2010
DOI: 10.1111/j.1468-1293.2009.00747.x
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Prevalence of drug resistance and importance of viral load measurements in Honduran HIV‐infected patients failing antiretroviral treatment

Abstract: ObjectiveThe Honduran HIV/AIDS Program began to scale up access to HIV therapy in 2002. Up to May 2008, more than 6000 patients received combination antiretroviral therapy (cART). As HIV drug resistance is the major obstacle for effective treatment, the purpose of this study was to assess the prevalence of antiretroviral drug resistance in Honduran HIV-1-infected individuals. MethodsWe collected samples from 138 individuals (97 adults and 41 children) on cART with virological, immunological or clinical signs o… Show more

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Cited by 36 publications
(33 citation statements)
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“…34,35 TDR was identified using the WHO 2009 list of mutations for surveillance of TDR as implemented in the Calibrated Population Resistance tool (v4.2 beta; hivdb.stanford.edu). 36 The susceptibility of the viruses to antiretroviral drugs was predicted using the ANRS algorithm (version 2008/07; http://hivfrenchresistance.org).…”
Section: Genotypic Resistance Analysismentioning
confidence: 99%
“…34,35 TDR was identified using the WHO 2009 list of mutations for surveillance of TDR as implemented in the Calibrated Population Resistance tool (v4.2 beta; hivdb.stanford.edu). 36 The susceptibility of the viruses to antiretroviral drugs was predicted using the ANRS algorithm (version 2008/07; http://hivfrenchresistance.org).…”
Section: Genotypic Resistance Analysismentioning
confidence: 99%
“…Five (0.8%) sequences were classified as subtype C, and two (0.3%) sequences had previously been identified as unique recombinant forms (URFs), URF_AD and URF_AK (21). Table 1 lists the baseline characteristics of the 632 patients.…”
Section: Hiv-1 Subtype Classificationmentioning
confidence: 99%
“…Sequence analysis of the protease (PR) and the first part of the reverse transcriptase (RT) of the HIV-1 pol gene (nucleotides 2268 to 3257 of reference strain HXB2, PR nucleotides 16 to 297, and RT nucleotides 1 to 708) was performed on the plasma or serum samples by using a published protocol (21,22,24). Dried-blood-spot samples were sequenced using another published genotyping assay developed by the CDC (25,26).…”
mentioning
confidence: 99%
“…For the PCR and sequencing reactions primers were used as reported elsewhere, spanning the entire protease gene and 1-253 amino acids of the reverse transcriptase gene. 9 Amplicons were purified with the addition of enzymes Exonuclease I and Shrimp Alkaline Phosphatase (Thermo Fisher Scientific, Waltham, MA) and subjected to direct sequencing using a BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems) with four primers giving bidirectional sequences. A DyeEx 2.0 Spin Kit (Qiagen) was used according to the manufacturer's instructions for the removal of unincorporated dye terminators from the sequencing reactions and obtained sequences were assembled using Vector NTI Advance v 11.0 (Invitrogen, Carlsbad, CA).…”
mentioning
confidence: 99%