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作者信息

Bangoura Nestor, Diouara Abou A M, Cissé Mohamed, Ndiaye Halimatou D, Mboup Souleymame, Ayouba Ahidjo, Kane Coumba T

机构信息

Service de Dermatologie CHU Donka, CTA, Conakry, Guinée.

Laboratoire de Bactériologie Virologie CHU Aristide Le Dantec, Université Cheikh Anta Diop de Dakar, Sénégal.

出版信息

Afr J Lab Med. 2015 Jun 26;4(1):168. doi: 10.4102/ajlm.v4i1.168. eCollection 2015.

Abstract

UNLABELLED

Quantification of Viral load and resistance tests of HIV-1 to ARVs from dried blood spots samples in Guinean patients undergoing antiretroviral treatment.

PROBLEM

As in several countries of the South, the virological monitoring of patients undergoing antiretroviral treatment (ARVT) in Guinea is low or non-existent in some locations. The aim of this study was to assess the technical and logistical feasibility of the use of (dried blood spots) DBSs in viral load (VL) and genotyping tests.

METHOD

From September 2010 to October 2010, DBS were prepared from blood samples of adult patients under ARVT. The samples had to be sent to the reference laboratory within 30 days after the sample had been done at ambient temperature. The VL was quantified and the samples of patients with virological failure (CV ≥ 3 log copies/mL) were genotyped according to the ANRS protocol. The Stanford algorithm, version 6.0.8, was used to analyse and interpret the resistance mutations.

RESULTS

Amongst the 136 included patients, 129 and 7 were under first and second line treatment respectively, and monitored for an average of 35 months [IQR: 6-108]. Virological failure was noticed among 33 patients. Among them, 84.8% ( = 28/33) benefited from genotyping. The global resistance rate was 14% ( = 19/136). CRF02_AG was the most prevalent viral subtype (82%; = 23).

CONCLUSION

In addition to demonstrating the technical and logistic feasibility of VL and genotyping tests from DBSs, these results show the relevance of their use in the virological monitoring of patients under ARVT. Also, this study made it possible to provide information on virological failure, ARV resistance and the HIV-1 genetic diversity in Guinea.

摘要

未标注

对几内亚接受抗逆转录病毒治疗的患者干血斑样本进行HIV-1病毒载量定量及对抗逆转录病毒药物的耐药性检测。

问题

与其他一些南方国家一样,几内亚接受抗逆转录病毒治疗(ARVT)患者的病毒学监测在某些地区水平较低或根本不存在。本研究的目的是评估使用干血斑(DBS)进行病毒载量(VL)和基因分型检测的技术和后勤可行性。

方法

2010年9月至2010年10月,从接受ARVT的成年患者血液样本中制备干血斑。样本在室温下采集后必须在30天内送至参考实验室。根据法国国家艾滋病研究机构(ANRS)方案对病毒载量进行定量,并对病毒学失败(CV≥3 log拷贝/毫升)患者的样本进行基因分型。使用斯坦福算法6.0.8版分析和解释耐药突变。

结果

在纳入的136例患者中,129例和7例分别接受一线和二线治疗,平均监测35个月[四分位间距:6 - 108]。33例患者出现病毒学失败。其中,84.8%(=28/33)接受了基因分型。总体耐药率为14%(=19/136)。CRF02_AG是最常见的病毒亚型(82%;=23)。

结论

这些结果除了证明通过干血斑进行病毒载量和基因分型检测的技术和后勤可行性外,还表明了其在接受ARVT患者病毒学监测中的相关性。此外,本研究能够提供有关几内亚病毒学失败、抗逆转录病毒药物耐药性和HIV-1基因多样性的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/10911652/251e2ee3fb18/AJLM-4-168-g001.jpg

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