胞介导的免疫(CMI)被认为是有效的。为了开发一种能够诱导CMI的合成肽疫苗,构建了包裹20聚体合成肽的甘露聚糖包被脂质体,该合成肽跨越牛白血病病毒(BLV)包膜糖蛋白(Env)gp51的98 - 117个氨基酸,并将其接种到BALB/c小鼠体内。该脂质体诱导了特异性迟发型超敏反应、淋巴细胞增殖反应和较弱的细胞毒性淋巴细胞反应。免疫小鼠的脾细胞产生了大量的IFN-γ和IL-2,而它们既不释放IL-4也不释放IL-10。含有两种肽(BLV Env gp51的121 - 140和142 - 161区域)的甘露聚糖包被脂质体也在C57BL/6小鼠中诱导了肽特异性淋巴细胞增殖反应和IFN-γ产生。因此,合成的T细胞表位肽 - 脂质体系统增强了小鼠体内强大的Th-1型免疫。