Division of Digestive Diseases, Department of Internal Medicine, University of Cincinnati College of Medicine, ML 0595, 231 Albert Sabin Way, Cincinnati, OH, 45267-0595, USA.
Addiction Sciences Division, Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
J Neurovirol. 2022 Dec;28(4-6):583-594. doi: 10.1007/s13365-022-01090-3. Epub 2022 Aug 17.
The US is experiencing a major public health crisis that is fueled by the illicit use of synthetic opioids including fentanyl. While several drugs of abuse can enhance viral replication and/or antagonize immune responses, the impact of specific synthetic opioids on HIV pathogenesis is poorly understood. Thus, we evaluated the effects of fentanyl on HIV replication in vitro. HIV-susceptible or HIV-expressing cell lines were incubated with fentanyl. HIV p24 synthesis and chemokine receptor levels were quantified by ELISA in culture supernatants and cell lysates, respectively. Addition of fentanyl resulted in a dose-dependent increase in HIV replication. Fentanyl enhanced expression of the HIV chemokine co-receptors CXCR4 and CCR5 and caused a dose-dependent decrease in cell viability. The opioid antagonist naltrexone blocked the effect of fentanyl on HIV replication and CCR5 receptor levels but not CXCR4 receptor levels. TLR9 expression was induced by HIV; however, fentanyl inhibited TLR9 expression in a dose-dependent manner. These data demonstrate that the synthetic opioid fentanyl can promote HIV replication in vitro. As increased HIV levels are associated with accelerated disease progression and higher likelihood of transmission, additional research is required to enhance the understanding of opioid-virus interactions and to develop new and/or optimized treatment strategies for persons with HIV and opioid use disorder.
美国正经历一场重大的公共卫生危机,这场危机是由包括芬太尼在内的合成阿片类药物的非法使用所助长的。虽然几种滥用药物可以增强病毒复制和/或拮抗免疫反应,但特定的合成阿片类药物对 HIV 发病机制的影响还不太清楚。因此,我们评估了芬太尼对 HIV 在体外复制的影响。将 HIV 易感或 HIV 表达细胞系与芬太尼孵育。通过 ELISA 分别在培养上清液和细胞裂解物中定量测定 HIV p24 合成和趋化因子受体水平。芬太尼的加入导致 HIV 复制呈剂量依赖性增加。芬太尼增强了 HIV 趋化因子共受体 CXCR4 和 CCR5 的表达,并导致细胞活力呈剂量依赖性下降。阿片受体拮抗剂纳曲酮阻断了芬太尼对 HIV 复制和 CCR5 受体水平的影响,但对 CXCR4 受体水平没有影响。HIV 诱导 TLR9 的表达;然而,芬太尼以剂量依赖性方式抑制 TLR9 的表达。这些数据表明,合成阿片类药物芬太尼可以促进 HIV 在体外复制。由于 HIV 水平的升高与疾病进展加速和传播可能性增加有关,因此需要进一步研究,以增强对阿片类药物-病毒相互作用的理解,并为 HIV 和阿片类药物使用障碍患者开发新的和/或优化的治疗策略。