Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, 98109, USA.
Department of Global Health, University of Washington, Seattle, WA, 98196, USA.
Nat Commun. 2023 Nov 28;14(1):7813. doi: 10.1038/s41467-023-43399-5.
Broadly neutralizing monoclonal antibodies (mAbs) are being developed for HIV-1 prevention. Hence, these mAbs and licensed oral pre-exposure prophylaxis (PrEP) (tenofovir-emtricitabine) can be concomitantly administered in clinical trials. In 48 US participants (men and transgender persons who have sex with men) who received the HIV-1 mAb VRC01 and remained HIV-free in an antibody-mediated-prevention trial (ClinicalTrials.gov #NCT02716675), we conduct a post-hoc analysis and find that VRC01 clearance is 0.08 L/day faster (p = 0.005), and dose-normalized area-under-the-curve of VRC01 serum concentration over-time is 0.29 day/mL lower (p < 0.001) in PrEP users (n = 24) vs. non-PrEP users (n = 24). Consequently, PrEP users are predicted to have 14% lower VRC01 neutralization-mediated prevention efficacy against circulating HIV-1 strains. VRC01 clearance is positively associated (r = 0.33, p = 0.03) with levels of serum intestinal Fatty Acid Binding protein (I-FABP), a marker of epithelial intestinal permeability, which is elevated upon starting PrEP (p = 0.04) and after months of self-reported use (p = 0.001). These findings have implications for the evaluation of future HIV-1 mAbs and postulate a potential mechanism for mAb clearance in the context of PrEP.
广谱中和单克隆抗体(mAbs)正在被开发用于 HIV-1 的预防。因此,这些 mAbs 和已许可的口服暴露前预防(PrEP)(替诺福韦-恩曲他滨)可在临床试验中同时使用。在接受 HIV-1 mAb VRC01 的 48 名美国参与者(男性和跨性别者与男性发生性关系)中,他们在一项抗体介导的预防试验中保持了 HIV 阴性(ClinicalTrials.gov #NCT02716675),我们进行了一项事后分析,发现 VRC01 的清除速度快了 0.08 L/天(p = 0.005),并且在 PrEP 使用者(n = 24)中,VRC01 血清浓度的时间曲线下面积与剂量归一化比非 PrEP 使用者(n = 24)低 0.29 天/mL(p < 0.001)。因此,PrEP 使用者的 VRC01 中和介导的预防效果预计会降低 14%,以抵御循环中的 HIV-1 株。VRC01 的清除与血清肠脂肪酸结合蛋白(I-FABP)水平呈正相关(r = 0.33,p = 0.03),I-FABP 是上皮肠通透性的标志物,在开始使用 PrEP 时(p = 0.04)和几个月的自我报告使用后(p = 0.001)升高。这些发现对未来 HIV-1 mAbs 的评估具有影响,并提出了 PrEP 背景下 mAb 清除的潜在机制。