TY - JOUR
T1 - Locked and loaded
T2 - engineering and arming oncolytic adenoviruses to enhance anti-tumor immune responses
AU - Lu, Shao Chia
AU - Barry, Michael A.
N1 - Funding Information:
This project was supported by the Congressionally Directed Medical Research Program (W81XWH-19-1-0756), the Mayo Graduate School of Biomedical Sciences, and the Walter & Lucille Rubin Fund in Infectious Diseases Honoring Michael Camilleri, M.D. at Mayo Clinic.
Publisher Copyright:
© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Introduction: Oncolytic adenoviruses (Ads) are promising therapeutics to enhance anti-tumor immune responses and modulate the immune-suppressive tumor microenvironment (TME). Due to their potent ability to deliver genes in vivo, oncolytic Ads have been armed with a variety of immune stimulatory payloads to boost tumor immunotherapy. Areas covered: We describe current knowledge about engineering oncolytic Ads to insert transgene payloads, including methods to increase its genome capacity for transgene insertion. We also review several categories of immune stimulatory payloads that have been used in oncolytic Ads to combat different barriers to effective immunotherapy. Expert opinion: We anticipate that multi-armed oncolytic Ads alone or in combination with other types of immunotherapies will greatly improve the efficacy of oncolytic virotherapy in the future by targeting several immune barriers. However, the production and testing of multiple payload-armed Ads can be complex and time-consuming due to the limitations of current tools. Given this, we should develop new tools for rapid construction of armed Ads, improve animal models or new systems to compare the efficacy of multiple payloads, and carefully monitor the immunological toxicity induced by payloads or by systemic delivery. Most importantly, we should pursue payload-arming approaches with great care to ensure safety.
AB - Introduction: Oncolytic adenoviruses (Ads) are promising therapeutics to enhance anti-tumor immune responses and modulate the immune-suppressive tumor microenvironment (TME). Due to their potent ability to deliver genes in vivo, oncolytic Ads have been armed with a variety of immune stimulatory payloads to boost tumor immunotherapy. Areas covered: We describe current knowledge about engineering oncolytic Ads to insert transgene payloads, including methods to increase its genome capacity for transgene insertion. We also review several categories of immune stimulatory payloads that have been used in oncolytic Ads to combat different barriers to effective immunotherapy. Expert opinion: We anticipate that multi-armed oncolytic Ads alone or in combination with other types of immunotherapies will greatly improve the efficacy of oncolytic virotherapy in the future by targeting several immune barriers. However, the production and testing of multiple payload-armed Ads can be complex and time-consuming due to the limitations of current tools. Given this, we should develop new tools for rapid construction of armed Ads, improve animal models or new systems to compare the efficacy of multiple payloads, and carefully monitor the immunological toxicity induced by payloads or by systemic delivery. Most importantly, we should pursue payload-arming approaches with great care to ensure safety.
KW - barriers to cancer immunotherapy
KW - combination cancer immunotherapy
KW - immune checkpoints
KW - immune payloads
KW - Oncolytic adenoviruses
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U2 - 10.1080/14712598.2022.2139601
DO - 10.1080/14712598.2022.2139601
M3 - Review article
C2 - 36300528
AN - SCOPUS:85141853107
SN - 1471-2598
VL - 22
SP - 1359
EP - 1378
JO - Expert Opinion on Biological Therapy
JF - Expert Opinion on Biological Therapy
IS - 11
ER -