Department of Molecular Medicine and Haematology, University of the Witwatersrand, Johannesburg, South Africa.
J Acquir Immune Defic Syndr. 2010 Apr 1;53(4):480-4. doi: 10.1097/QAI.0b013e3181bc478b.
The South African national antiretroviral therapy roll-out program is entering its sixth year, with over 570,000 adults accessing treatment. HIV-1 drug resistance is a potential consequence of therapy. This study determined the pattern of HIV-1 drug resistance mutations after failure of first-line treatment regimens in South Africa.
Two hundred and twenty-six patients virologically failing first-line regimens were studied to determine resistance patterns.
The most common reverse transcriptase mutation was M184V/I (72%; n = 163); 11% of patients (n = 25) had only nonnucleoside reverse transcriptase inhibitor (NNRTI) mutations and 17% (n = 38) had no known resistance mutations. The K65R mutation was detected in 4%. The frequency of thymidine analog mutations was significantly higher with azidothymidine-containing (31 of 57) than stavudine-containing regimens (39 of 169; P < 0.001). The Y181C mutation was more frequent with failure of nevirapine (NVP)-containing (26%) than efavirenz (EFV)-containing therapy (3%; P < 0.001). The V106M mutation was more frequent with EFV (30%) than NVP (4%; P = 0.012).
HIV-1 drug resistance patterns varied broadly after failure of first-line therapy, ranging from no known resistance mutations (17%) to multinucleoside reverse transcriptase inhibitor and NNRTI resistance (23%). NNRTI mutation profiles differed for patients on EFV- compared with NVP-containing regimens. Overall, these findings suggest that HIV-1 drug resistance testing would be useful in identifying most appropriate second-line regimens.
南非国家抗逆转录病毒治疗推出计划已进入第六个年头,已有超过 57 万名成年人接受治疗。HIV-1 耐药性是治疗的潜在后果。本研究旨在确定南非一线治疗方案失败后 HIV-1 耐药突变的模式。
对 226 名病毒学上一线治疗方案失败的患者进行研究,以确定耐药模式。
最常见的逆转录酶突变是 M184V/I(72%;n=163);11%的患者(n=25)仅有非核苷类逆转录酶抑制剂(NNRTI)突变,17%(n=38)没有已知的耐药突变。检测到 4%的 K65R 突变。含叠氮胸苷的方案(31/57)中胸苷类似物突变的频率明显高于含司他夫定的方案(39/169;P<0.001)。奈韦拉平(NVP)方案失败时,Y181C 突变更常见(26%),而依非韦伦(EFV)方案失败时则更少见(3%;P<0.001)。EFV 方案失败时 V106M 突变更常见(30%),NVP 方案失败时则更少见(4%;P=0.012)。
一线治疗失败后,HIV-1 耐药模式广泛,从无已知耐药突变(17%)到多种核苷逆转录酶抑制剂和 NNRTI 耐药(23%)不等。EFV 方案和 NVP 方案的 NNRTI 突变谱不同。总的来说,这些发现表明 HIV-1 耐药性检测将有助于确定最合适的二线治疗方案。