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. Author manuscript; available in PMC: 2016 Apr 1.
Published in final edited form as: J Immunol. 2015 Feb 20;194(7):3487–3500. doi: 10.4049/jimmunol.1401717

Table III.

Specific recognition of HLA-A2+ MART1+ tumor cells by Jurkat 76/CD8αβ reconstituted with A2/MART1 TCRs

TRBV27 chain
Stimulator cells HLA-A2 MART1 Cl.413 Cl.523 Cl.788 Cl.1086 Cl.758 Cl.1593 Cl.1574 Cl.1599 Cl.1606 Cl.830 Cl.794 DMF5
A375 + <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10
A375/MART1 + + <10 <10 21 (6) 20 (5) 45 (7) 98 (8) 55 (9) 170 (3) 94 (10) 153 (8) 197 (10) 33 (3)
Malme-3M/siControl + + <10 <10 18 (5) 19 (8) 64 (6) 73 (15) 60 (11) 143 (18) 76 (10) 99 (8) 151 (15) 39 (5)
Malme-3M/siMART1 + Low <10 <10 14 (5) 14 (6) 50 (6) 54 (5) 45 (9) 99 (10) 48 (4) 75 (9) 113 (11) 27 (5)
SK-MEL-28 + <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10
SK-MEL-28/A2 + + <10 <10 34 (6) 31 (4) 67 (9) 101 (14) 81 (4) 128 (14) 70 (6) 115 (10) 147 (10) 40 (6)
SK-MEL-37 + <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10
K562 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10 <10

Tumor cell recognition was assessed using various target cells, which did or did not express HLA-A2 and/or MART1, as stimulator cells in IL-2 ELISPOT assays. A half million Jurkat 76/CD8αβ cells, which were individually transduced with eleven distinct clonotypic TRBV27 TCRβ chains along with SIG35α or with DMF5αβ chains, were used as responder cells. Mean values of SFUs in triplicate samples are shown. SDs of triplicates are shown in parentheses.

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