Whether CD8+CD39+ T cells are

associated with IL-17 responses and/or protection needs further investigation. In this article, we describe for the first time a functional role for CD39 on human BCG-activated CD8+CD39+ Treg cells. We show that CD39 expression marks a CD8+ Treg-cell subset, which co-expresses LAG-3, CD25, Foxp3, and CCL4, and that CD39 may play a direct role in exerting CD8+ Treg-dependent suppression. CD8+CD39+ Treg cells represent a new player in balancing immunity and inflammation in host defense against mycobacteria, and possibly contribute to (lack of) vaccine-mediated protection. Anonymous buffy coats were collected from healthy learn more adult blood bank donors that had signed consent for scientific use of blood products. PBMCs were isolated by density centrifugation and cryopreserved in fetal calf serum supplemented medium. Cells were counted using the CASY cell counter (Roche, Woerden, The Netherlands). Recognition of mycobacterial PPD was tested by assessing IFN-γ production in vitro. PBMCs were LDE225 mw stimulated with 5 μg/mL PPD (Statens Serum Institute, Copenhagen, Denmark) for 6 days and supernatants were tested in IFN-γ ELISA (U-CyTech, Utrecht, The Netherlands).

Positivity was defined as IFN-γ production ≥150 pg/mL. PBMCs were cultured in Iscove’s modified Dulbecco’s medium (Life Technologies-Invitrogen, Bleiswijk, The

Netherlands) supplemented with 10% pooled human serum. BCG (Pasteur) was grown in 7H9 plus ADC, frozen in 25% glycerol and stored at –80°C. Before use, bacteria were thawed and washed in PBS/0.05% Tween 80 (Sigma-Aldrich, Zwijndrecht, The Netherlands). Infections were done at an MOI of 1.5. IL-2 (25U/mL; Proleukin; Novartis Pharmaceuticals UK Ltd., Horsham, UK) was added Phosphoribosylglycinamide formyltransferase after 6 days of culture. Restimulation of cell lines was done in 96-well round-bottom plates (1 × 105 cells/w) with αCD3/CD28 beads (Dynabeads Human T-activator, Life Technologies-Invitrogen), IL-2 (50 U/mL), IL-7, and IL-15 (both 5 ng/mL, Peprotech, Rocky Hill, NJ, USA); pooled, irradiated (30 Gy) PBMCs were added as feeders. Cells were maintained in IL-2 (100 U/mL). T-cell lines were incubated overnight with αCD3/28 beads, for the last 16 h Brefeldin A (3 μg/mL, Sigma-Aldrich) was added. Following the labeling with the violet live/dead stain (VIVID, Invitrogen), the following antibodies were used for surface staining: CD3-PE-Texas Red, CD14- and CD19-Pacific Blue (all Invitrogen), CD4-PeCy7, CD8-HorizonV500, CD73-PerCPCy5.5 (all BD Biosciences, Eerembodegem, Belgium), and CD39-PE (Biolegend, London, UK).