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. 2000 Sep 26;97(20):10948–10953. doi: 10.1073/pnas.97.20.10948

Table 1.

Summary of resistance mutations selected during successful therapy

Pt. Previous drugs* Current drugs* Baseline mutations Clone no. New mutations (Clone no.)
Analyzed by molecular cloning
 M ZDV ZDV + 3TC + IDV RT 41L, 44D, 67N, 70R, 215Y 42 RT 118I (3)
 C ZDV ZDV + 3TC + IDV RT 67N, 70R, 219Q 98 PR 54V; RT 184V (2)
 K ddI, ZDV ZDV + 3TC + IDV PR {71V}; RT 41L, 74V, 215Y 39 PR 46I, 77I; RT 118I, 210W (2)
 L ZDV ZDV + 3TC + IDV RT 67N, 219Q 26 PR 46V, I;RT 69D, 70R (6)
 A ZDV ZDV + 3TC + IDV RT 70R 17 None
 B ZDV ZDV + 3TC + IDV RT 70R 36 None
Analyzed by biological cloning
 9 RTV, RTV + ZDV DV + 3TC + RTV + SQ Gag (p7p1)V; PR 54V, 77I, 82A; RT 70R (on-HAART) 65 (6 times) PR {10I, 71V}, 90M (6)
 11 None d4T + RTV + SQV 4 None
 23 None ZDV + 3TC + IDV 16 None
 24 None ZDV + 3TC + NFV 12 None
*

ZDV, zidovudine; 3TC, lamivudine; IDV, indinavir; RTV, ritonavir; SQV, saquinavir; d4T, stavudine; and NFV, nelfinavir. 

Baseline resistance mutations were identified in ref. 1. New on-therapy resistance mutations selected by drugs given only during the current successful regimen are in bold: lamivudine selected (italics and bold) and protease inhibitor selected (bold, not italicized). Brackets signify natural polymorphisms, which may also be drug-selected. Each position was not interrogated in every clone.