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Intrapatient Evolutionary Dynamics of Human Immunodeficiency Virus Type 1 in Individuals Undergoing Alternative Treatment Strategies with Reverse Transcriptase Inhibitors
被引:0
作者:
Kayondo, Jonathan K.
[1
]
Ndembi, Nicaise
[2
]
Parry, Chris M.
[2
]
Cane, Patricia A.
[3
]
Hue, Stephane
[4
]
Goodall, Ruth
[5
]
Dunn, David T.
[5
]
Kaleebu, Pontiano
[1
,2
]
Pillay, Deenan
[4
]
Mbisa, Jean L.
[3
]
机构:
[1] Uganda Virus Res Inst, Uganda Res Unit AIDS, Entebbe, Uganda
[2] UVRI, MRC, Uganda Res Unit AIDS, Entebbe, Uganda
[3] Publ Hlth England, Virus Reference Dept, London, England
[4] UCL, Dept Infect & Immun, London, England
[5] UCL, MRC, Clin Trials Unit, London, England
基金:
英国惠康基金;
关键词:
DRUG-RESISTANCE;
HIV;
INTERRUPTION;
INFECTION;
D O I:
10.1089/aid.2015.0035
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Structured treatment interruption (STI) has been trialed as an alternative to lifelong antiretroviral therapy (ART). We retrospectively performed single genome sequencing of the HIV-1 pol region from three patients representing different scenarios. They were either failing on continuous therapy (CT-F), failing STI (STI-F), or suppressing on STI (STI-S). Over 460 genomes were generated from three to five different time points over a 2-year period. We found multiple-linked-resistant mutations in both treatment failures. However, the CT-F patient showed a stepwise accumulation of diverse, linked mutations whereas the STI-F patient had lineage turnover between treatment periods with recirculation of wild-type and resistant variants from reservoirs. The STI-F patient showed a 7-fold increase in the third codon position substitution rate relative to the first and second positions compared to a 2-fold increase for CT-F and increased purifying selection in the pol gene (62 vs. 22 sites, respectively). An understanding of intrapatient viral dynamics could guide the future direction of treatment interruption strategies.
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页码:749 / 756
页数:8
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