, 2014). In the NEUTRINO phase III trial of treatment-naive patients, 12 weeks of triple combination therapy with sofosbuvir (400 mg) once daily resulted in SVR rates of 89% in patients with HCV genotype 1 (92% for subtype 1a and 82% for subtype 1b), and 96% in patients with genotype 4 (Lawitz et al., 2013). Moreover, in the FISSION trial of HCV-2/3 treatment-naive patients receiving sofosbuvir/RBV

for 12 weeks, 95% of patients with genotype 2 and 56% of patients with genotype 3 achieved an SVR (Lawitz et al., 2013). In addition, most DAA agents are characterised by a low genetic barrier to the development of resistance, except sofosbuvir, which CH5424802 datasheet showed a very high resistance barrier. This is the reason most current DAA-based therapies under evaluation must be co-administered with either PEG-IFN-alpha and ribavirin or different compounds belonging to different DAA classes (Poveda et al., 2014). Pycnogenol® (PYC; trademark

of Horphag Research, Geneva, Switzerland) is a French maritime pine extract produced from the outer bark of Pinus pinaster ssp. atlantica, and is generally considered safe for human use ( American Botanical Council, 2010). The main PYC constituents are procyanidins (68.4%), taxifolin (21.87%), ferulic acid (3.70%), catechin (2.53%), and caffeic acid (3.51%) ( Lee et al., 2010). PYC has been reported to have DAPT antioxidative and anti-inflammatory effects, and to reduce cardiovascular risk factors associated with type 2

diabetes ( Maimoona et al., 2011 and Zibadi et al., 2008). A recent report suggests that PYC can inhibit encephalomyocarditis virus replication in the mouse heart by suppressing expression of proinflammatory Ribonucleotide reductase cytokines, and genes related to cardiac remodelling and mast cells ( Matsumori et al., 2007). PYC has also been reported to inhibit binding of human immunodeficiency virus type-1 to host cells, and to cause other significant changes, including increased expression of manganese superoxide dismutase ( Feng et al., 2008). HCV gene expression elevates reactive oxygen species (ROS) levels via calcium signalling. In addition, HCV Core, NS3, and NS5A proteins have all been shown to induce oxidative stress (Choi et al., 2004). The reported link between HCV and oxidative stress makes this pathway a promising anti-HCV therapeutic strategy. To date, however, the effect of PYC on HCV infection has not been investigated. This study evaluated the inhibitory effects of Pycnogenol® on HCV replication in vitro and in vivo. Genotype 1b HCV subgenomic replicon cell lines, R6FLR-N (R6, genotype 1b, strain N) (Watanabe et al., 2006), FLR3-1 (genotype 1b, Con-1) (Sakamoto et al., 2005) and Rep JFH Luc3-13 genotype 2a (Takano et al.