pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus

Oncolytic viruses have emerged as a promising modality in cancer treatment given their high synergy with highly efficient immune checkpoint inhibitors. However, their potency is limited by their rapid in vivo clearance. To overcome this, we coated oncolytic vaccinia viruses (oVV) with erythrocyte-de...

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發表在:Pharmaceutics
Main Authors: Kaelan T. Samoranos, Alexandra L. Krisiewicz, Bianca C. Karpinecz, Philip A. Glover, Trevor V. Gale, Carla Chehadeh, Sheikh Ashshan, Richard Koya, Eddie Y. Chung, Han L. Lim
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語言:英语
出版: MDPI AG 2022-08-01
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在線閱讀:https://www.mdpi.com/1999-4923/14/9/1810
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author Kaelan T. Samoranos
Alexandra L. Krisiewicz
Bianca C. Karpinecz
Philip A. Glover
Trevor V. Gale
Carla Chehadeh
Sheikh Ashshan
Richard Koya
Eddie Y. Chung
Han L. Lim
author_facet Kaelan T. Samoranos
Alexandra L. Krisiewicz
Bianca C. Karpinecz
Philip A. Glover
Trevor V. Gale
Carla Chehadeh
Sheikh Ashshan
Richard Koya
Eddie Y. Chung
Han L. Lim
author_sort Kaelan T. Samoranos
collection DOAJ
container_title Pharmaceutics
description Oncolytic viruses have emerged as a promising modality in cancer treatment given their high synergy with highly efficient immune checkpoint inhibitors. However, their potency is limited by their rapid in vivo clearance. To overcome this, we coated oncolytic vaccinia viruses (oVV) with erythrocyte-derived membranes (EDMs), hypothesizing that they would not only remain in systemic circulation for longer as erythrocytes would when administered intravenously, but also respond to environmental pH cues due to their membrane surface sialic acid residues. For this, we developed a model based on DLVO theory to show that the acidic moieties on the surface of EDM confers it the ability to respond to pH-based stimuli. We corroborate our modeling results through in vitro cell culture models and show that EDM-coated oVV infects cancer cells faster under acidic conditions akin to the tumor microenvironment. When EDM-coated oVVs were intravenously injected into wild-type mice, they exhibited prolonged circulation at higher concentrations when compared to the unprocessed oVV. Furthermore, when EDM-coated oVV was directly injected into xenografted tumors, we observed that they were suppressed earlier than the tumors that received regular oVV, suggesting that the EDM coating does not hinder oVV infectivity. Overall, we found that EDM was able to serve as a multi-functional encapsulant that allowed the payload to remain in circulation at higher concentrations when administered intravenously while simultaneously exhibiting pH-responsive properties.
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spelling doaj-art-cf18ae26a66d40fea2da5c7cfffee80d2025-08-19T22:56:21ZengMDPI AGPharmaceutics1999-49232022-08-01149181010.3390/pharmaceutics14091810pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia VirusKaelan T. Samoranos0Alexandra L. Krisiewicz1Bianca C. Karpinecz2Philip A. Glover3Trevor V. Gale4Carla Chehadeh5Sheikh Ashshan6Richard Koya7Eddie Y. Chung8Han L. Lim9Coastar Therapeutics Inc., San Diego, CA 92121, USACoastar Therapeutics Inc., San Diego, CA 92121, USACoastar Therapeutics Inc., San Diego, CA 92121, USANeon Insights Consulting, Auburndale, MA 02466, USACoastar Therapeutics Inc., San Diego, CA 92121, USACoastar Therapeutics Inc., San Diego, CA 92121, USACoastar Therapeutics Inc., San Diego, CA 92121, USADepartment of Obstetrics and Gynecology, Pritzker School of Medicine, The University of Chicago, Chicago, IL 60637, USACoastar Therapeutics Inc., San Diego, CA 92121, USACoastar Therapeutics Inc., San Diego, CA 92121, USAOncolytic viruses have emerged as a promising modality in cancer treatment given their high synergy with highly efficient immune checkpoint inhibitors. However, their potency is limited by their rapid in vivo clearance. To overcome this, we coated oncolytic vaccinia viruses (oVV) with erythrocyte-derived membranes (EDMs), hypothesizing that they would not only remain in systemic circulation for longer as erythrocytes would when administered intravenously, but also respond to environmental pH cues due to their membrane surface sialic acid residues. For this, we developed a model based on DLVO theory to show that the acidic moieties on the surface of EDM confers it the ability to respond to pH-based stimuli. We corroborate our modeling results through in vitro cell culture models and show that EDM-coated oVV infects cancer cells faster under acidic conditions akin to the tumor microenvironment. When EDM-coated oVVs were intravenously injected into wild-type mice, they exhibited prolonged circulation at higher concentrations when compared to the unprocessed oVV. Furthermore, when EDM-coated oVV was directly injected into xenografted tumors, we observed that they were suppressed earlier than the tumors that received regular oVV, suggesting that the EDM coating does not hinder oVV infectivity. Overall, we found that EDM was able to serve as a multi-functional encapsulant that allowed the payload to remain in circulation at higher concentrations when administered intravenously while simultaneously exhibiting pH-responsive properties.https://www.mdpi.com/1999-4923/14/9/1810cancerpH responsivecell membraneoncolytic virusvacciniaerythrocyte
spellingShingle Kaelan T. Samoranos
Alexandra L. Krisiewicz
Bianca C. Karpinecz
Philip A. Glover
Trevor V. Gale
Carla Chehadeh
Sheikh Ashshan
Richard Koya
Eddie Y. Chung
Han L. Lim
pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus
cancer
pH responsive
cell membrane
oncolytic virus
vaccinia
erythrocyte
title pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus
title_full pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus
title_fullStr pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus
title_full_unstemmed pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus
title_short pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus
title_sort ph sensitive erythrocyte derived membrane for acute systemic retention and increased infectivity of coated oncolytic vaccinia virus
topic cancer
pH responsive
cell membrane
oncolytic virus
vaccinia
erythrocyte
url https://www.mdpi.com/1999-4923/14/9/1810
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