Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269, USA.
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269, USA; Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.
Biochem Pharmacol. 2018 Dec;158:298-304. doi: 10.1016/j.bcp.2018.10.035. Epub 2018 Nov 2.
Phosphoantigens stimulate Vγ9Vδ2 T cells after binding to BTN3A1 in target cells and cell-cell contact. We evaluated phosphoantigens including diphosphates, bisphosphonates, and prodrugs for ability to induce leukemia cells to stimulate Vγ9Vδ2 T cell interferon-γ secretion. Most compounds displayed time-dependent activity at exposure times between 15 and 240 min. Potency (EC values) ranged between 8.4 nM and >100 µM. The diphosphate C-HMBPP displayed a shallow dose-response slope (Hill slope = 0.71), while the bisphosphonate slopes were steep (Hill slopes > 2), and the prodrugs intermediate. The bis-acyloxyalkyl POM-C-HMBP showed low nanomolar potency even at an exposure time of 1 min. Mixed aryl-POM prodrugs also retained excellent potency at 15 min, while aryl-amidates were time dependent below 240 min. The sum of the dose and time logarithms is often constant, while a power law function fits most compounds. Collectively, these findings illustrate the exquisite activity of prodrugs relative to diphosphates and bisphosphonates.
磷酸抗原与靶细胞中的 BTN3A1 结合并通过细胞间接触后可刺激 Vγ9Vδ2 T 细胞。我们评估了包括二磷酸盐、双膦酸盐和前药在内的磷酸抗原诱导白血病细胞刺激 Vγ9Vδ2 T 细胞干扰素-γ分泌的能力。大多数化合物在 15 至 240 分钟的暴露时间内显示出时间依赖性活性。效力(EC 值)范围在 8.4 nM 至 >100 µM 之间。二磷酸盐 C-HMBPP 显示出平缓的剂量反应斜率(Hill 斜率= 0.71),而双膦酸盐的斜率较陡(Hill 斜率> 2),前药则处于中间位置。即使在 1 分钟的暴露时间下,双-烷氧基烷基 POM-C-HMBP 也表现出低纳摩尔效力。混合芳基-POM 前药在 15 分钟时仍保持优异的效力,而芳基酰胺则在 240 分钟以下呈时间依赖性。剂量和时间对数的总和通常是恒定的,而幂函数适合大多数化合物。总的来说,这些发现说明了前药相对于二磷酸盐和双膦酸盐具有极高的活性。