Departmemt of Bioregulatory Medicine, Ehime University Graduate School of Medicine, Toon, Ehime, Japan.
Virol J. 2010 May 10;7:91. doi: 10.1186/1743-422X-7-91.
Human herpesvirus 6 (HHV-6) has a tropism for immunocompetent cells, including T lymphocytes, monocytes/macrophages, and dendritic cells (DCs) suggesting that HHV-6 infection affects the immunosurveillance system. Toll-like receptor (TLR) system plays an important role in innate immunity against various pathogens. In the present study, we investigated the effect of HHV-6 infection on the expression and intracellular signaling of TLRs in DCs. Although expression levels of TLRs were not decreased or slightly elevated following HHV-6 infection, the amounts of cytokines produced following stimulation with ligands for TLRs appeared to be dramatically decreased in HHV-6-infected DCs as compared to mock-infected DCs. Similarly, phosphorylation levels of TAK-1, IkappaB kinase, and IkappaB-alpha following stimulation of HHV-6-infected DCs with lipopolysaccharide, which is the ligand for TLR4, appeared to be decreased. These data show that HHV-6 impairs intracellular signaling through TLRs indicating the novel mechanism of HHV-6-mediated immunomodulation.
人类疱疹病毒 6(HHV-6)对免疫活性细胞具有嗜性,包括 T 淋巴细胞、单核细胞/巨噬细胞和树突状细胞(DC),这表明 HHV-6 感染会影响免疫监视系统。Toll 样受体(TLR)系统在针对各种病原体的固有免疫中发挥重要作用。在本研究中,我们研究了 HHV-6 感染对 DC 中 TLR 表达和细胞内信号转导的影响。尽管 HHV-6 感染后 TLR 的表达水平没有降低或略有升高,但与 mock 感染的 DC 相比,HHV-6 感染的 DC 中 TLR 配体刺激后产生的细胞因子量明显减少。同样,HHV-6 感染的 DC 用脂多糖(TLR4 的配体)刺激后,TAK-1、IkappaB 激酶和 IkappaB-alpha 的磷酸化水平似乎降低。这些数据表明 HHV-6 通过 TLR 损害细胞内信号转导,提示 HHV-6 介导的免疫调节的新机制。