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Oncolytic Immunotherapy: Where Are We Clinically?

Following a century of preclinical and clinical work, oncolytic viruses are now proving themselves in randomized phase 3 trials. Interestingly, human data indicates that these agents have potent immunostimulatory activity, raising the possibility that the key consequence of oncolysis might be induct...

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Detalles Bibliográficos
Autor principal: Hemminki, Akseli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914551/
https://www.ncbi.nlm.nih.gov/pubmed/24551478
http://dx.doi.org/10.1155/2014/862925
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author Hemminki, Akseli
author_facet Hemminki, Akseli
author_sort Hemminki, Akseli
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description Following a century of preclinical and clinical work, oncolytic viruses are now proving themselves in randomized phase 3 trials. Interestingly, human data indicates that these agents have potent immunostimulatory activity, raising the possibility that the key consequence of oncolysis might be induction of antitumor immunity, especially in the context of viruses harboring immunostimulatory transgenes. While safety and efficacy of many types of oncolytic viruses, including adenovirus, herpes, reo, and vaccinia seem promising, few mechanisms of action studies have been performed with human substrates. Thus, the relative contribution of “pure” oncolysis, the immune response resulting from oncolysis, and the added benefit of adding a transgene remain poorly understood. Here, the available clinical data on oncolytic viruses is reviewed, with emphasis on immunological aspects.
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spelling pubmed-39145512014-02-18 Oncolytic Immunotherapy: Where Are We Clinically? Hemminki, Akseli Scientifica (Cairo) Review Article Following a century of preclinical and clinical work, oncolytic viruses are now proving themselves in randomized phase 3 trials. Interestingly, human data indicates that these agents have potent immunostimulatory activity, raising the possibility that the key consequence of oncolysis might be induction of antitumor immunity, especially in the context of viruses harboring immunostimulatory transgenes. While safety and efficacy of many types of oncolytic viruses, including adenovirus, herpes, reo, and vaccinia seem promising, few mechanisms of action studies have been performed with human substrates. Thus, the relative contribution of “pure” oncolysis, the immune response resulting from oncolysis, and the added benefit of adding a transgene remain poorly understood. Here, the available clinical data on oncolytic viruses is reviewed, with emphasis on immunological aspects. Hindawi Publishing Corporation 2014 2014-01-16 /pmc/articles/PMC3914551/ /pubmed/24551478 http://dx.doi.org/10.1155/2014/862925 Text en Copyright © 2014 Akseli Hemminki. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hemminki, Akseli
Oncolytic Immunotherapy: Where Are We Clinically?
title Oncolytic Immunotherapy: Where Are We Clinically?
title_full Oncolytic Immunotherapy: Where Are We Clinically?
title_fullStr Oncolytic Immunotherapy: Where Are We Clinically?
title_full_unstemmed Oncolytic Immunotherapy: Where Are We Clinically?
title_short Oncolytic Immunotherapy: Where Are We Clinically?
title_sort oncolytic immunotherapy: where are we clinically?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914551/
https://www.ncbi.nlm.nih.gov/pubmed/24551478
http://dx.doi.org/10.1155/2014/862925
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