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. Author manuscript; available in PMC: 2008 Oct 6.
Published in final edited form as: J Immunother. 1997 Jul;20(4):276–286. doi: 10.1097/00002371-199707000-00004

TABLE 2.

Specific reactivity of virally induced anti-MART-1 cytotoxic T lymphocytes (CTL) against various HLA-A*0201 compatible MART-1-derived peptides and naturally processed MART-1 epitopes on tumor cells

T2 + MART-1 peptide
Effector 27–35 31–39 32–40 35–43 56–64 T2 + G9-209-2M 624.38-Mel 624.28-Mel
CTL-1 1,724 0 0 0 54 34 815 0
CTL-2 666 184 204 195 160 156 209 60
CTL-3 683 64 49 56 124 93 137 35
CTL-4 438 91 99 114 7 0 58 0
CTL-5 3,924 392 396 424 404 340 1,416 147
CTL-6 844 392 356 344 348 376 44 0
A42 anti-MART-1 27-35 clone >4,000 0 54 0 0 0 2,559 13
1235 TIL >4,000 5 155 0 53 12 3,704 30
Anti-G9 209-2M CTL 0 0 0 0 0 >4,000 1,154 0

CTL 1–6 were raised by stimulation with dendritic cells (DC) infected with rV-MART-1 and restimulated after 7 days with DC infected with rF-MART-1. Interferon-γ release (pg/5 × 105 CD8 cells/24 h) was analyzed against T2 cells pulsed with peptide (2 μg/ml) or against the HLA-A*0201+/MART-1 + 624.38 MEL or the HLA-A*0201 –/MART-1 + 624.28 MEL melanoma clones (37). As effector controls, anti-MART-127-35 A42 CTL clone and 1235 tumor-infiltrating lymphocytes and anti-G9-209-2M CTL were used.