Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines

Virus-like particles (VLP) spontaneously assemble from viral structural proteins. They are naturally biocompatible and non-infectious. VLP can serve as a platform for many potential vaccine epitopes, display them in a dense repeating array, and elicit antibodies against non-immunogenic substances, i...

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Hlavní autoři: Jerri C. Caldeira, Michael Perrine, Federica Pericle, Federica Cavallo
Médium: Článek
Jazyk:English
Vydáno: MDPI AG 2020-04-01
Edice:Viruses
Témata:
On-line přístup:https://www.mdpi.com/1999-4915/12/5/488
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author Jerri C. Caldeira
Michael Perrine
Federica Pericle
Federica Cavallo
author_facet Jerri C. Caldeira
Michael Perrine
Federica Pericle
Federica Cavallo
author_sort Jerri C. Caldeira
collection DOAJ
description Virus-like particles (VLP) spontaneously assemble from viral structural proteins. They are naturally biocompatible and non-infectious. VLP can serve as a platform for many potential vaccine epitopes, display them in a dense repeating array, and elicit antibodies against non-immunogenic substances, including tumor-associated self-antigens. Genetic or chemical conjugation facilitates the multivalent display of a homologous or heterologous epitope. Most VLP range in diameter from 25 to 100 nm and, in most cases, drain freely into the lymphatic vessels and induce antibodies with high titers and affinity without the need for additional adjuvants. VLP administration can be performed using different strategies, regimens, and doses to improve the immunogenicity of the antigen they expose on their surface. This article summarizes the features of VLP and presents them as a relevant platform technology to address not only infectious diseases but also chronic diseases and cancer.
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spelling doaj.art-3948abfc6bdb4a20b51bad939e6f9f9d2023-11-19T22:48:36ZengMDPI AGViruses1999-49152020-04-0112548810.3390/v12050488Virus-Like Particles as an Immunogenic Platform for Cancer VaccinesJerri C. Caldeira0Michael Perrine1Federica Pericle2Federica Cavallo3AgilVax, Inc., Albuquerque, NM 87110, USAAgilVax, Inc., Albuquerque, NM 87110, USABorder Biomedical Research Center, University of Texas at El Paso, El Paso, TX 79968, USADepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, 10124 Torino, ItalyVirus-like particles (VLP) spontaneously assemble from viral structural proteins. They are naturally biocompatible and non-infectious. VLP can serve as a platform for many potential vaccine epitopes, display them in a dense repeating array, and elicit antibodies against non-immunogenic substances, including tumor-associated self-antigens. Genetic or chemical conjugation facilitates the multivalent display of a homologous or heterologous epitope. Most VLP range in diameter from 25 to 100 nm and, in most cases, drain freely into the lymphatic vessels and induce antibodies with high titers and affinity without the need for additional adjuvants. VLP administration can be performed using different strategies, regimens, and doses to improve the immunogenicity of the antigen they expose on their surface. This article summarizes the features of VLP and presents them as a relevant platform technology to address not only infectious diseases but also chronic diseases and cancer.https://www.mdpi.com/1999-4915/12/5/488virus-like particlesvaccinecancerimmunotherapy
spellingShingle Jerri C. Caldeira
Michael Perrine
Federica Pericle
Federica Cavallo
Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines
Viruses
virus-like particles
vaccine
cancer
immunotherapy
title Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines
title_full Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines
title_fullStr Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines
title_full_unstemmed Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines
title_short Virus-Like Particles as an Immunogenic Platform for Cancer Vaccines
title_sort virus like particles as an immunogenic platform for cancer vaccines
topic virus-like particles
vaccine
cancer
immunotherapy
url https://www.mdpi.com/1999-4915/12/5/488
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