Dykes Carrie, Najjar Joe, Bosch Ronald J, Wantman Michael, Furtado Manohar, Hart Stephen, Hammer Scott M, Demeter Lisa M
University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA.
J Infect Dis. 2004 Mar 15;189(6):1091-6. doi: 10.1086/382033. Epub 2004 Mar 1.
We evaluated zidovudine-experienced patients for whom treatment with indinavir, lamivudine, and zidovudine failed, for indinavir-resistant minority variants. Of 10 patients with plasma human immunodeficiency virus type 1 RNA suppression and subsequent rebound, 6 without primary indinavir-resistance mutations underwent clonal analysis. One had evidence of V82A in 9 of 30 clones at week 24, with no increase at week 40. The dominant week-40 82V-M184V clones had changes at protease codons 62-64, compared with all clones at week 24 and minority clones at week 40. Resistance to indinavir can emerge during treatment failure in nucleoside-experienced patients but may be missed by routine sequence analysis. Selection for indinavir-resistant variants on treatment with indinavir, lamivudine, and zidovudine may occur slowly, depending on the genetic context in which they arise.
我们评估了曾接受齐多夫定治疗、但使用茚地那韦、拉米夫定和齐多夫定治疗失败的患者,以检测是否存在茚地那韦耐药的少数变异株。在10例血浆中人类免疫缺陷病毒1型RNA先被抑制随后又反弹的患者中,对6例无原发性茚地那韦耐药突变的患者进行了克隆分析。其中1例在第24周时,30个克隆中有9个出现V82A,在第40周时未增加。与第24周的所有克隆以及第40周的少数克隆相比,第40周占主导地位的82V-M184V克隆在蛋白酶密码子62-64处有变化。在核苷类药物治疗失败的患者中,治疗期间可能会出现对茚地那韦的耐药,但常规序列分析可能会遗漏。使用茚地那韦、拉米夫定和齐多夫定治疗时,对茚地那韦耐药变异株的选择可能会缓慢发生,这取决于它们出现时的基因背景。