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TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice
Cancer peptide vaccines are a promising cancer immunotherapy that can induce cancer-specific cytotoxic T lymphocytes (CTLs) in tumors. However, recent clinical trials of cancer vaccines have revealed that the efficacy of the vaccines is limited. Targeting single antigens and vaccination with short p...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560884/ https://www.ncbi.nlm.nih.gov/pubmed/33057061 http://dx.doi.org/10.1038/s41598-020-74187-6 |
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author | Tanaka, Yuki Wada, Hiroshi Goto, Risa Osada, Toshihiro Yamamura, Keisuke Fukaya, Satoshi Shimizu, Atsushi Okubo, Mitsuru Minamiguchi, Kazuhisa Ikizawa, Koichi Sasaki, Eiji Utsugi, Teruhiro |
author_facet | Tanaka, Yuki Wada, Hiroshi Goto, Risa Osada, Toshihiro Yamamura, Keisuke Fukaya, Satoshi Shimizu, Atsushi Okubo, Mitsuru Minamiguchi, Kazuhisa Ikizawa, Koichi Sasaki, Eiji Utsugi, Teruhiro |
author_sort | Tanaka, Yuki |
collection | PubMed |
description | Cancer peptide vaccines are a promising cancer immunotherapy that can induce cancer-specific cytotoxic T lymphocytes (CTLs) in tumors. However, recent clinical trials of cancer vaccines have revealed that the efficacy of the vaccines is limited. Targeting single antigens and vaccination with short peptides are partly the cause of the poor clinical outcomes. We synthesized a novel multi-epitope long peptide, TAS0314, which induced multiple epitope-specific CTLs in HLA knock-in mice. It also showed superior epitope-specific CTL induction and antitumor activity. We also established a combination treatment model of vaccination with PD-1/PD-L1 blockade in HLA-A*2402 knock-in mice, and it showed a synergistic antitumor effect with TAS0314. Thus, our data indicated that TAS0314 treatment, especially in combination with PD-1/PD-L1 blockade, is a promising therapeutic candidate for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-7560884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75608842020-10-19 TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice Tanaka, Yuki Wada, Hiroshi Goto, Risa Osada, Toshihiro Yamamura, Keisuke Fukaya, Satoshi Shimizu, Atsushi Okubo, Mitsuru Minamiguchi, Kazuhisa Ikizawa, Koichi Sasaki, Eiji Utsugi, Teruhiro Sci Rep Article Cancer peptide vaccines are a promising cancer immunotherapy that can induce cancer-specific cytotoxic T lymphocytes (CTLs) in tumors. However, recent clinical trials of cancer vaccines have revealed that the efficacy of the vaccines is limited. Targeting single antigens and vaccination with short peptides are partly the cause of the poor clinical outcomes. We synthesized a novel multi-epitope long peptide, TAS0314, which induced multiple epitope-specific CTLs in HLA knock-in mice. It also showed superior epitope-specific CTL induction and antitumor activity. We also established a combination treatment model of vaccination with PD-1/PD-L1 blockade in HLA-A*2402 knock-in mice, and it showed a synergistic antitumor effect with TAS0314. Thus, our data indicated that TAS0314 treatment, especially in combination with PD-1/PD-L1 blockade, is a promising therapeutic candidate for cancer immunotherapy. Nature Publishing Group UK 2020-10-14 /pmc/articles/PMC7560884/ /pubmed/33057061 http://dx.doi.org/10.1038/s41598-020-74187-6 Text en © The Author(s) 2020, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tanaka, Yuki Wada, Hiroshi Goto, Risa Osada, Toshihiro Yamamura, Keisuke Fukaya, Satoshi Shimizu, Atsushi Okubo, Mitsuru Minamiguchi, Kazuhisa Ikizawa, Koichi Sasaki, Eiji Utsugi, Teruhiro TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice |
title | TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice |
title_full | TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice |
title_fullStr | TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice |
title_full_unstemmed | TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice |
title_short | TAS0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with PD-1/PD-L1 blockade in HLA-A*2402 mice |
title_sort | tas0314, a novel multi-epitope long peptide vaccine, showed synergistic antitumor immunity with pd-1/pd-l1 blockade in hla-a*2402 mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560884/ https://www.ncbi.nlm.nih.gov/pubmed/33057061 http://dx.doi.org/10.1038/s41598-020-74187-6 |
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