CD40-activated B cells can be prepared at relatively low costs as a highly pure homogenous population that can be expanded from small check details amount of peripheral blood even from cancer patients [28]. However, it is not known whether tumor-derived immunosuppressive factors affect the antigen-presenting capacity of CD40-activated B cells in a similar fashion as in DC. We therefore studied the effect of IL-10, TGF-β, Selleckchem CB-839 and VEGF on the phenotype, migratory ability, and T cell stimulatory capacity of CD40-activated B cells in vitro. Methods Flow cytometry Immunophenotypic analysis was performed

using fluorescence-activated cell sorting (FACS) according to standard protocols. The cells were analyzed on a FACSCanto flow cytometer (BD Biosciences, Heidelberg, Germany). Antibodies against CD19, CD80, CD86, HLA-DR, CD3, and CD25 were purchased from BD Pharmingen (Heidelberg, Germany). Generation of CD40-activated B cells and AG-120 order cell culture CD40-B cells were generated as described previously [29]. In brief, whole PBMC were cultured on

irradiated NIH3T3 fibroblasts transfected with human CD40 ligand (tCD40L) in the presence of recombinant human interleukin-4 (2 ng/ml; R&D Systems, Minneapolis, MN, USA) and clinical-grade cyclosporin A (CsA, 5·5 × 10−7 M; Novartis, Basel, Switzerland) in Iscove’s modified Dulbecco’s medium (IMEM; Invitrogen, Karlsruhe, Germany) supplemented with 10% pooled human serum. The expanding cells were transferred onto freshly prepared tCD40L cells and fed with cytokine-replenished medium without CsA every 3–4 days. After 2–3 weeks in culture the CD40-activated B cells had a purity of >95 % and were used for the experiments. Therefore they were cultured

for 4 days in the presence of 40 ng/ml IL-10, 10 ng/ml TGF-β, 20 ng/ml VEGF or vehicle as a control. For Ibrutinib molecular weight these concentrations the inhibitory effects on APC functions of DCs have been demonstrated previously [11]. Prior to use the activity of IL-10, TGF-β, and VEGF at the given concentrations was tested by assessing their inhibitory effect on DC maturation and for IL-10 and TGF-β additionally on T cell proliferation. In vitro migration assay To assess B cell migration, 5 × 105 CD40-B cells were transferred into the upper chamber of 5-μm pore size transwell plates (Costar, Cambridge, MA, USA). Varying amounts of the chemokines SDF-1α and SLC (R&D Systems) were added to the lower chamber. After 2 hours at 37°C, the number of cells that had migrated into the lower chamber was determined using a hemacytometer. T cell proliferation assay Untouched CD4+ T cells and CD8+ T cells were obtained from buffy coats by negative selection using Rosette Sep® (StemCell Technologies) human CD4+ and CD8+ T cell enrichment cocktails according manufacturers’ instructions.