Eicher Barbara, Esslinger Christoph, Hillenbrand Matthias
Memo Therapeutics AG, Schlieren, Switzerland.
Front Pharmacol. 2025 Apr 25;16:1572739. doi: 10.3389/fphar.2025.1572739. eCollection 2025.
This study investigates the biodistribution of a therapeutic antibody from serum to urine across the kidney endothelial barrier, contextualizing the findings with existing literature. Our analysis shows the quantitative correlation between serum levels of the intravenously administered antibody rituximab and its urinary concentration, indicating a predictable pharmacokinetic profile. The results align with previous quantitative studies on the biodistribution of endogenous and vaccination induced IgG between serum and urine, confirming that recombinant therapeutic IgG1 passes the kidney endothelial barrier and exhibits similar biodistribution to endogenous IgG. These insights may inform the determination of optimal dosages for therapeutic antibodies targeting the urothelium or renal epithelium.
本研究调查了一种治疗性抗体从血清到尿液穿过肾内皮屏障的生物分布情况,并结合现有文献对研究结果进行解读。我们的分析显示,静脉注射抗体利妥昔单抗的血清水平与其尿液浓度之间存在定量相关性,表明其具有可预测的药代动力学特征。这些结果与先前关于内源性和疫苗诱导的IgG在血清和尿液之间生物分布的定量研究一致,证实重组治疗性IgG1可穿过肾内皮屏障,并表现出与内源性IgG相似的生物分布。这些见解可能有助于确定针对尿路上皮或肾上皮的治疗性抗体的最佳剂量。