CpG寡核苷酸
生物
TLR9型
抗原
分子生物学
白细胞介素21
抗原提呈细胞
CD28
白细胞介素12
细胞毒性T细胞
单克隆抗体
细胞生物学
T细胞
CpG站点
体外
免疫学
抗体
免疫系统
基因表达
生物化学
DNA甲基化
基因
作者
Sylvia Bendigs,Ulrich Salzer,Grayson B. Lipford,Hermann Wagner,Klaus Heeg
标识
DOI:10.1002/(sici)1521-4141(199904)29:04<1209::aid-immu1209>3.0.co;2-j
摘要
CpG-containing oligodeoxynucleotides (CpG-ODN) act as powerful adjuvant during in vivo induction of T cell responses. While CpG-ODN directly activate antigen-presenting cells (APC) and thus exert an extrinsic activity on T cells, it is unclear whether they directly affect T cells (intrinsic activity). Here we analyze the effects of CpG-ODN on T cells in an APC-free cell culture. We report that CpG-ODN co-stimulate T cells provided they were triggered via their TCR. CpG-ODN induced IL-2 production, IL-2 receptor expression and thus proliferation. Proliferation was blocked by cyclosporin A or anti-IL-2 monoclonal antibodies (mAb) but not by anti-IL-4 mAb. Moreover, CpG-co-stimulated T cells differentiated into cytolytic T lymphocytes in vitro. Of note, IL-2-driven growth of primed T cells was not affected by CpG-ODN. Co-stimulation was also operative in T cells from CD28− / − mice and in TCR-transgenic T cells stimulated with peptide. CpG-ODN-mediated co-stimulation of T cells in vitro may thus explain part of the potent adjuvant effects of CpG-ODN in vivo.
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