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

被引:12
|
作者
Yoon, A-Rum [2 ,4 ]
Rivera-Cruz, Cosette [1 ]
Gimble, Jeffrey M. [1 ,3 ]
Yun, Chae-Ok [2 ,4 ,5 ]
Figueiredo, Marxa L. [1 ]
机构
[1] Purdue Univ, Dept Basic Med Sci, Coll Vet Med, 625 Harrison St, W Lafayette, IN 47907 USA
[2] Hanyang Univ, Coll Engn, Dept Bioengn, 222 Wangsimni Ro, Seoul 04763, South Korea
[3] Obatala Sci Inc, New Orleans, LA 70148 USA
[4] Hanyang Univ, Inst Nano Sci & Technol INST, 222 Wangsimni Ro, Seoul 04763, South Korea
[5] GeneMedicine Co Ltd, Seoul 04763, South Korea
来源
基金
新加坡国家研究基金会;
关键词
ENDOTHELIAL GROWTH-FACTOR; STEM-CELLS; BONE-MARROW; INTERNATIONAL-SOCIETY; GENE DELIVERY; PHASE-I; THERAPEUTIC-EFFICACY; CONDITIONED MEDIUM; EXPRESSING IL-12; CANCER CELLS;
D O I
10.1016/j.omto.2022.03.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 antitumor 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.
引用
收藏
页码:78 / 97
页数:20
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