Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes

Cancer vaccines may be harnessed to incite immunity against poorly immunogenic tumors, however they have failed in therapeutic settings. Poor antigenicity coupled with systemic and intratumoral immune suppression have been significant drawbacks. RNA encoding for tumor associated or specific epitopes...

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Main Authors: Elias J. Sayour, Hector R. Mendez-Gomez, Duane A. Mitchell
Format: Article
Language:English
Published: MDPI AG 2018-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/19/10/2890
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author Elias J. Sayour
Hector R. Mendez-Gomez
Duane A. Mitchell
author_facet Elias J. Sayour
Hector R. Mendez-Gomez
Duane A. Mitchell
author_sort Elias J. Sayour
collection DOAJ
description Cancer vaccines may be harnessed to incite immunity against poorly immunogenic tumors, however they have failed in therapeutic settings. Poor antigenicity coupled with systemic and intratumoral immune suppression have been significant drawbacks. RNA encoding for tumor associated or specific epitopes can serve as a more immunogenic and expeditious trigger of anti-tumor immunity. RNA stimulates innate immunity through toll like receptor stimulation producing type I interferon, and it mediates potent adaptive responses. Since RNA is inherently unstable, delivery systems have been developed to protect and deliver it to intended targets in vivo. In this review, we discuss liposomes as RNA delivery vehicles and their role as cancer vaccines.
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spelling doaj.art-a2b4718f6d484e0981b80b665503cd232022-12-22T03:35:27ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-09-011910289010.3390/ijms19102890ijms19102890Cancer Vaccine Immunotherapy with RNA-Loaded LiposomesElias J. Sayour0Hector R. Mendez-Gomez1Duane A. Mitchell2Preston A. Wells, Jr. Center for Brain Tumor Therapy, University of Florida Brain Tumor Immunotherapy Program, Lilian S. Wells Department of Neurosurgery, 1149 South Newell Drive, McKnight Brain Institute, University of Florida, Gainesville, FL 32611, USAPreston A. Wells, Jr. Center for Brain Tumor Therapy, University of Florida Brain Tumor Immunotherapy Program, Lilian S. Wells Department of Neurosurgery, 1149 South Newell Drive, McKnight Brain Institute, University of Florida, Gainesville, FL 32611, USAPreston A. Wells, Jr. Center for Brain Tumor Therapy, University of Florida Brain Tumor Immunotherapy Program, Lilian S. Wells Department of Neurosurgery, 1149 South Newell Drive, McKnight Brain Institute, University of Florida, Gainesville, FL 32611, USACancer vaccines may be harnessed to incite immunity against poorly immunogenic tumors, however they have failed in therapeutic settings. Poor antigenicity coupled with systemic and intratumoral immune suppression have been significant drawbacks. RNA encoding for tumor associated or specific epitopes can serve as a more immunogenic and expeditious trigger of anti-tumor immunity. RNA stimulates innate immunity through toll like receptor stimulation producing type I interferon, and it mediates potent adaptive responses. Since RNA is inherently unstable, delivery systems have been developed to protect and deliver it to intended targets in vivo. In this review, we discuss liposomes as RNA delivery vehicles and their role as cancer vaccines.http://www.mdpi.com/1422-0067/19/10/2890immunotherapyliposomesRNAcancer vaccines
spellingShingle Elias J. Sayour
Hector R. Mendez-Gomez
Duane A. Mitchell
Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes
International Journal of Molecular Sciences
immunotherapy
liposomes
RNA
cancer vaccines
title Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes
title_full Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes
title_fullStr Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes
title_full_unstemmed Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes
title_short Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes
title_sort cancer vaccine immunotherapy with rna loaded liposomes
topic immunotherapy
liposomes
RNA
cancer vaccines
url http://www.mdpi.com/1422-0067/19/10/2890
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