喀麦隆的艾滋病毒药物耐药性和遗传多样性:对一线治疗方案的影响
Joseph Fokam1,2,3,4, Collins Ambe Chenwi1,3,5, Valère Tala1,3
1Chantal BIYA International Reference Centre for Research on HIV/AIDS Prevention and Management, Messa, Yaoundé P.O. Box 3077, Cameroon.
Viruses
|July 29, 2023
概括
喀麦隆的高艾滋病毒耐药性降低了第一线抗逆转录病毒疗法 (ART) 的有效性. 非核酸逆转录酶抑制剂耐药性普遍存在,特别是在两个地区,需要转向NRTI节省疗法.
科学领域:
- 病毒学和传染病学.
- 公共卫生和流行病学
- 抗微生物耐药性 抗微生物耐药性
背景情况:
- 一线抗逆转录病毒疗法 (ART) 的有效性可能会受到先前存在的HIV抗药性 (HIVDR) 的损害.
- 了解HIV-1治疗前耐药性 (PDR) 模式对于有效的HIV管理策略至关重要.
- 在HIVDR的区域差异可能会影响公共卫生干预和治疗指南.
研究的目的:
- 为了描述喀麦隆的HIV-1 PDR模式.
- 评估病毒基因对PDR的影响.
- 评估PDR对一线ART治疗方案的方案影响.
主要方法:
- 从2014年到2019年在喀麦隆进行的PDR的哨兵监视.
- 对HIV-1蛋白酶和逆转录酶基因的测序.
- 使用斯坦福大学HIVdb.v.9.4的HIVDR解释,分析了379个序列.
主要成果:
- 全国PDR率为15.0%,区域差异很大 (p = 0.03).
- 对非核逆转录酶抑制剂 (NNRTIs) 观察到的最高PDR为12.4%,对efavirenz/nevirapine (EFV/NVP) 耐药性为7.9%.
- 两个地区 (远北和东部) 超过了EFV/NVP PDR的10%关键值;TDF-3TC-DTG疗法与TDF-3TC-EFV (92%) 相比,显示出更高的预测效率 (98.4%).
结论:
- 喀麦隆的高PDR率,无论HIV-1遗传多样性如何,都会影响基于EFV/NVP的第一线ART的疗效.
- 特定地区显示EFV/NVP阻力处于关键水平,这带来了重大程序性挑战.
- 支持紧急过渡到节省NNRTI的ART疗法,TDF-3TC-DTG证明了最佳的程序有效性.
相关概念视频
Retrovirus Life Cycles
46.2K
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
46.2K
Treatment Resistant Cancers
3.3K
Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.3K


