Academic Journal

Electrochemotherapy impacts the viability, functionality and phenotype of murine dendritic cells in voltage-dependent manner

Bibliographic Details
Title: Electrochemotherapy impacts the viability, functionality and phenotype of murine dendritic cells in voltage-dependent manner
Authors: Bendix, Maura B, Baker, Kevin J, Forde, Patrick F, Houston, Aileen, Brint, Elizabeth
Publisher Information: Elsevier
Publication Year: 2026
Collection: University College Cork, Ireland: Cork Open Research Archive (CORA)
Subject Terms: Animals, Dendritic Cells/cytology, Cell Survival/drug effects, Mice, Electrochemotherapy/methods, Inbred C57BL, Toll-Like Receptors/metabolism, Phenotype, Cytokines/metabolism, [Medicine]
Description: Dendritic cells (DCs) are central to the initiation of anti-tumour immunity, yet the direct effects of electrochemotherapy (ECT) on DC biology remain poorly defined. We investigated how varying electric field strengths (800, 1000, and 1300 V/cm) modulate murine DC viability, phenotype, Toll-like receptor (TLR) expression and functional responses in vitro. ECT induced predominantly necrotic cell death in a voltage-dependent manner, with higher voltages markedly reducing viability. Despite this decline, surviving DCs exposed to 1000 V/cm and 1300 V/cm upregulated MHC II and CD80, indicating activation of the remaining population. ECT also altered TLR expression, significantly increasing TLR6 and TLR9 while reducing TLR4, TLR7 and TLR8 levels. Functionally, ECT impaired DC cytokine responses to TLR4 and TLR7/8 stimulation but preserved or enhanced responsiveness to the TLR9 agonist CpG, suggesting selective disruption of downstream TLR pathways. Together, these findings demonstrate that ECT differentially shapes DC survival and function depending on electric field intensity, with low-voltage ECT better preserving DC competence and higher voltages inducing activation but impairing responsiveness. These data highlight opportunities to optimise ECT protocols and rationally combine ECT with immune adjuvants to enhance therapeutic immunogenicity.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: 109263; Baker, Kevin J; Forde, Patrick F; Bioelectrochemistry; https://hdl.handle.net/10468/18682; 170
DOI: 10.1016/j.bioelechem.2026.109263
Availability: https://hdl.handle.net/10468/18682
https://doi.org/10.1016/j.bioelechem.2026.109263
Rights: © 2026, the authors. Published by Elsevier B.V. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/ ). ; https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.71317947
Database: BASE
Description
DOI:10.1016/j.bioelechem.2026.109263