Jespersen Sanne, Tolstrup Martin, Hønge Bo Langhoff, Medina Candida, Té David da Silva, Ellermann-Eriksen Svend, Østergaard Lars, Wejse Christian, Laursen Alex Lund
Bandim Health Project, Indepth Network, Apartado 861, Bissau, Guinea-Bissau.
Department of Infectious Diseases, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, 8200, Aarhus N, Denmark.
Virol J. 2015 Mar 11;12:41. doi: 10.1186/s12985-015-0273-9.
With the widespread use of antiretroviral treatment (ART) in Africa, the risk of drug resistance has increased. The aim of this study was to evaluate levels of HIV-1 resistance among patients with HIV-1 and HIV-1/2 dual infections, treated with ART, at a large HIV clinic in Guinea-Bissau.
Patients were selected from the Bissau HIV cohort. All patients had HIV-1 or HIV-1/2 dual infection, a CD4 cell count performed before and 3-12 months after starting ART, and a corresponding available plasma sample. We measured viral load in patients with HIV-1 (n = 63) and HIV-1/2 dual (n = 16) infections a median of 184 days after starting ART (IQR: 126-235 days). In patients with virological failure (defined as viral load >1000 copies/ml) and with sufficient plasma available, we performed an HIV-1 genotypic resistance test. Thirty-six patients (46%) had virological failure. The CD4 cell count did not predict treatment failure. Of the 36 patients with virological failure, we performed a resistance test in 15 patients (42%), and nine patients (9/15; 60%) had resistance mutations. The most common mutation was K103N, which confers high-level resistance to non-nucleoside reverse transcriptase inhibitors (NNRTI). No major mutations against protease inhibitors (PI) were found.
Our results showed that patients with HIV-1 and HIV-1/2 dual infections in Guinea-Bissau had a high rate of virological failure and rapid development of NNRTI resistance. It remains to be determined whether a more robust, PI-based treatment regimen might benefit this population more than NNRTIs.
随着抗逆转录病毒治疗(ART)在非洲的广泛应用,耐药风险有所增加。本研究的目的是评估在几内亚比绍一家大型艾滋病诊所接受ART治疗的HIV-1感染者及HIV-1/2双重感染者中HIV-1的耐药水平。
患者选自比绍艾滋病队列。所有患者均为HIV-1感染或HIV-1/2双重感染,在开始ART治疗前及治疗3至12个月后进行了CD4细胞计数,并采集了相应的血浆样本。我们在开始ART治疗中位数184天(四分位间距:126 - 235天)后测量了HIV-1感染者(n = 63)及HIV-1/2双重感染者(n = 16)的病毒载量。对于病毒学失败(定义为病毒载量>1000拷贝/ml)且有足够血浆样本的患者,我们进行了HIV-1基因型耐药检测。36名患者(46%)出现病毒学失败。CD4细胞计数不能预测治疗失败。在36名病毒学失败的患者中,15名患者(42%)进行了耐药检测,其中9名患者(9/15;60%)有耐药突变。最常见的突变是K103N,它赋予对非核苷类逆转录酶抑制剂(NNRTI)的高水平耐药。未发现针对蛋白酶抑制剂(PI)的主要突变。
我们的结果表明,几内亚比绍的HIV-1感染者及HIV-1/2双重感染者病毒学失败率高,且NNRTI耐药发展迅速。基于PI的更强化治疗方案对比NNRTIs是否能使该人群更多获益仍有待确定。