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印度西部资源有限环境下免疫监测后的抗逆转录病毒耐药性:一项横断面研究。

Antiretroviral resistance following immunological monitoring in a resource-limited setting of western India: A cross-sectional study.

作者信息

Karade Santosh K, Kulkarni Smita S, Ghate Manisha V, Patil Ajit A, Londhe Rajkumar, Salvi Sonali P, Kadam Dileep B, Joshi Rajneesh K, Rewari Bharat B, Gangakhedkar Raman R

机构信息

HIV Drug Resistance Laboratory, National AIDS Research Institute (ICMR), Pune, India.

Department of Microbiology, Armed Forces Medical College, Pune, India.

出版信息

PLoS One. 2017 Aug 1;12(8):e0181889. doi: 10.1371/journal.pone.0181889. eCollection 2017.

Abstract

BACKGROUND

The free antiretroviral therapy (ART) program in India still relies on the clinico-immunological monitoring for diagnosis of treatment failure. As the nucleoside reverse transcriptase inhibitor (NRTI) backbone is shared in first- and second-line regimens, accumulation of drug resistant mutations (DRMs) can compromise the efficacy of NRTI. This study was undertaken to describe the pattern of HIV DRMs following immunological monitoring and investigate its impact on the cycling of NRTI between first- and second-line ART.

METHODS AND FINDINGS

This cross-sectional study was performed at a state-sponsored ART clinic of Pune city in western India between January and June 2016. Consecutive adults receiving first-line ART with immunological failure (IF) were recruited for plasma viral load (PVL) estimation. Randomly selected 80 participants with PVL >1000 copies/mL underwent HIV drug resistance genotyping. Of these, 75 plasma sample were successfully genotyped. The median CD4 count and duration of ART at the time of failure were 98 (IQR: 61.60-153.50) cells/μL and 4.62 (IQR: 3.17-6.15) years, respectively. The prevalence of NRTI, non-NRTI, and major protease inhibitor resistance mutations were 89.30%, 96%, and 1.33%, respectively. Following first-line failure, sequences from 56.67% of individuals indicated low- to high-level resistance to all available NRTI. The proportion of sequences with ≥2 thymidine analogue mutations (TAMs) and ≥3 TAMs were 62.12% and 39.39%, respectively. An average of 1.98 TAMs per sequence were observed following IF as compared to 0.37 TAMs per sequence following targeted PVL monitoring at 12 months of ART from a prior study; this difference was significant (p<0.001).

CONCLUSION

The option of cycling of NRTI analogues between first- and second-line regimens would no longer be effective if individuals are followed-up by immunological monitoring due to accumulation of mutations. Introduction of routine PVL monitoring is a priority for the long-term sustainability of free ART program in India.

摘要

背景

印度的免费抗逆转录病毒疗法(ART)项目仍依赖临床免疫学监测来诊断治疗失败情况。由于一线和二线治疗方案中都使用核苷类逆转录酶抑制剂(NRTI)作为主干药物,耐药突变(DRM)的积累可能会影响NRTI的疗效。本研究旨在描述免疫监测后HIV耐药突变的模式,并调查其对一线和二线ART中NRTI循环使用的影响。

方法与结果

本横断面研究于2016年1月至6月在印度西部浦那市一家由政府资助的ART诊所进行。招募连续接受一线ART且出现免疫失败(IF)的成年患者进行血浆病毒载量(PVL)评估。随机选择80名PVL>1000拷贝/mL的参与者进行HIV耐药基因分型。其中,75份血浆样本成功进行了基因分型。失败时的CD4计数中位数和ART疗程分别为98(四分位间距:61.60 - 153.50)个细胞/μL和4.62(四分位间距:3.17 - 6.15)年。NRTI、非NRTI和主要蛋白酶抑制剂耐药突变的发生率分别为89.30%、96%和1.33%。一线治疗失败后,56.67%的个体序列显示对所有可用NRTI存在低水平至高水平耐药。具有≥2个胸苷类似物突变(TAM)和≥3个TAM的序列比例分别为62.12%和39.39%。IF后每条序列平均观察到1.98个TAM,而先前一项研究中在ART 12个月时进行靶向PVL监测后每条序列平均为0.37个TAM;这种差异具有统计学意义(p<0.001)。

结论

如果通过免疫监测对个体进行随访,由于突变积累,在一线和二线治疗方案之间循环使用NRTI类似物的选择将不再有效。引入常规PVL监测是印度免费ART项目长期可持续性的优先事项。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/5538665/a6e82ddacb36/pone.0181889.g001.jpg

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