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Antigenic Essence: Upgrade of Cellular Cancer Vaccines

SIMPLE SUMMARY: Early cancer vaccines include whole-cell formulations, which operate on the principle that you should vaccinate with what you want to develop protection against. Such vaccines have been widely tested in various cancers and their advantages described but have not yet managed to pass c...

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Autores principales: Lokhov, Petr G., Balashova, Elena E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917603/
https://www.ncbi.nlm.nih.gov/pubmed/33673325
http://dx.doi.org/10.3390/cancers13040774
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author Lokhov, Petr G.
Balashova, Elena E.
author_facet Lokhov, Petr G.
Balashova, Elena E.
author_sort Lokhov, Petr G.
collection PubMed
description SIMPLE SUMMARY: Early cancer vaccines include whole-cell formulations, which operate on the principle that you should vaccinate with what you want to develop protection against. Such vaccines have been widely tested in various cancers and their advantages described but have not yet managed to pass clinical trials. Antigenic essence technology offers the possibility to revitalize the field of whole-cell-based vaccination, as the essence comprises the entire diversity of native cellular antigens. At the same time, the technology allows for precise control and purposeful change of essence composition as well as purification of essence from ballast cellular substances and also addresses issues of major histocompatibility complex restriction. Antigenic essence technology makes it possible to update many cellular vaccines that have already been developed, as well as to develop new ones, therefore introducing a new direction for anticancer vaccination research. ABSTRACT: The development of anticancer immunotherapy is characterized by several approaches, the most recognized of which include cellular vaccines, tumor-associated antigens (TAAs), neoantigens, and chimeric antigen receptor T cells (CAR-T). This paper presents antigenic essence technology as an effective means for the production of new antigen compositions for anticancer vaccination. This technology is developed via proteomics, cell culture technology, and immunological assays. In terms of vaccine development, it does not fit into any of the above-noted approaches and can be considered a new direction. Here we review the development of this technology, its main characteristics, comparison with existing approaches, and the features that distinguish it as a novel approach to anticancer vaccination. This review will also highlight the benefits of this technology over other approaches, such as the ability to control composition, optimize immunogenicity and similarity to target cells, and evade major histocompatibility complex restriction. The first antigenic essence products, presented under the SANTAVAC brand, are also described.
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spelling pubmed-79176032021-03-02 Antigenic Essence: Upgrade of Cellular Cancer Vaccines Lokhov, Petr G. Balashova, Elena E. Cancers (Basel) Review SIMPLE SUMMARY: Early cancer vaccines include whole-cell formulations, which operate on the principle that you should vaccinate with what you want to develop protection against. Such vaccines have been widely tested in various cancers and their advantages described but have not yet managed to pass clinical trials. Antigenic essence technology offers the possibility to revitalize the field of whole-cell-based vaccination, as the essence comprises the entire diversity of native cellular antigens. At the same time, the technology allows for precise control and purposeful change of essence composition as well as purification of essence from ballast cellular substances and also addresses issues of major histocompatibility complex restriction. Antigenic essence technology makes it possible to update many cellular vaccines that have already been developed, as well as to develop new ones, therefore introducing a new direction for anticancer vaccination research. ABSTRACT: The development of anticancer immunotherapy is characterized by several approaches, the most recognized of which include cellular vaccines, tumor-associated antigens (TAAs), neoantigens, and chimeric antigen receptor T cells (CAR-T). This paper presents antigenic essence technology as an effective means for the production of new antigen compositions for anticancer vaccination. This technology is developed via proteomics, cell culture technology, and immunological assays. In terms of vaccine development, it does not fit into any of the above-noted approaches and can be considered a new direction. Here we review the development of this technology, its main characteristics, comparison with existing approaches, and the features that distinguish it as a novel approach to anticancer vaccination. This review will also highlight the benefits of this technology over other approaches, such as the ability to control composition, optimize immunogenicity and similarity to target cells, and evade major histocompatibility complex restriction. The first antigenic essence products, presented under the SANTAVAC brand, are also described. MDPI 2021-02-12 /pmc/articles/PMC7917603/ /pubmed/33673325 http://dx.doi.org/10.3390/cancers13040774 Text en © 2021 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
Lokhov, Petr G.
Balashova, Elena E.
Antigenic Essence: Upgrade of Cellular Cancer Vaccines
title Antigenic Essence: Upgrade of Cellular Cancer Vaccines
title_full Antigenic Essence: Upgrade of Cellular Cancer Vaccines
title_fullStr Antigenic Essence: Upgrade of Cellular Cancer Vaccines
title_full_unstemmed Antigenic Essence: Upgrade of Cellular Cancer Vaccines
title_short Antigenic Essence: Upgrade of Cellular Cancer Vaccines
title_sort antigenic essence: upgrade of cellular cancer vaccines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917603/
https://www.ncbi.nlm.nih.gov/pubmed/33673325
http://dx.doi.org/10.3390/cancers13040774
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