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. 2017 Jun 5;13(6):e1006361. doi: 10.1371/journal.ppat.1006361

Table 1. Frequency of selecting HLA class I molecules in the US HIV+ population (fH).

NK cells respond to (A) mutations at PC-1 (i.e. 1 residue from the C terminus) or PC-2 in peptides presented by any HLA-C, B*46:01 or B*73:01 molecule, (B) mutations at any position except residue 2 and PC, (C) mutations at PC-1 or PC-2 of 9mers only or (D) mutations at PC-1 or PC-2 in peptides presented by HLA-C1 group molecules only. HLA molecules are considered to be ‘selecting’ if they bind a variant peptide that obeys the definitions (A-D) above, or if they do not bind the wildtype peptide but bind at least one variant peptide; the latter figure is added to give the total frequency of selecting HLAs reported in the table below (see S1 Text for example calculation).

Frequency of selecting HLAs (fH)
Protein(position) A B C D
Env(17/20) 0.77 0.77 0.04 0.47
Vpu(71/74) 0.30 0.32 0.20 0.30
Gag(138) 0.001 0.02 0 0
Nef(9) 0.37 0.51 0.02 0.35
Tat(3) 0.11 0.11 0.11 0
Vpu(3) 0.17 0.40 0.17 0.17