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Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors
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 strom...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989711/ https://www.ncbi.nlm.nih.gov/pubmed/35434272 http://dx.doi.org/10.1016/j.omto.2022.03.008 |
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author | Yoon, A-Rum Rivera-Cruz, Cosette Gimble, Jeffrey M. Yun, Chae-Ok Figueiredo, Marxa L. |
author_facet | Yoon, A-Rum Rivera-Cruz, Cosette Gimble, Jeffrey M. Yun, Chae-Ok Figueiredo, Marxa L. |
author_sort | Yoon, A-Rum |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8989711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-89897112022-04-15 Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors Yoon, A-Rum Rivera-Cruz, Cosette Gimble, Jeffrey M. Yun, Chae-Ok Figueiredo, Marxa L. Mol Ther Oncolytics Review 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. American Society of Gene & Cell Therapy 2022-03-19 /pmc/articles/PMC8989711/ /pubmed/35434272 http://dx.doi.org/10.1016/j.omto.2022.03.008 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Yoon, A-Rum Rivera-Cruz, Cosette Gimble, Jeffrey M. Yun, Chae-Ok Figueiredo, Marxa L. Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
title | Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
title_full | Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
title_fullStr | Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
title_full_unstemmed | Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
title_short | Immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
title_sort | immunotherapy by mesenchymal stromal cell delivery of oncolytic viruses for treating metastatic tumors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989711/ https://www.ncbi.nlm.nih.gov/pubmed/35434272 http://dx.doi.org/10.1016/j.omto.2022.03.008 |
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