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. 2005 Nov 10;107(6):2294–2302. doi: 10.1182/blood-2005-08-3503

Table 2.

Identification of multiple pentadecapeptides eliciting HSV-TK-specific CD8+ CTL responses after HyTK-positive DLI

% IFN+ CD8+ T cells
Patient (HLA type) and immunogenic 15-mer sequence*(no. of peptide) % in T-cell line % in PBMCs
UPN 1574 (A3, A24, B7, B35)
    RRTALRPRRQQEATE25-39 (11) 3.4 0.15 (1.2)
    VPEPMTYWRVLGASE81-95 (25) 3.1 0.17 (1.3)
    QITMGMPYAVTDAVL125-139 (36) 3.8 0.17 (0.9)
    FDRHPIAALLCYPAA161-175 (45) 5.9 0.30 (2.8)
    NAGPRPHIGDTLFTL277-291 (74) 10.6 0.29 (0.4)
    YDQSPAGCRDALLQL329-343 (87) 7.8 0.20 (1.2)
UPN 4103 (A1, A24, B8, B27)
    GHSNRRTALRPRRQQ21-35 (10) 8.8 0.54
    LLCYPAARYLMGSMT169-183 (47) 7.2 0.31
    HIDRLAKRQRPGERL213-227 (58) 1.1 0.27
    LAMLAAIRRVYGLLA229-243 (62) 1.7 0.34
    PQGAEPQSNAGPRPH269-283 (72) 1.2 0.48
UPN 7826 (A1, A3, B44, B57)
    PIAALLCYPAARYLM165-179 (46) 61.4 0.15
*

Position within the sequence of the 376 aa HSV-TK protein (GenBank accession nos. V000467, CAA23741).

T-cell lines were generated by stimulating samples of postinfusion PBMCs obtained from each of the 3 patients with γ-irradiated donor T cells expressing HyTK (UPN 1574, UPN 4103) or HSV-TK (UPN 7826).

IFN-γ+ CD8+ T cells in PBMCs (days 14 to 28) after the first HyTK-positive T-cell infusion. For UPN 1574, the frequency of IFN-γ-producing T cells to each epitope 28 days after infusion 2 is shown in parentheses.