2.?Materials and Methods2.1. Cell isolation (pDC and NK cells)PBMC from single-donor buffy coat blood packs (National Blood Transfusion Service, UK) were isolated by Histopaque (Sigma-Aldrich, UK) density centrifugation then separated through a 50% percoll (Sigma-Aldrich, UK) gradient (30 min at 300 g). pDC were magnetically isolated from the interface of the percoll gradient using BDCA-4 microbeads (Miltenyi Biotec, Germany) in accordance with the manufacturer’s protocol. Autologous NK cells were purified from the lymphocyte fraction at the bottom of the gradient by positive magnetic separation using CD56 microbeads (Miltenyi Biotec, Germany) followed by depletion of NKT cells using anti-CD3 conjugated Dynal beads, and were frozen in FCS containing 10% dimethyl sulfoxide (DMSO) (Sigma-Aldrich, UK) for later use.

2.2. Co-culturesImmature and mature pDC populations were used for co-culture with autologous NK cells. Freshly isolated blood pDC cultured in the presence of IL-3 for 24 hours were used as immature DC. Mature pDC were generated by stimulating freshly isolated blood pDC with 6 ��g/mL CpG ODN (G*G*GGGACGATCGTCG*G*G*G*G*G, Oswel, UK) [7] for 24 hours in the presence of IL-3. Previous studies have shown that, compared to pDC maintained in IL-3 alone, pDC stimulated with CpG show a more dendritic morphology and express higher levels of co-stimulatory molecules [22]. pDC were washed before co-culture with autologous NK cells (at a ratio of 1:5) for a further 24 hours. DC-NK cell culture supernatants were removed and stored at -20��C for cytokine assay by ELISA.

Anacetrapib In some experiments NK cells were incubated with a type I IFN receptor blocking antibody (10 ��g/mL, or otherwise indicated) (R&D Systems, UK) for 20 minutes on ice, prior to co-culture with DC. In other experiments, NK cells were incubated for 24 hours with rhIFN�� (1 ��g/mL, Sigma-Aldrich, UK), or with supernatants from pDC that were cultured in the presence of IL-3, or IL-3 and CpG DNA for 24 hours. As a positive control of activation, NK cells were cultured in the presence of IL-2 (50 units/mL, R&D Systems, Abingdon, UK), influenza virus (H3N2 strain X-31), or with PMA (50 ng/mL) and Ionomycin (1 ��M) (both from Sigma-Aldrich, UK).2.3. Phenotypic characterisationSurface antigen expression was analysed by three or four-colour direct immuno-fluorescence using a fluorescent-activated cell sorter (FACS) (FACS-calibur, BD).