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Translational nanoparticle engineering for cancer vaccines
Conventional cancer treatments remain insufficient to treat many therapy-resistant tumors.(1) Cancer vaccines attempt to overcome this resistance by activating the patient's immune system to eliminate tumor cells without the toxicity of systemic chemotherapy and radiation. Nanoparticles (NPs) a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665077/ https://www.ncbi.nlm.nih.gov/pubmed/29123947 http://dx.doi.org/10.1080/2162402X.2017.1290036 |
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author | Grippin, Adam J. Sayour, Elias J. Mitchell, Duane A. |
author_facet | Grippin, Adam J. Sayour, Elias J. Mitchell, Duane A. |
author_sort | Grippin, Adam J. |
collection | PubMed |
description | Conventional cancer treatments remain insufficient to treat many therapy-resistant tumors.(1) Cancer vaccines attempt to overcome this resistance by activating the patient's immune system to eliminate tumor cells without the toxicity of systemic chemotherapy and radiation. Nanoparticles (NPs) are promising as customizable, immunostimulatory carriers to protect and deliver antigen. Although many NP vaccines have been investigated in preclinical settings, a few have advanced into clinical application, and still fewer have demonstrated clinical benefit. This review incorporates observations from NP vaccines that have been evaluated in early phase clinical trials to make recommendations for the next generation of NP-based cancer vaccines. |
format | Online Article Text |
id | pubmed-5665077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-56650772017-11-09 Translational nanoparticle engineering for cancer vaccines Grippin, Adam J. Sayour, Elias J. Mitchell, Duane A. Oncoimmunology Review Conventional cancer treatments remain insufficient to treat many therapy-resistant tumors.(1) Cancer vaccines attempt to overcome this resistance by activating the patient's immune system to eliminate tumor cells without the toxicity of systemic chemotherapy and radiation. Nanoparticles (NPs) are promising as customizable, immunostimulatory carriers to protect and deliver antigen. Although many NP vaccines have been investigated in preclinical settings, a few have advanced into clinical application, and still fewer have demonstrated clinical benefit. This review incorporates observations from NP vaccines that have been evaluated in early phase clinical trials to make recommendations for the next generation of NP-based cancer vaccines. Taylor & Francis 2017-02-22 /pmc/articles/PMC5665077/ /pubmed/29123947 http://dx.doi.org/10.1080/2162402X.2017.1290036 Text en © 2017 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Review Grippin, Adam J. Sayour, Elias J. Mitchell, Duane A. Translational nanoparticle engineering for cancer vaccines |
title | Translational nanoparticle engineering for cancer vaccines |
title_full | Translational nanoparticle engineering for cancer vaccines |
title_fullStr | Translational nanoparticle engineering for cancer vaccines |
title_full_unstemmed | Translational nanoparticle engineering for cancer vaccines |
title_short | Translational nanoparticle engineering for cancer vaccines |
title_sort | translational nanoparticle engineering for cancer vaccines |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665077/ https://www.ncbi.nlm.nih.gov/pubmed/29123947 http://dx.doi.org/10.1080/2162402X.2017.1290036 |
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