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Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines

Oncolytic viruses (OVs) are a form of immunotherapy that release tumor antigens in the context of highly immunogenic viral signals following tumor-targeted infection and destruction. Emerging preclinical and clinical evidence suggests that this in situ vaccine effect is critical for successful viro-...

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Autores principales: Niavarani, Seyedeh Raheleh, Lawson, Christine, Tai, Lee-Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563237/
https://www.ncbi.nlm.nih.gov/pubmed/31083491
http://dx.doi.org/10.3390/v11050434
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author Niavarani, Seyedeh Raheleh
Lawson, Christine
Tai, Lee-Hwa
author_facet Niavarani, Seyedeh Raheleh
Lawson, Christine
Tai, Lee-Hwa
author_sort Niavarani, Seyedeh Raheleh
collection PubMed
description Oncolytic viruses (OVs) are a form of immunotherapy that release tumor antigens in the context of highly immunogenic viral signals following tumor-targeted infection and destruction. Emerging preclinical and clinical evidence suggests that this in situ vaccine effect is critical for successful viro-immunotherapy. In this review, we discuss the application of OV as an infected cell vaccine (ICV) as one method of enhancing the potency and breadth of anti-tumoral immunity. We focus on understanding and manipulating the critical role of natural killer (NK) cells and their interactions with other immune cells to promote a clinical outcome. With a synergistic tumor killing and immune activating mechanism, ICVs represent a valuable new addition to the cancer fighting toolbox with the potential to treat malignant disease.
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spelling pubmed-65632372019-06-17 Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines Niavarani, Seyedeh Raheleh Lawson, Christine Tai, Lee-Hwa Viruses Review Oncolytic viruses (OVs) are a form of immunotherapy that release tumor antigens in the context of highly immunogenic viral signals following tumor-targeted infection and destruction. Emerging preclinical and clinical evidence suggests that this in situ vaccine effect is critical for successful viro-immunotherapy. In this review, we discuss the application of OV as an infected cell vaccine (ICV) as one method of enhancing the potency and breadth of anti-tumoral immunity. We focus on understanding and manipulating the critical role of natural killer (NK) cells and their interactions with other immune cells to promote a clinical outcome. With a synergistic tumor killing and immune activating mechanism, ICVs represent a valuable new addition to the cancer fighting toolbox with the potential to treat malignant disease. MDPI 2019-05-11 /pmc/articles/PMC6563237/ /pubmed/31083491 http://dx.doi.org/10.3390/v11050434 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Niavarani, Seyedeh Raheleh
Lawson, Christine
Tai, Lee-Hwa
Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines
title Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines
title_full Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines
title_fullStr Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines
title_full_unstemmed Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines
title_short Treatment of Metastatic Disease through Natural Killer Cell Modulation by Infected Cell Vaccines
title_sort treatment of metastatic disease through natural killer cell modulation by infected cell vaccines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563237/
https://www.ncbi.nlm.nih.gov/pubmed/31083491
http://dx.doi.org/10.3390/v11050434
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