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. 2006 Jan 4;347(1):127–139. doi: 10.1016/j.virol.2005.11.042

Table 1.

T-cell IFN-γ ELISpot positive N-peptide sequences

N peptides
IFN-γ SFC/106 splenocytes (mean ± SD)
Number N-aa Sequence p-hLAMP-N p-N N-GST
11 76–93 NTNSGPDDQIGYYRRATR 57 ± 2 3 ± 2 6 ± 1
12 80–99 GPDDQIGYYRRATRRVRGGD 429 ± 8 266 ± 18 46 ± 12
13 84–101 QIGYYRRATRRVRGGDGK 377 ± 11 209 ± 6 55 ± 6
14 92–109 TRRVRGGDGKMKELSPRW 309 ± 13 212 ± 7 24 ± 5
15 100–114 GKMKELSPRWYFYYL 75 ± 12 55 ± 7 9 ± 2
21 130–149 GIVWVATEGALNTPKDHIGT 106 ± 4 61 ± 8 5 ± 3
35 241–258 QQQGQTVTKKSAAEASKK 131 ± 20 23 ± 3 2 ± 1
51 352–366 ILLNKHIDAYKTFPP 137 ± 10 34 ± 8 38 ± 4
52 353–370 LLNKHIDAYKTFPPTEPK 118 ± 11 50 ± 8 46 ± 11

All ELISpot responses were to a group of 9 dominant peptides, shown by peptide number, amino acid region in N, sequence, and number of IFN-γ-positive cells of mice immunized with the three immunogens. A cluster (N76–114) of 5 peptides of 15 to 20 aa, overlapping by 10 to 16, contains 3 of the strongest dominant epitopes.