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Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumorsopen access

Authors
Yoon, A-RumRivera-Cruz, CosetteGimble, Jeffrey M.Yun, Chae-OkFigueiredo, Marxa L.
Issue Date
Jun-2022
Publisher
Cell Press
Keywords
enhanced delivery; immunotherapy; mesenchymal stromal cells; metastatic tumors; oncolytic viruses
Citation
Molecular Therapy - Oncolytics, v.25, pp.78 - 97
Indexed
SCIE
SCOPUS
Journal Title
Molecular Therapy - Oncolytics
Volume
25
Start Page
78
End Page
97
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/170134
DOI
10.1016/j.omto.2022.03.008
ISSN
2372-7705
Abstract
Oncolytic viruses (OVs) have emerged as a very promising anti-cancer therapeutic strategy in the past decades. However, despite their pre-clinical promise, many OV clinical evaluations for cancer therapy have highlighted the continued need for their improved delivery and targeting. Mesenchymal stromal cells (MSCs) have emerged as excellent candidate vehicles for the delivery of OVs due to their tumor-homing properties and low immunogenicity. MSCs can enhance OV delivery by protecting viruses from rapid clearance following administration and also by more efficiently targeting tumor sites, consequently augmenting the therapeutic potential of OVs. MSCs can function as “biological factories,” enabling OV amplification within these cells to promote tumor lysis following MSC-OV arrival at the tumor site. MSC-OVs can promote enhanced safety profiles and therapeutic effects relative to OVs alone. In this review we explore the general characteristics of MSCs as delivery tools for cancer therapeutic agents. Furthermore, we discuss the potential of OVs as immune therapeutics and highlight some of the promising applications stemming from combining MSCs to achieve enhanced delivery and anti-tumor effectiveness of OVs at different pre-clinical and clinical stages. We further provide potential pitfalls of the MSC-OV platform and the strategies under development for enhancing the efficacy of these emerging therapeutics.
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