Department of Pathology & Molecular Medicine and McMaster Immunology Research Centre, McMaster University, Hamilton, ON L8S 4K1, Canada.
Department of Pharmaceutical Sciences, College of Pharmacy, Texas A&M University, College Station, TX 77843, USA.
Int J Mol Sci. 2020 Jan 4;21(1):337. doi: 10.3390/ijms21010337.
Herpes Simplex Virus Type 2 (HSV-2) is one of the most prevalent sexually transmitted viruses and is a known risk factor for HIV acquisition in the Female Genital Tract (FGT). Previously, we found that curcumin can block HSV-2 infection and abrogate the production of inflammatory cytokines and chemokines by genital epithelial cells in vitro. In this study, we investigated whether curcumin, encapsulated in nanoparticles and delivered by various in vivo routes, could minimize inflammation and prevent or reduce HSV-2 infection in the FGT. Female mice were pre-treated with curcumin nanoparticles through oral, intraperitoneal and intravaginal routes, and then exposed intravaginally to the tissue inflammation stimulant CpG-oligodeoxynucleotide (ODN). Local intravaginal delivery of curcumin nanoparticles, but not intraperitoneal or oral delivery, reduced CpG-mediated inflammatory histopathology and decreased production of pro-inflammatory cytokines Interleukin (IL)-6, Tumor Necrosis Factor Alpha (TNF-α) and Monocyte Chemoattractant Protein-1 (MCP-1) in the FGT. However, curcumin nanoparticles did not demonstrate anti-viral activity nor reduce tissue pathology when administered prior to intravaginal HSV-2 infection. In an alternative approach, intravaginal pre-treatment with crude curcumin or solid dispersion formulations of curcumin demonstrated increased survival and delayed pathology following HSV-2 infection. Our results suggest that curcumin nanoparticle delivery in the vaginal tract could reduce local tissue inflammation. The anti-inflammatory properties of curcumin delivered to the vaginal tract could potentially reduce the severity of HSV-2 infection and decrease the risk of HIV acquisition in the FGT of women.
单纯疱疹病毒 2 型 (HSV-2) 是最常见的性传播病毒之一,也是女性生殖道 (FGT) 中 HIV 获得的已知风险因素。先前,我们发现姜黄素可以阻断 HSV-2 感染,并在体外阻断生殖道上皮细胞产生炎症细胞因子和趋化因子。在这项研究中,我们研究了姜黄素纳米颗粒是否可以通过各种体内途径封装并输送,以最小化炎症并预防或减少 FGT 中的 HSV-2 感染。通过口服、腹腔内和阴道内途径预先用姜黄素纳米颗粒处理雌性小鼠,然后阴道内暴露于组织炎症刺激物 CpG-寡脱氧核苷酸 (ODN)。局部阴道内递送姜黄素纳米颗粒,而不是腹腔内或口服递送,可减少 CpG 介导的炎症组织病理学,并减少 FGT 中促炎细胞因子白细胞介素 (IL)-6、肿瘤坏死因子-α (TNF-α) 和单核细胞趋化蛋白-1 (MCP-1) 的产生。然而,姜黄素纳米颗粒在阴道内 HSV-2 感染之前给药时并未显示抗病毒活性,也未减轻组织病理学变化。在另一种方法中,阴道内预先用粗姜黄素或姜黄素固体分散体制剂处理可提高 HSV-2 感染后的存活率并延迟病理学变化。我们的结果表明,阴道内姜黄素纳米颗粒的递送达可能会减少局部组织炎症。递送到阴道的姜黄素的抗炎特性可能会降低 HSV-2 感染的严重程度,并降低女性 FGT 中 HIV 获得的风险。