Immune Disease Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 2010 Mar;84(5):2490-501. doi: 10.1128/JVI.02105-08. Epub 2009 Dec 16.
Dengue is a common arthropod-borne flaviviral infection in the tropics, for which there is no vaccine or specific antiviral drug. The infection is often associated with serious complications such as dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS), in which both viral and host factors have been implicated. RNA interference (RNAi) is a potent antiviral strategy and a potential therapeutic option for dengue if a feasible strategy can be developed for delivery of small interfering RNA (siRNA) to dendritic cells (DCs) and macrophages, the major in vivo targets of the virus and also the source of proinflammatory cytokines. Here we show that a dendritic cell-targeting 12-mer peptide (DC3) fused to nona-D-arginine (9dR) residues (DC3-9dR) delivers siRNA and knocks down endogenous gene expression in heterogenous DC subsets, (monocyte-derived DCs [MDDCs], CD34(+) hematopoietic stem cell [HSC])-derived Langerhans DCs, and peripheral blood DCs). Moreover, DC3-9dR-mediated delivery of siRNA targeting a highly conserved sequence in the dengue virus envelope gene (siFvE(D)) effectively suppressed dengue virus replication in MDDCs and macrophages. In addition, DC-specific delivery of siRNA targeting the acute-phase cytokine tumor necrosis factor alpha (TNF-alpha), which plays a major role in dengue pathogenesis, either alone or in combination with an antiviral siRNA, significantly reduced virus-induced production of the cytokine in MDDCs. Finally to validate the strategy in vivo, we tested the ability of the peptide to target human DCs in the NOD/SCID/IL-2Rgamma(-/-) mouse model engrafted with human CD34(+) hematopoietic stem cells (HuHSC mice). Treatment of mice by intravenous (i.v.) injection of DC3-9dR-complexed siRNA targeting TNF-alpha effectively suppressed poly(I:C)-induced TNF-alpha production by DCs. Thus, DC3-9dR can deliver siRNA to DCs both in vitro and in vivo, and this delivery approach holds promise as a therapeutic strategy to simultaneously suppress virus replication and curb virus-induced detrimental host immune responses in dengue infection.
登革热是热带地区常见的虫媒黄病毒感染,目前尚无疫苗或特效抗病毒药物。该感染常伴有严重并发症,如登革出血热(DHF)或登革休克综合征(DSS),病毒和宿主因素均与这些并发症有关。RNA 干扰(RNAi)是一种有效的抗病毒策略,如果能开发出将小干扰 RNA(siRNA)递送至树突状细胞(DC)和巨噬细胞的可行策略,那么它可能成为治疗登革热的一种潜在选择。DC 和巨噬细胞是病毒的主要体内靶标,也是促炎细胞因子的来源。本研究显示,与非a-D-精氨酸(9dR)残基融合的树突状细胞靶向 12 肽(DC3-9dR)可递呈 siRNA,并敲低异质 DC 亚群(单核细胞衍生的 DC[MDDC]、CD34+造血干细胞[HSC]衍生的朗格汉斯 DC 和外周血 DC)中的内源性基因表达。此外,DC3-9dR 介导的靶向登革病毒包膜基因高度保守序列的 siRNA(siFvE(D))递呈可有效抑制 MDDC 和巨噬细胞中的登革病毒复制。此外,单独或与抗病毒 siRNA 联合,靶向急性相细胞因子肿瘤坏死因子-α(TNF-α)的 DC 特异性 siRNA 递呈可显著降低 MDDC 中病毒诱导的细胞因子产生。最后,为了在体内验证该策略,我们在人 CD34+造血干细胞(HuHSC 小鼠)移植的 NOD/SCID/IL-2Rγ(-/-)小鼠模型中测试了该肽靶向人 DC 的能力。通过静脉(i.v.)注射 DC3-9dR 复合物靶向 TNF-α 的 siRNA 可有效抑制聚肌苷酸(poly(I:C))诱导的 DC 中 TNF-α 的产生。因此,DC3-9dR 既能在体外又能在体内将 siRNA 递送至 DC,这种递呈方法有望成为一种治疗策略,以同时抑制病毒复制并抑制登革热感染中病毒诱导的有害宿主免疫反应。