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. 2002 Sep 6;99(19):12275–12280. doi: 10.1073/pnas.182418399

Table 1.

Immunogenicity of selected hTRT HLA A2.1-binding peptides

Peptide Sequence Relative avidity Immunogenicity
p152 LLARCALFV 15
pY152 YLARCALFV 5 50, 36, 14, 0, 88, 16, 36, 83
p407 VLLKTHCLP 10
pY407 YLLKTHCLP 10 0, 0, 0, 0
p555 ELLRSFFYV 35
pY555 YLLRSFFYV 3 72, 46, 12, 0, 21, 18, 27, 97
p572 RLFFYRKSV 30
pY572 YLFFYRKSV 1.9 45, 24, 9, 44, 92, 21, 73
p675 LLGASVLGL >30
pY675 YLGASVLGL 2 17, 12, 0, 0
p724 RLYEVIASI >30
pY724 YLYEVIASI 3.5 6, 0, 0, 0
p1072 WLCHQAFLL >30
pY1072 YLCHQAFLL 4 17, 0, 0, 0
p540 ILAKFLHWL 2.9
p865 RLVDDFLLV 2.5
*

The denomination of peptides denotes the position of the first residue in the predicted amino acid sequence of hTRT (8).

The relative avidity is measured in arbitrary units as described in Materials and Methods.

Data represent the percent (%) specific lysis by primary CTL cultures generated from individual HHD mice immunized with the indicated analogue peptide. Values refer to % lysis of RMAS-HHD cells pulsed with the counterpart wild-type peptide (10−6 M) minus the % lysis of RMAS-HHD cells pulsed with the HLA A2-binding 58GILGFVFTL66 peptide of Influenza virus matrix antigen used as control at an E/T ratio of 50:1. Nonspecific lysis on target cells pulsed with the irrelevant peptide was between 0 and 13%.

§

p540 and p865 representing previously described high-affinity hTRT peptide (9) are shown by comparison.