Skip to main content
. 2009 Nov;117(11):849–855. doi: 10.1111/j.1600-0463.2009.02544.x

Table 1.

Immunogenicity of seven HIV-1-derived HLA-A*0201-binding synthetic peptides

Epitope Sequence Rank1 IC50 (nM) Specific lysis (%)2 SFU/mio splenocytes3 IFN-γ+TNF-α+4
Gag150mod RLLNAWVKV 1 26 66 ± 1.2 19657 ± 1774 16.6
Gag433 FLGKIWPS 2 3 49 ± 2.7 5714 ± 575 12.6
Vif23(9V) SLVKHHMYV 3 168 46 ± 3.6 4217 ± 146 5.0
Pol606mod KLGKAGYVV 4 384 36 ± 3.7 4391 ± 370 3.2
Env67(2I) NIWATHACV 5 103 28 ± 0.8 3658 ± 223 3.6
Vif101(9L) GLADQLIHL 6 219 17 ± 0.9 nd 2.5
Vpu66mod ALVEMGHHV 7 334 No lysis nd 2.2

Values represent data from groups of four mice with pooled splenocytes. HIV-1; human immunodeficiency virus type 1; HLA, human leukocyte antigen; SFU, spot-forming unit; IFN-γ, γ-interferon; TNF-α, tumor necrosis factor-α; nd, not determined.

1

Epitopes are ranked according to decreasing immunogenicity.

2

Mean values at effector target ratio 50:1, ± indicate SD of triplicates.

3

Mean values, ± indicate SD of triplicates.

4

Values represent percentage double-positive IFN-γ and TNF-α-producing CD3+CD8+ T cells from pooled splenocytes (n = 4 mice) in order to obtain sufficient cell counts for optimal analysis.