de Mendoza Carmen, Paxinos Ellen, Barreiro Pablo, Camino Nuria, Núñez Marina, Soriano Vincent
Service of Infectious Diseases, Hospital Carlos III, Madrid, Spain.
J Clin Microbiol. 2004 Feb;42(2):862-6. doi: 10.1128/JCM.42.2.862-866.2004.
A total of 76 patients discontinued treatment with didanosine plus hydroxyurea after 1 year of maintenance therapy. The greatest human immunodeficiency virus (HIV)-RNA rebounds were seen in 10 patients harboring an L74V mutation, and the presence of viruses with this mutation rapidly waned. In contrast, viral rebounds were significantly less pronounced (P < 0.01) in 12 subjects harboring thymidine-associated mutations; these mutations persisted in all instances. Thus, selection of an L74V mutation during didanosine therapy may compromise HIV replication in vivo.
共有76例患者在接受1年维持治疗后停止使用去羟肌苷加羟基脲治疗。在10例携带L74V突变的患者中观察到最大的人类免疫缺陷病毒(HIV)-RNA反弹,且携带该突变的病毒迅速减少。相比之下,12例携带胸苷相关突变的受试者的病毒反弹明显不那么明显(P<0.01);这些突变在所有情况下均持续存在。因此,在去羟肌苷治疗期间选择L74V突变可能会损害体内HIV的复制。