Division of Clinical Pharmacology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J Infect Dis. 2024 Apr 12;229(4):1131-1140. doi: 10.1093/infdis/jiad535.
Despite highly effective HIV preexposure prophylaxis (PrEP) options, no options provide on-demand, nonsystemic, behaviorally congruent PrEP that many desire. A tenofovir-medicated rectal douche before receptive anal intercourse may provide this option.
Three tenofovir rectal douches-220 mg iso-osmolar product A, 660 mg iso-osmolar product B, and 660 mg hypo-osmolar product C-were studied in 21 HIV-negative men who have sex with men. We sampled blood and colorectal tissue to assess safety, acceptability, pharmacokinetics, and pharmacodynamics.
The douches had high acceptability without toxicity. Median plasma tenofovir peak concentrations for all products were several-fold below trough concentrations associated with oral tenofovir disoproxil fumarate (TDF). Median colon tissue mucosal mononuclear cell (MMC) tenofovir-diphosphate concentrations exceeded target concentrations from 1 hour through 3 to 7 days after dosing. For 6-7 days after a single product C dose, MMC tenofovir-diphosphate exceeded concentrations expected with steady-state oral TDF 300 mg on-demand 2-1-1 dosing. Compared to predrug baseline, HIV replication after ex vivo colon tissue HIV challenge demonstrated a concentration-response relationship with 1.9 log10 maximal effect.
All 3 tenofovir douches achieved tissue tenofovir-diphosphate concentrations and colorectal antiviral effect exceeding oral TDF and with lower systemic tenofovir. Tenofovir douches may provide a single-dose, on-demand, behaviorally congruent PrEP option, and warrant continued development. Clinical Trials Registration . NCT02750540.
尽管有高效的 HIV 暴露前预防(PrEP)选择,但没有一种选择提供按需、非系统性、行为一致的 PrEP,而这是许多人所期望的。在接受肛门性交前使用含有替诺福韦的直肠冲洗剂可能提供这种选择。
我们在 21 名男男性行为者中研究了三种含有替诺福韦的直肠冲洗剂-220mg 等渗产品 A、660mg 等渗产品 B 和 660mg 低渗产品 C。我们采集了血液和结直肠组织样本,以评估安全性、可接受性、药代动力学和药效学。
这些冲洗剂具有很高的接受度,没有毒性。所有产品的血浆替诺福韦峰浓度均远低于与口服替诺福韦二吡呋酯(TDF)相关的谷浓度。中位结肠组织粘膜单核细胞(MMC)替诺福韦二磷酸浓度在给药后 1 小时至 3 至 7 天内超过目标浓度。在单次使用产品 C 后 6-7 天内,MMC 替诺福韦二磷酸浓度超过了按需口服 TDF 300mg 2-1-1 给药的稳态浓度。与给药前基线相比,离体结肠组织 HIV 挑战后 HIV 复制显示出与 1.9 log10 最大效应浓度相关的浓度反应关系。
三种替诺福韦直肠冲洗剂均达到了组织替诺福韦二磷酸浓度和结直肠抗病毒效果,超过了口服 TDF,且全身替诺福韦浓度较低。替诺福韦直肠冲洗剂可能提供一种单剂量、按需、行为一致的 PrEP 选择,值得进一步开发。临床试验注册. NCT02750540。