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Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives

Therapeutic cancer vaccines are one of the most promising strategies of immunotherapy. Traditional vaccines consisting of tumor-associated antigens have met with limited success. Recently, neoantigens derived from nonsynonymous mutations in tumor cells have emerged as alternatives that can improve t...

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Detalles Bibliográficos
Autores principales: Chen, Xiaotong, Yang, Ju, Wang, Lifeng, Liu, Baorui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255011/
https://www.ncbi.nlm.nih.gov/pubmed/32483434
http://dx.doi.org/10.7150/thno.38742
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author Chen, Xiaotong
Yang, Ju
Wang, Lifeng
Liu, Baorui
author_facet Chen, Xiaotong
Yang, Ju
Wang, Lifeng
Liu, Baorui
author_sort Chen, Xiaotong
collection PubMed
description Therapeutic cancer vaccines are one of the most promising strategies of immunotherapy. Traditional vaccines consisting of tumor-associated antigens have met with limited success. Recently, neoantigens derived from nonsynonymous mutations in tumor cells have emerged as alternatives that can improve tumor-specificity and reduce on-target off-tumor toxicity. Synthetic peptides are a common platform for neoantigen vaccines. It has been suggested that extending short peptides into long peptides can overcome immune tolerance and induce both CD4(+) and CD8(+) T cell responses. This review will introduce the history of long peptide-based neoantigen vaccines, discuss their advantages, summarize current preclinical and clinical developments, and propose future perspectives.
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spelling pubmed-72550112020-05-31 Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives Chen, Xiaotong Yang, Ju Wang, Lifeng Liu, Baorui Theranostics Review Therapeutic cancer vaccines are one of the most promising strategies of immunotherapy. Traditional vaccines consisting of tumor-associated antigens have met with limited success. Recently, neoantigens derived from nonsynonymous mutations in tumor cells have emerged as alternatives that can improve tumor-specificity and reduce on-target off-tumor toxicity. Synthetic peptides are a common platform for neoantigen vaccines. It has been suggested that extending short peptides into long peptides can overcome immune tolerance and induce both CD4(+) and CD8(+) T cell responses. This review will introduce the history of long peptide-based neoantigen vaccines, discuss their advantages, summarize current preclinical and clinical developments, and propose future perspectives. Ivyspring International Publisher 2020-05-15 /pmc/articles/PMC7255011/ /pubmed/32483434 http://dx.doi.org/10.7150/thno.38742 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Chen, Xiaotong
Yang, Ju
Wang, Lifeng
Liu, Baorui
Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
title Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
title_full Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
title_fullStr Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
title_full_unstemmed Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
title_short Personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
title_sort personalized neoantigen vaccination with synthetic long peptides: recent advances and future perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255011/
https://www.ncbi.nlm.nih.gov/pubmed/32483434
http://dx.doi.org/10.7150/thno.38742
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