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. 2012 Mar 15;61(10):1769–1779. doi: 10.1007/s00262-012-1239-z

Table 2.

PRAME-stimulated PBMC react with L-1236 HL cells

Primary stimulation Stimulatory cells in ELISPOT Donor 1 Donor 2 Donor 3 Donor 4 Donor 5
None None 0 0 0 24
None T2 26 31 27 34
None T2-SLY (PRAME) 46 66 26 33
None L-1236 80 31 16 38
T2 None 0 0 24
T2 T2 0 36 110
T2 T2-SLY (PRAME) 0 119
T2 L-1236 0 22 137
T2-SLY None 39 0 23 222 60
T2-SLY T2 288 344 278 290
T2-SLY T2-LDY (LIPI) 150
T2-SLY T2-SLY (PRAME) 283 538 390 362 160
T2-SLY L-1236 190 294 237 295 107
T2-ALY None 46
T2-ALY T2-LDY (LIPI) 190
T2-ALY T2-ALY (PRAME) 248
T2-ALY L-1236 246
T2-VLD None 62
T2-VLD T2-LDY (LIPI) 222
T2-VLD T2-VLD (PRAME) 203
T2-VLD L-1236 215

HLA-A2-positive PBMC were primed with T2 cells or with T2 cells that had been pulsed with 100 μg/ml of PRAME-derived peptides SLY, ALY and VLD, respectively (primary stimulation). Reactivity of stimulated cells with T2 cells and L-1236 cells was assessed by interferon gamma ELISPOT. For this end, T2 cells had been pulsed with PRAME-derived peptides (T2-SLY, T2-ALY and T2-VLD), peptides derived by the irrelevant antigen LIPI (T2-LDY) or left un-pulsed (T2). Presented are means from triplicates after background subtraction. – not done

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