Capacity limits of asialoglycoprotein receptor-mediated liver targeting.
Charlotte BonThomas HoferAlain Bousquet-MélouMark R DaviesBen-Fillippo KrippendorffPublished in: mAbs (2017)
The abundant cell surface asialoglycoprotein receptor (ASGPR) is a highly selective receptor found on hepatocytes that potentially can be exploited as a selective shuttle for delivery. Various nucleic acid therapeutics that bind ASGPR are already in clinical development, but this receptor-mediated delivery mechanism can be saturated, which will likely result in reduced selectivity for the liver and therefore increase the likelihood for systemic adverse effects. Therefore, when aiming to utilize this mechanism, it is important to optimize both the administration protocol and the molecular properties. We here present a study using a novel ASGPR-targeted antibody to estimate ASGPR expression, turnover and internalization rates in vivo in mice. Using pharmacokinetic data (intravenous and subcutaneous dosing) and an in-silico target-mediated drug disposition (TMDD) model, we estimate an ASGPR expression level of 1.8 million molecules per hepatocyte. The half-life of the degradation of the receptor was found to be equal to 15 hours and the formed ligand-receptor complex is internalized with a half-life of 5 days. A biodistribution study was performed and confirmed the accuracy of the TMDD model predictions. The kinetics of the ASGPR shows that saturation of the shuttle at therapeutic concentrations is possible; however, simulation allows the dosing schedule to be optimized. The developed TMDD model can be used to support the development of therapies that use the ASGPR as a shuttle into hepatocytes.
Keyphrases
- poor prognosis
- nucleic acid
- randomized controlled trial
- cell surface
- liver injury
- cancer therapy
- drug induced
- emergency department
- small molecule
- type diabetes
- high dose
- bone mineral density
- metabolic syndrome
- electronic health record
- postmenopausal women
- low dose
- deep learning
- insulin resistance
- data analysis
- pet imaging