Development of a Vessel-on-a-Chip as a Viral Infection Model and Antiviral Drug Screening Platform with Viral Mimics.

Publication date: Jun 29, 2025

COVID-19 pandemic and recurrent influenza outbreaks have underscored the urgent need for robust in vitro systems to model viral infections and facilitate antiviral drug screening. Using organ-on-a-chip technologies, endothelial cells were cultured to recapitulate a three-dimensional (3D) microvascular environment enhanced with higher physiologic relevance. This work aims to construct a simple yet biologically representative disease model that can be easily applied to drug screening in a high-throughput, time-efficient manner. To mimic viral infections, inflammation was induced using virus-mimicking particles, specifically polyinosinic-polycytidylic acid, while anti-inflammatory drugs RVX-208, JQ-1, and PFI-1 were evaluated for their therapeutic potential in reducing inflammation. Imaging analysis revealed that a polyinosinic-polycytidylic acid concentration of 5 μg/mL yielded the highest VCAM-1 expression, an indication of inflammation. Combining the results from VCAM-1 intensity measurements and vascular diameter changes in drug-treated cases, the effective dose of each drug was suggested. This vessel-on-a-chip platform demonstrates significant potential for advancing studies on vascular pathophysiology and antiviral treatments, offering convenient approaches for investigating both viral agents and therapeutic drugs.

Concepts Keywords
Biomater BRD4 inhibitors
Covid vasculogenesis
Easily VCAM-1
Organ vessel-on-a-chip
Virus viral mimicry

Semantics

Type Source Name
drug DRUGBANK Sulodexide
disease MESH Viral Infection
disease MESH COVID-19 pandemic
disease MESH influenza
disease MESH inflammation

Original Article

(Visited 3 times, 1 visits today)