“…[1][2][3] It was extracted with phosphate-buffered saline [(PBS, pH 7.5), 1Ϻ5 wt/vol] at 4°C for 1 hour followed by centrifugation at 5,000 rpm. The supernatants were passed through the syringe filter (MIS, USA: 0.25-m pore sized), dialyzed (cut-off molecular weight of 6,000 D) against 4 L of distilled water at 4°C for 48 hours, and lyophilized at Ϫ70°C to prepare the antigens to be used for stimulation of epithelial cells.…”