Viral Tropism and Antiretroviral Drug Resistance in HIV-1 Subtype C-Infected Patients Failing Highly Active Antiretroviral Therapy in Johannesburg, South Africa

被引:0
|
作者
Ketseoglou, Irene [1 ,2 ]
Lukhwareni, Azwidowi [2 ]
Steegen, Kim [1 ]
Carmona, Sergio [1 ,2 ]
Stevens, Wendy S. [1 ,2 ]
Papathanasopoulos, Maria A. [1 ]
机构
[1] Univ Witwatersrand, Sch Med, Fac Hlth Sci, ZA-2193 Johannesburg, South Africa
[2] Natl Hlth Lab Serv, Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
CORECEPTOR USAGE; DISEASE PROGRESSION; CELL DEPLETION; CCR5; PHENOTYPE; LENGTH; ENTRY;
D O I
10.1089/aid.2013.0267
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Reports show that up to 30% of antiretroviral drug-naive patients in Johannesburg have CXCR4-utilizing HIV-1 subtype C. We assessed whether HIV-1 subtype C-infected individuals failing highly active antiretroviral therapy (HAART) have a higher proportion of CXCR4-utilizing viruses compared to antiretroviral drug-naive patients. The V3 loop was sequenced from plasma from 100 randomly selected HAART-failing patients, and tropism was established using predictive algorithms. All patients harbored HIV-1 subtype C with at least one antiretroviral drug resistance mutation. Viral tropism prediction in individuals failing HAART revealed similar proportions (29%) of X4-utilizing viruses compared to antiretroviral drug-naive patients (30%). Findings are in contrast to reports from Durban in which 60% of HAART-failing subjects harbored X4/dual/mixed-tropic viruses. Despite differences in proportions of X4-tropism within South Africa, the high proportion of thymidine analogue mutations (TAMs) and CXCR4-utilizing HIV-1 highlights the need for intensified monitoring of HAART patients and the predicament of diminishing drug options, including CCR5 antagonists, for patients failing therapy.
引用
收藏
页码:289 / 293
页数:5
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