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Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens
Therapeutic options for the treatment of colorectal cancer (CRC) are diverse but still not always satisfying. Recent success of immune checkpoint inhibition treatment for the subgroup of CRC patients suffering from hyper-mutated tumors suggests a permanent role of immune therapy in the clinical mana...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319136/ https://www.ncbi.nlm.nih.gov/pubmed/30622371 http://dx.doi.org/10.3748/wjg.v24.i48.5418 |
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author | Wagner, Sandra Mullins, Christina S Linnebacher, Michael |
author_facet | Wagner, Sandra Mullins, Christina S Linnebacher, Michael |
author_sort | Wagner, Sandra |
collection | PubMed |
description | Therapeutic options for the treatment of colorectal cancer (CRC) are diverse but still not always satisfying. Recent success of immune checkpoint inhibition treatment for the subgroup of CRC patients suffering from hyper-mutated tumors suggests a permanent role of immune therapy in the clinical management of CRC. Substantial improvement in treatment outcome could be achieved by development of efficient patient-individual CRC vaccination strategies. This mini-review summarizes the current knowledge on the two general classes of targets: tumor-associated antigens (TAAs) and tumor-specific antigens. TAAs like carcinoembryonic antigen and melanoma associated antigen are present in and shared by a subgroup of patients and a variety of clinical studies examined the efficacy of different TAA-derived peptide vaccines. Combinations of several TAAs as the next step and the development of personalized TAA-based peptide vaccines are discussed. Improvements of peptide-based vaccines achievable by adjuvants and immune-stimulatory chemotherapeutics are highlighted. Finally, we sum up clinical studies using tumor-specific antigens - in CRC almost exclusively neoantigens - which revealed promising results; particularly no severe adverse events were reported so far. Critical progress for clinical outcomes can be expected by individualizing neoantigen-based peptide vaccines and combining them with immune-stimulatory chemotherapeutics and immune checkpoint inhibitors. In light of these data and latest developments, truly personalized neoantigen-based peptide vaccines can be expected to fulfill modern precision medicine’s requirements and will manifest as treatment pillar for routine clinical management of CRC. |
format | Online Article Text |
id | pubmed-6319136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-63191362019-01-08 Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens Wagner, Sandra Mullins, Christina S Linnebacher, Michael World J Gastroenterol Review Therapeutic options for the treatment of colorectal cancer (CRC) are diverse but still not always satisfying. Recent success of immune checkpoint inhibition treatment for the subgroup of CRC patients suffering from hyper-mutated tumors suggests a permanent role of immune therapy in the clinical management of CRC. Substantial improvement in treatment outcome could be achieved by development of efficient patient-individual CRC vaccination strategies. This mini-review summarizes the current knowledge on the two general classes of targets: tumor-associated antigens (TAAs) and tumor-specific antigens. TAAs like carcinoembryonic antigen and melanoma associated antigen are present in and shared by a subgroup of patients and a variety of clinical studies examined the efficacy of different TAA-derived peptide vaccines. Combinations of several TAAs as the next step and the development of personalized TAA-based peptide vaccines are discussed. Improvements of peptide-based vaccines achievable by adjuvants and immune-stimulatory chemotherapeutics are highlighted. Finally, we sum up clinical studies using tumor-specific antigens - in CRC almost exclusively neoantigens - which revealed promising results; particularly no severe adverse events were reported so far. Critical progress for clinical outcomes can be expected by individualizing neoantigen-based peptide vaccines and combining them with immune-stimulatory chemotherapeutics and immune checkpoint inhibitors. In light of these data and latest developments, truly personalized neoantigen-based peptide vaccines can be expected to fulfill modern precision medicine’s requirements and will manifest as treatment pillar for routine clinical management of CRC. Baishideng Publishing Group Inc 2018-12-28 2018-12-28 /pmc/articles/PMC6319136/ /pubmed/30622371 http://dx.doi.org/10.3748/wjg.v24.i48.5418 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Review Wagner, Sandra Mullins, Christina S Linnebacher, Michael Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens |
title | Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens |
title_full | Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens |
title_fullStr | Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens |
title_full_unstemmed | Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens |
title_short | Colorectal cancer vaccines: Tumor-associated antigens vs neoantigens |
title_sort | colorectal cancer vaccines: tumor-associated antigens vs neoantigens |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319136/ https://www.ncbi.nlm.nih.gov/pubmed/30622371 http://dx.doi.org/10.3748/wjg.v24.i48.5418 |
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