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. Author manuscript; available in PMC: 2012 Mar 27.
Published in final edited form as: J Immunol. 2010 May 7;184(11):6514–6521. doi: 10.4049/jimmunol.0900448

Table II.

Identified MART-126-35 APLs exhibit differential capacities to generate MART-126-35-specific CTL populations from the PBMC of different melanoma patient donors.

%M26 Tetramer Positive
Patient A27L E26G E26S L33M
MelPt-A 3.14 (1) 1.68 (0.53) 3.36 (1.07) 0.98 (0.31)
MelPt-B 2.97 (1) 1.31 (0.44) 4.3 (1.45) 7.7 (2.6)
MelPt-C 40.6 (1) 45.6 (1.12) 15.6 (0.38) 41.1 (1.02)
MelPt-D 0.65 (1) 1.73 (2.66) 3.43 (5.27) 2.07 (3.1)
MelPt-E 1.77 (1) 8.42 (4.75) 6.88 (3.88) 24.2 (13.67)
MelPt-F 5.45 (1) 3.35 (0.61) 3.72 (0.68) 3.07 (0.56)
MelPt-G 33.4 (1) 1.89 (.06) 1.75 (.05) 2.37 (.07)
MelPt-H 1.24 (1) 2.03 (1.63) 1.31 (1.06) 2.77 (2.2)

APLs were used to stimulate PBMC cultures in vitro. Following a 1-week secondary stimulation cells were stained with FITC-labeled anti-CD8 antibodies and APC-labeled HLA-A2/ MART-126-35 tetramers and analyzed by flow cytometry. Percent tetramer positive indicated. Fold difference relative to A27L is indicated in parentheses. Differences of more than two-fold are indicated in bold.