To increase the purity, the positively selected cell fraction containing the CD4+CD25+CD127dim/− regulatory T cells was separated over a second, new column. Depletion of non-CD4+ and CD127high cells was performed on an LD Column. The subsequent positive selection of CD4+CD25+CD127dim/− T cells was performed on two MS Columns. The purity of Treg separation was always greater

Seliciclib cell line than 90% as assessed in flow cytometer with monoclonal antibodies (CD4, CD25 and CD127). RNA extraction and cDNA synthesis.  Total RNA from T regulatory cells (CD4+CD25+CD127dim/−) was isolated and purified using Rneasy Mini Kit (Qiagen, Valencia, CA, USA) following the manufacturer’s protocol. RNA integrity was verified by 1.5% agarose gel electrophoresis/ethidium bromide staining and OD260/280 absorption ratio >1.95. One microgram of total RNA was used to prepare cDNA. cDNA synthesis was performed using SuperScript™ First-Strand Synthesis System for RT-PCR (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions in the MJ Research Thermal Cycler (MJ Research, Model PTC-200; Watertown, MA, USA). Real-Time PCR.  The following

genes were assessed: (1) cytokines and H 89 solubility dmso chemokines: IL-2, IL-10 (and its receptor α), TGF-β1 (and its receptors 1 and 2), IL-12A, IL-17A, IL-21, IL-23, IL-27, EBI3, IL-8 receptor α, CCL22, interferon (IFN)-γ, tumour necrosis factor (TNF)-α; (2) critical Treg molecules: OX40, 4-1BB, ICOS, GITR, CTLA-4, perforin-1, granzyme A and (3) transcription factors: FoxP3, STAT1, STAT3, SOCS2, SOCS3, SMAD3 and T-box 21. The levels of transcripts were measured by real-time PCR using human genes QuantiTect Hs_IL7R_1_SG

Assay (Qiagen) and QuantiTect Hs_GAPDH Assay (Qiagen) as a normalizer. Real-Time PCR was performed in duplicate in 20 μl using mafosfamide the QuantiTect SYBR Green PCR Master Mix (Qiagen) following the manufacturer’s instructions and carried out in the Chromo4 Real-Time PCR Detector (BIO-RAD, Hercules, CA, USA). The thermal cycling conditions included an initial activation step at 95 °C for 15 min, followed by 40 cycles of denaturation, annealing and amplification (94 °C for 15 s, 55 °C for 30 s, 72 °C for 30 s). At the end of the amplification phase, a melting curve analysis was carried out on the product formed. The fluorescent data collection was performed during the annealing step. A standard curve construction was generated by using a serial of four dilutions of cDNA of the control group sample in reaction with the house-keeping gene, GAPDH. Based on these curves, the levels of total chosen gene transcripts were calculated after its normalization to GAPDH. The value of CT was determined by the first cycle number at which fluorescence was greater than the set threshold value. To calculate our data, according to Livak and Schmittgen [15], we used the comparative CT method for relative quantification i.e. 2−ΔΔCT method. Statistical analysis.