Department of Biology, Faculty of Science, Maejo University, Chiang Mai, Thailand.
Viral Immunol. 2010 Aug;23(4):425-35. doi: 10.1089/vim.2009.0066.
Upregulation of interleukin-10 (IL-10) expression has been suggested to be the mechanism by which the porcine reproductive and respiratory syndrome virus (PRRSV) suppresses the innate and adaptive immune response in infected pigs. In this study we evaluated the potential of phosphorothioate-modified IL-10 antisense oligodeoxynucleotide specific to the translation initiation region of porcine IL-10 mRNA (IL-10AS) in enhancing proinflammatory cytokine responses to PRRSV. Naïve peripheral blood mononuclear cells from eight PRRSV-seronegative pigs were transfected with IL-10AS in vitro prior to PRRSV inoculation and phorbol 12-myristate 13-acetate plus ionomycin or concanavalin A stimulation. The effects of IL-10AS on mRNA expression of IL-10, interferon-gamma (IFN-gamma), IFN-alpha, tumor necrosis factor-alpha (TNF-alpha), IL-2, and IL-4 were tested by real-time PCR. The percentages of IFN-gamma-producing T-cell subsets were determined by flow cytometry. Compared to the controls, the levels of IL-10 and IL-2 mRNA were significantly reduced, while those of IFN-gamma mRNA were increased, and TNF-alpha, IFN-alpha, and IL-4 mRNA were unchanged. An increase in the percentage of the IFN-gamma+ population was also observed in lymphocytes and CD8beta+ T cells. Our results suggest that IL-10AS has the potential to enhance proinflammatory cytokine responses to PRRSV infection.
白细胞介素-10(IL-10)表达的上调被认为是猪繁殖与呼吸综合征病毒(PRRSV)抑制感染猪固有和适应性免疫反应的机制。在这项研究中,我们评估了针对猪 IL-10 mRNA 翻译起始区的硫代磷酸酯修饰的 IL-10 反义寡脱氧核苷酸(IL-10AS)在增强 PRRSV 感染后促炎细胞因子反应的潜力。从 8 头 PRRSV 血清阴性的猪中分离出外周血单个核细胞,在 PRRSV 接种前进行 IL-10AS 体外转染,并进行佛波醇 12-肉豆蔻酸 13-乙酸酯加离子霉素或刀豆蛋白 A 刺激。通过实时 PCR 检测 IL-10AS 对 IL-10、干扰素-γ(IFN-γ)、IFN-α、肿瘤坏死因子-α(TNF-α)、IL-2 和 IL-4 的 mRNA 表达的影响。通过流式细胞术测定 IFN-γ产生 T 细胞亚群的百分比。与对照组相比,IL-10 和 IL-2 mRNA 的水平显著降低,而 IFN-γ mRNA 的水平增加,TNF-α、IFN-α 和 IL-4 mRNA 的水平不变。淋巴细胞和 CD8β+T 细胞中 IFN-γ+群体的百分比也增加。我们的结果表明,IL-10AS 有可能增强 PRRSV 感染后的促炎细胞因子反应。