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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.
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页码:289 / 293
页数:5
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