Impact of Human Immunodeficiency Virus Type-1 Sequence Diversity on Antiretroviral Therapy Outcomes

被引:16
作者
Langs-Barlow, Allison [1 ]
Paintsil, Elijah [2 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Child Hlth Res Ctr, Dept Pediat, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Child Hlth Res Ctr, Dept Pharmacol, New Haven, CT 06520 USA
来源
VIRUSES-BASEL | 2014年 / 6卷 / 10期
关键词
human immunodeficiency virus; subtypes; polymorphisms; mutations; drug resistance; antiretroviral therapy; TREATMENT-NAIVE PATIENTS; DRUG-RESISTANCE MUTATIONS; NON-B SUBTYPES; REVERSE-TRANSCRIPTASE INHIBITORS; HIGH-LEVEL RESISTANCE; HIV TYPE-1; VIROLOGICAL FAILURE; IN-VITRO; MINORITY POPULATIONS; REPLICATIVE FITNESS;
D O I
10.3390/v6103855
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Worldwide circulating HIV-1 genomes show extensive variation represented by different subtypes, polymorphisms and drug-resistant strains. Reports on the impact of sequence variation on antiretroviral therapy (ART) outcomes are mixed. In this review, we summarize relevant published data from both resource-rich and resource-limited countries in the last 10 years on the impact of HIV-1 sequence diversity on treatment outcomes. The prevalence of transmission of drug resistant mutations (DRMs) varies considerably, ranging from 0% to 27% worldwide. Factors such as geographic location, access and availability to ART, duration since inception of treatment programs, quality of care, risk-taking behaviors, mode of transmission, and viral subtype all dictate the prevalence in a particular geographical region. Although HIV-1 subtype may not be a good predictor of treatment outcome, review of emerging evidence supports the fact that HIV-1 genome sequence-resulting from natural polymorphisms or drug-associated mutations-matters when it comes to treatment outcomes. Therefore, continued surveillance of drug resistant variants in both treatment-naive and treatment-experienced populations is needed to reduce the transmission of DRMs and to optimize the efficacy of the current ART armamentarium.
引用
收藏
页码:3855 / 3872
页数:18
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