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Oncolytic virotherapy in hematopoietic stem cell transplantation.

Authors :
Kazemi MH
Kuhestani Dehaghi B
Roshandel E
Parkhideh S
Mehdizadeh M
Salimi M
Hajifathali A
Hamidpour M
Source :
Human immunology [Hum Immunol] 2021 Sep; Vol. 82 (9), pp. 640-648. Date of Electronic Publication: 2021 Jun 09.
Publication Year :
2021

Abstract

Hematopoietic stem cell transplantation (HSCT) is a curative option for various hematologic malignancies. However, fatal complications, such as relapse and graft-versus-host disease (GVHD) hampered favorable HSCT outcomes. Cancer cells remained in the body following the conditioning regimen, or those contaminating the autologous graft can cause relapse. Although the relapse is much lesser in allogeneic HSCT, GVHD is still a life-threatening complication in this type of HSCT. Researchers are seeking various strategies to reduce relapse and GVHD in HSCT with minimum effects on the engraftment and immune-reconstitution. Oncolytic viruses (OVs) are emerging anti-cancer agents with promising results in battling solid tumors. OVs can selectively replicate in the malignant cells in which the antiviral immune responses have defected. Hence, they could be used as a purging agent to eradicate the tumoral contamination of autologous grafts with no damages to hematopoietic stem cells. Moreover, they have been shown to alleviate GVHD complications through modulating alloreactive T cell responses. Primary results promise using OVs as a strategy to reduce both relapse and GVHD in the HSCT without affecting hematologic and immunologic engraftment. Herein, we provide the latest findings in the field of OV therapy in HSCT and discuss their pros and cons.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2021 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1879-1166
Volume :
82
Issue :
9
Database :
MEDLINE
Journal :
Human immunology
Publication Type :
Academic Journal
Accession number :
34119352
Full Text :
https://doi.org/10.1016/j.humimm.2021.05.007