Combinatorial treatment of Birinapant and Zosuquidar enhances effective control of HBV replication In vivo
Details
Publication Year 2020-08-17,Volume 12,Issue #8,Page 901
Journal Title
Viruses
Publication Type
Journal Article
Abstract
Chronic hepatitis B virus (HBV) infection remains a global health threat and affects hundreds of millions worldwide. Small molecule compounds that mimic natural antagonists of inhibitor of apoptosis (IAP) proteins, known as Smac-mimetics (second mitochondria-derived activator of caspases-mimetics), can promote the death of HBV-replicating liver cells and promote clearance of infection in preclinical models of HBV infection. The Smac-mimetic birinapant is a substrate of the multidrug resistance protein 1 (MDR1) efflux pump, and therefore inhibitors of MDR1 increase intracellular concentration of birinapant in MDR1 expressing cells. Liver cells are known to express MDR1 and other drug pump proteins. In this study, we investigated whether combining the clinical drugs, birinapant and the MDR1 inhibitor zosuquidar, increases the efficacy of birinapant in killing HBV expressing liver cells. We showed that this combination treatment is well tolerated and, compared to birinapant single agent, was more efficient at inducing death of HBV-positive liver cells and improving HBV-DNA and HBV surface antigen (HBsAg) control kinetics in an immunocompetent mouse model of HBV infection. Thus, this study identifies a novel and safe combinatorial treatment strategy to potentiate substantial reduction of HBV replication using an IAP antagonist.
Publisher
MDPI
Research Division(s)
Inflammation; Infectious Diseases And Immune Defence
PubMed ID
32824616
Open Access at Publisher's Site
https://doi.org/10.3390/v12080901
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2020-10-17 02:40:35
Last Modified: 2020-11-03 10:09:37
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