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具有 CCT 重复序列的人源微卫星 DNA 模拟寡脱氧核苷酸通过选择性 TLR 通路负调控 TLR7/9 介导的固有免疫反应。

A human microsatellite DNA-mimicking oligodeoxynucleotide with CCT repeats negatively regulates TLR7/9-mediated innate immune responses via selected TLR pathways.

机构信息

Department of Immunology, Jilin University, Changchun, China.

出版信息

Clin Immunol. 2010 Mar;134(3):262-76. doi: 10.1016/j.clim.2009.11.009. Epub 2010 Jan 19.

Abstract

A human microsatellite DNA-mimicking ODN (MS ODN) composed of CCT repeats, designated as SAT05f, has been studied for its capacity of negatively regulating innate immunity induced by TLR7/TLR9 agonists in vitro and in mice. The result showed that SAT05f could down-regulate TLR7/9-dependent IFN-alpha production in cultured human PBMC stimulated by inactivated Flu virus PR8 or HSV-1 or CpG ODN or imiquimod, protect d-GalN-treated mice from lethal shock induced by TLR9 agonist, not by TLR3/4 agonist. In addition, SAT05f significantly inhibit IFN-alpha production from purified human plasmacytoid cells (pDCs) stimulated by CpG ODN. Interestingly, SAT05f could up-regulate CD80, CD86, and HLA-DR on the pDCs in vitro, implying that SAT05f-mediated inhibition on IFN-alpha production could be related to the activation of pDCs. The data suggest that SAT05f could be developed as a candidate medicament for the treatment of TLR7/9 activation-associated diseases by inhibiting TLR7/9 signaling pathways.

摘要

一种由 CCT 重复序列组成的人源微卫星 DNA 模拟寡核苷酸(MS ODN),被命名为 SAT05f,已被研究用于其体外和在小鼠中负调节 TLR7/TLR9 激动剂诱导的固有免疫的能力。结果表明,SAT05f 可下调经灭活 Flu 病毒 PR8 或 HSV-1 或 CpG ODN 或咪喹莫特刺激的培养的人 PBMC 中 TLR7/9 依赖性 IFN-α的产生,保护 d-GalN 处理的小鼠免受 TLR9 激动剂诱导的致命性休克,但不受 TLR3/4 激动剂的影响。此外,SAT05f 可显著抑制 CpG ODN 刺激的纯化人浆细胞样树突状细胞(pDCs)中 IFN-α的产生。有趣的是,SAT05f 可在体外上调 pDCs 上的 CD80、CD86 和 HLA-DR,这表明 SAT05f 介导的 IFN-α产生抑制可能与 pDCs 的激活有关。这些数据表明,SAT05f 可通过抑制 TLR7/9 信号通路,作为治疗 TLR7/9 激活相关疾病的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8be6/7106173/680c70edebf3/gr1_lrg.jpg

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