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Potential association factors for developing effective peptide-based cancer vaccines

Peptide-based cancer vaccines have been shown to boost immune systems to kill tumor cells in cancer patients. However, designing an effective T cell epitope peptide-based cancer vaccine still remains a challenge and is a major hurdle for the application of cancer vaccines. In this study, we construc...

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Autores principales: Jiang, Chongming, Li, Jianrong, Zhang, Wei, Zhuang, Zhenkun, Liu, Geng, Hong, Wei, Li, Bo, Zhang, Xiuqing, Chao, Cheng-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364268/
https://www.ncbi.nlm.nih.gov/pubmed/35967400
http://dx.doi.org/10.3389/fimmu.2022.931612
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author Jiang, Chongming
Li, Jianrong
Zhang, Wei
Zhuang, Zhenkun
Liu, Geng
Hong, Wei
Li, Bo
Zhang, Xiuqing
Chao, Cheng-Chi
author_facet Jiang, Chongming
Li, Jianrong
Zhang, Wei
Zhuang, Zhenkun
Liu, Geng
Hong, Wei
Li, Bo
Zhang, Xiuqing
Chao, Cheng-Chi
author_sort Jiang, Chongming
collection PubMed
description Peptide-based cancer vaccines have been shown to boost immune systems to kill tumor cells in cancer patients. However, designing an effective T cell epitope peptide-based cancer vaccine still remains a challenge and is a major hurdle for the application of cancer vaccines. In this study, we constructed for the first time a library of peptide-based cancer vaccines and their clinical attributes, named CancerVaccine (https://peptidecancervaccine.weebly.com/). To investigate the association factors that influence the effectiveness of cancer vaccines, these peptide-based cancer vaccines were classified into high (HCR) and low (LCR) clinical responses based on their clinical efficacy. Our study highlights that modified peptides derived from artificially modified proteins are suitable as cancer vaccines, especially for melanoma. It may be possible to advance cancer vaccines by screening for HLA class II affinity peptides may be an effective therapeutic strategy. In addition, the treatment regimen has the potential to influence the clinical response of a cancer vaccine, and Montanide ISA-51 might be an effective adjuvant. Finally, we constructed a high sensitivity and specificity machine learning model to assist in designing peptide-based cancer vaccines capable of providing high clinical responses. Together, our findings illustrate that a high clinical response following peptide-based cancer vaccination is correlated with the right type of peptide, the appropriate adjuvant, and a matched HLA allele, as well as an appropriate treatment regimen. This study would allow for enhanced development of cancer vaccines.
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spelling pubmed-93642682022-08-11 Potential association factors for developing effective peptide-based cancer vaccines Jiang, Chongming Li, Jianrong Zhang, Wei Zhuang, Zhenkun Liu, Geng Hong, Wei Li, Bo Zhang, Xiuqing Chao, Cheng-Chi Front Immunol Immunology Peptide-based cancer vaccines have been shown to boost immune systems to kill tumor cells in cancer patients. However, designing an effective T cell epitope peptide-based cancer vaccine still remains a challenge and is a major hurdle for the application of cancer vaccines. In this study, we constructed for the first time a library of peptide-based cancer vaccines and their clinical attributes, named CancerVaccine (https://peptidecancervaccine.weebly.com/). To investigate the association factors that influence the effectiveness of cancer vaccines, these peptide-based cancer vaccines were classified into high (HCR) and low (LCR) clinical responses based on their clinical efficacy. Our study highlights that modified peptides derived from artificially modified proteins are suitable as cancer vaccines, especially for melanoma. It may be possible to advance cancer vaccines by screening for HLA class II affinity peptides may be an effective therapeutic strategy. In addition, the treatment regimen has the potential to influence the clinical response of a cancer vaccine, and Montanide ISA-51 might be an effective adjuvant. Finally, we constructed a high sensitivity and specificity machine learning model to assist in designing peptide-based cancer vaccines capable of providing high clinical responses. Together, our findings illustrate that a high clinical response following peptide-based cancer vaccination is correlated with the right type of peptide, the appropriate adjuvant, and a matched HLA allele, as well as an appropriate treatment regimen. This study would allow for enhanced development of cancer vaccines. Frontiers Media S.A. 2022-07-27 /pmc/articles/PMC9364268/ /pubmed/35967400 http://dx.doi.org/10.3389/fimmu.2022.931612 Text en Copyright © 2022 Jiang, Li, Zhang, Zhuang, Liu, Hong, Li, Zhang and Chao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Jiang, Chongming
Li, Jianrong
Zhang, Wei
Zhuang, Zhenkun
Liu, Geng
Hong, Wei
Li, Bo
Zhang, Xiuqing
Chao, Cheng-Chi
Potential association factors for developing effective peptide-based cancer vaccines
title Potential association factors for developing effective peptide-based cancer vaccines
title_full Potential association factors for developing effective peptide-based cancer vaccines
title_fullStr Potential association factors for developing effective peptide-based cancer vaccines
title_full_unstemmed Potential association factors for developing effective peptide-based cancer vaccines
title_short Potential association factors for developing effective peptide-based cancer vaccines
title_sort potential association factors for developing effective peptide-based cancer vaccines
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364268/
https://www.ncbi.nlm.nih.gov/pubmed/35967400
http://dx.doi.org/10.3389/fimmu.2022.931612
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