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. 2009 Sep 2;83(22):11514–11527. doi: 10.1128/JVI.01298-09

TABLE 1.

Mamu-B*08-restricted CD8+ T-cell epitopes mutated in 8X-SIVmac239a

Epitope Amino acid sequenceb Mamu-B*08 binding affinity (IC50 [nM])c Fold reduction in binding to Mamu-B*08
Vif172-179RL8 RRDNRRGL 125
.G...... 594 4.8d
Vif123-131RL9 RRAIRGEQL 7.5
.K....... 2,901 387d
Nef137-146RL10 (A)RRHRILDIYL 11
(P).......... NT NAe
Nef246-254RL9b RRLTARGLL 3.2
........P 477 151d
Env573-581KL9 KRQQELLRL 12
........M 397 33d
Rev12-20KL9 KRLRLIHLL 3.2
.....L... 1.6 Nonef
Nef8-16RL9a RRSRPSGDL 105
....Q.... 428 4.1g
Rev44-51RL8 RRRWQQLL 20
......I. 59 2.9f
a

Epitopes are listed in order of the typical immunodominance hierarchy of responses targeting the epitopes. Subscript numbers in the epitope name indicate amino acid positions of the epitope.

b

The mutations introduced are indicated beneath the sequence of the epitope. These changes are indicated in boldface type.

c

Peptides with IC50s of >500 nM are not considered binders and are indicated in italics. The binding of WT and 8X variant peptides to Mamu-B*08 was described previously (33). NT, not tested.

d

The putative mechanism of escape is a primary anchor residue mutation.

e

The putative mechanism of escape is a processing mutation. NA, not applicable, as the mutation introduced is outside the defined epitope.

f

The putative mechanism of escape is a TCR contact mutation.

g

The putative mechanism of escape is TCR contact mutation along with some reduction in Mamu-B*08 binding.