Interleukin-10 Antisense Oligodeoxynucleotide Suppresses IL-10 Expression and Effects on Proinflammatory Cytokine Responses to Porcine Reproductive and Respiratory Syndrome Virus

被引:15
作者
Charerntantanakul, Wasin [1 ]
Kasinrerk, Watchara [2 ,3 ]
机构
[1] Maejo Univ, Fac Sci, Dept Biol, Chiang Mai 50290, Thailand
[2] Chiang Mai Univ, Div Clin Immunol, Dept Med Technol, Fac Associated Med Sci, Chiang Mai 50000, Thailand
[3] Chiang Mai Univ, Biomed Technol Res Ctr, Natl Ctr Genet Engn & Biotechnol, Natl Sci & Technol Dev Agcy,Fac Associated Med Sc, Chiang Mai 50000, Thailand
关键词
ANTIGEN-PRESENTING CELLS; INFECTED IN-UTERO; DENDRITIC CELLS; GENE-EXPRESSION; IMMUNE-RESPONSES; T-CELLS; RNA INTERFERENCE; ENDOGENOUS IL-10; MESSENGER-RNA; UP-REGULATION;
D O I
10.1089/vim.2009.0066
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. Naive 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 CD8 beta(+) T cells. Our results suggest that IL-10AS has the potential to enhance proinflammatory cytokine responses to PRRSV infection.
引用
收藏
页码:425 / 435
页数:11
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