Zou Qiang, Wu Bing, He Xiaodan, Zhang Yizhi, Kang Youmin, Jin Jin, Xu Hanqian, Liu Hu, Wang Bin
State Key Laboratory for Agro-Biotechnology, Department of Microbiology and Immunology, College of Biological Science, China Agricultural University, Beijing 100193, China.
J Biomed Biotechnol. 2010;2010:562356. doi: 10.1155/2010/562356. Epub 2010 Apr 27.
Various chemokines and cytokines as adjuvants can be used to improve efficacy of DNA vaccination. In this study, we sought to investigate if a DNA construct expressing IL-9 (designed as proV-IL9) as a molecular adjuvant enhance antigen specific immune responses elicited by the pcD-VP1 DNA vaccination. Mice immunized with pcD-VP1 combined with proV-IL9 developed a strong humoral response. In addition, the coinoculation induced significant higher level of antigen-specific cell proliferation and cytotoxic response. This agreed well with higher expression level of IFN-gamma and perforin in CD8+ T cells, but not with IL-17 in these T cells. The results indicate that IL-9 induces the development of IFN-gamma-producing CD8+ T cells (Tc1), but not the IL-17-producing CD8+ T cells (Tc17). Up-regulated expressions of BCL-2 and BCL-XL were exhibited in these Tc1 cells, suggesting that IL-9 may trigger antiapoptosis mechanism in these cells. Together, these results demonstrated that IL-9 used as molecular adjuvant could enhance the immunogenicity of DNA vaccination, in augmenting humoral and cellular responses and particularly promoting Tc1 activations. Thus, the IL-9 may be utilized as a potent Tc1 adjuvant for DNA vaccines.
多种趋化因子和细胞因子作为佐剂可用于提高DNA疫苗接种的效果。在本研究中,我们试图探究表达IL-9的DNA构建体(设计为proV-IL9)作为分子佐剂是否能增强由pcD-VP1 DNA疫苗接种引发的抗原特异性免疫反应。用pcD-VP1与proV-IL9联合免疫的小鼠产生了强烈的体液反应。此外,联合接种诱导了显著更高水平的抗原特异性细胞增殖和细胞毒性反应。这与CD8+ T细胞中IFN-γ和穿孔素的较高表达水平相符,但与这些T细胞中的IL-17表达水平不符。结果表明,IL-9诱导产生IFN-γ的CD8+ T细胞(Tc1)的发育,但不诱导产生IL-17的CD8+ T细胞(Tc17)的发育。在这些Tc1细胞中表现出BCL-2和BCL-XL的上调表达,表明IL-9可能触发这些细胞中的抗凋亡机制。总之,这些结果表明,IL-9作为分子佐剂可增强DNA疫苗接种的免疫原性,增强体液和细胞反应,特别是促进Tc1激活。因此,IL-9可作为DNA疫苗的一种有效的Tc1佐剂。