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Improved Safety of New MicroRNA-Regulated Oncolytic Coxsackievirus B3 Observed After Intravenous Administration in Colorectal-Tumor-Bearing Mice

Abstract:
Oncolytic coxsackievirus B3 (oCVB3) strain PD-H has shown potent oncolytic efficacy and a remarkable safety profile in the treatment of colorectal cancer in vivo after intratumoral (i.t.) injection. In this study, we investigated the safety and efficiency of PD-H following intravenous (i.v.) virus administration. When injected i.v. into Balb/C mice bearing subcutaneous Colon-26 tumors, PD-H led to slightly reduced tumor progression and a significant increase in animal survival, but it also caused multi-organ infection and tissue damage. To improve the safety profile of PD-H, we inserted microRNA target sites (miR-TS) of the heart-specific miR-1, pancreas-specific miR-375, liver-specific miR-122, and brain-specific miR-124 or the tumor-suppressor miR-145 into the genome of PD-H and generated the viruses PD-622TS and PD-145TS. Both viruses replicated similarly and induced cytotoxicity comparable to that of PD-H in the colorectal carcinoma cell lines Colon-26 and CT-26Luc. Their replication was inhibited in HEK293T cells transiently transfected with the cognate microRNAs. In vivo, i.v. administration of PD-145TS and PD-622TS to healthy Balb/C mouse resulted in significantly lower viral titers in the organs of mice and led to significantly less-intense pathological alterations compared to PD-H. PD-622TS injected i.v. into Balb/C mice with CT-26Luc-induced peritoneal carcinomatosis did not induce off-target alterations in normal organs, but it failed to induce a therapeutic effect. These data indicate that PD-H or microRNA-regulated PD derivatives exhibit only limited therapeutic efficacy following i.v. injection in colorectal tumor-bearing mice. However, the newly engineered microRNA-regulated PD-H variants demonstrate improved safety profiles.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3390/v18010143

Authors

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Role:
Author
ORCID:
0009-0008-7361-224X
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Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Sub department:
Oncology
Role:
Author
ORCID:
0000-0002-8552-2005
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Role:
Author
ORCID:
0009-0005-5089-8052


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Funder identifier:
https://ror.org/018mejw64
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Funder identifier:
https://ror.org/01wxdd722
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Funder identifier:
https://ror.org/02q83sc19


Publisher:
MDPI
Journal:
Viruses More from this journal
Volume:
18
Issue:
1
Pages:
143
Publication date:
2026-01-22
Acceptance date:
2026-01-20
DOI:
EISSN:
1999-4915
ISSN:
1999-4915
Pmid:
41600904


Language:
English
Keywords:
Pubs id:
2365797
UUID:
uuid_d6190ab4-6a51-4914-ba6c-87d78cd3c49d
Local pid:
pubs:2365797
Source identifiers:
3727802
Deposit date:
2026-02-05
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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