TY - JOUR
T1 - Immunovirotherapy Based on Recombinant Vesicular Stomatitis Virus
T2 - Where Are We?
AU - Zhang, Yuguo
AU - Nagalo, Bolni Marius
N1 - Funding Information:
This work was supported by the National Institutes of Health (NIH) through a National Cancer Institute (NCI) grant (CA234324 to BN) and start-up funds from the Winthrop P. Rockefeller Cancer Institute at the University of Arkansas for Medical Sciences to BN. The article contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.
Publisher Copyright:
Copyright © 2022 Zhang and Nagalo.
PY - 2022/6/28
Y1 - 2022/6/28
N2 - Vesicular stomatitis virus (VSV), a negative-strand RNA virus of the Vesiculovirus genus, has demonstrated encouraging anti-neoplastic activity across multiple human cancer types. VSV is particularly attractive as an oncolytic agent because of its broad tropism, fast replication kinetics, and amenability to genetic manipulations. Furthermore, VSV-induced oncolysis can elicit a potent antitumor cytotoxic T-cell response to viral proteins and tumor-associated antigens, resulting in a long-lasting antitumor effect. Because of this multifaceted immunomodulatory property, VSV was investigated extensively as an immunovirotherapy alone or combined with other anticancer modalities, such as immune checkpoint blockade. Despite these recent opportunities to delineate synergistic and additive antitumor effects with existing anticancer therapies, FDA approval for the use of oncolytic VSV in humans has not yet been granted. This mini-review discusses factors that have prompted the use of VSV as an immunovirotherapy in human cancers and provides insights into future perspectives and research areas to improve VSV-based oncotherapy.
AB - Vesicular stomatitis virus (VSV), a negative-strand RNA virus of the Vesiculovirus genus, has demonstrated encouraging anti-neoplastic activity across multiple human cancer types. VSV is particularly attractive as an oncolytic agent because of its broad tropism, fast replication kinetics, and amenability to genetic manipulations. Furthermore, VSV-induced oncolysis can elicit a potent antitumor cytotoxic T-cell response to viral proteins and tumor-associated antigens, resulting in a long-lasting antitumor effect. Because of this multifaceted immunomodulatory property, VSV was investigated extensively as an immunovirotherapy alone or combined with other anticancer modalities, such as immune checkpoint blockade. Despite these recent opportunities to delineate synergistic and additive antitumor effects with existing anticancer therapies, FDA approval for the use of oncolytic VSV in humans has not yet been granted. This mini-review discusses factors that have prompted the use of VSV as an immunovirotherapy in human cancers and provides insights into future perspectives and research areas to improve VSV-based oncotherapy.
KW - cancer therapy
KW - genetically modified virus
KW - immunotherapy
KW - oncolytic virus
KW - vesicular stomatitis virus
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U2 - 10.3389/fimmu.2022.898631
DO - 10.3389/fimmu.2022.898631
M3 - Review article
C2 - 35837384
AN - SCOPUS:85133928190
SN - 1664-3224
VL - 13
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 898631
ER -