Blood was collected in sodium heparin tubes and processed within 3 h of collection. The whole blood assay was adapted from the protocol described by Hanekom et al.46 (link) Briefly, 0.5 ml of whole blood was stimulated with a pool of 300 Mtb-derived peptides (Mtb300, 2 µg/ml)47 (link) at 37 °C for 5 h in the presence of the costimulatory antibodies, anti-CD28 and anti-CD49d (1 μg/ml each; BD Biosciences) and Brefeldin-A (10 µg/ml; Sigma-Aldrich). Unstimulated cells were incubated with costimulatory antibodies and Brefeldin-A only. Red blood cells were then lysed in a 150 mM NH4Cl, 10 mM KHCO3, and 1 mM Na4EDTA solution. Cells were stained with a Live/Dead Near-InfraRed dye (Invitrogen), and then fixed using a Transcription Factor Fixation buffer (eBioscience), cryopreserved in freezing media (50% fetal bovine serum, 40% RPMI, and 10% dimethyl sulfoxide) and stored in liquid nitrogen until use.
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