Potential and development of cellular vesicle vaccines in cancer immunotherapy

Abstract Cancer vaccines are promising as an effective means of stimulating the immune system to clear tumors as well as to establish immune surveillance. In this paper, we discuss the main platforms and current status of cancer vaccines and propose a new cancer vaccine platform, the cytosolic vesic...

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Main Authors: Wenxi Zhao, Xianjun Li, Jialu Guan, Shuai Yan, Lizhi Teng, Xitong Sun, Yuhan Dong, Hongyue Wang, Weiyang Tao
Format: Article
Language:English
Published: Springer 2025-01-01
Series:Discover Oncology
Subjects:
Online Access:https://doi.org/10.1007/s12672-025-01781-3
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author Wenxi Zhao
Xianjun Li
Jialu Guan
Shuai Yan
Lizhi Teng
Xitong Sun
Yuhan Dong
Hongyue Wang
Weiyang Tao
author_facet Wenxi Zhao
Xianjun Li
Jialu Guan
Shuai Yan
Lizhi Teng
Xitong Sun
Yuhan Dong
Hongyue Wang
Weiyang Tao
author_sort Wenxi Zhao
collection DOAJ
description Abstract Cancer vaccines are promising as an effective means of stimulating the immune system to clear tumors as well as to establish immune surveillance. In this paper, we discuss the main platforms and current status of cancer vaccines and propose a new cancer vaccine platform, the cytosolic vesicle vaccine. This vaccine has a unique structure that can integrate antigen and adjuvant carriers to improve the delivery efficiency and immune activation ability, which brings new ideas for cancer vaccine design. Tumor exosomes carry antigens and MHC-peptide complexes, which can provide tumor antigens to antigen-processing cells and increase the chances of recognition of tumor antigens by immune cells. DEVs play a role in amplifying the immune response by acting as carriers for the dissemination of antigenic substances in dendritic cells. OMVs, with their natural adjuvant properties, are one of the advantages for the preparation of antitumor vaccines. This paper presents the advantages of these three bacteria/extracellular vesicles as cancer vaccines and discusses the potential applications of functionally modified extracellular vesicles as cancer vaccines after cellular engineering or genetic engineering, as well as current clinical trials of extracellular vesicle vaccines. In summary, extracellular vesicle vaccines are a promising direction for cancer vaccine research.
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institution Kabale University
issn 2730-6011
language English
publishDate 2025-01-01
publisher Springer
record_format Article
series Discover Oncology
spelling doaj-art-f1eb4cf5037848b9a3787c2dcc9de8192025-01-19T12:29:09ZengSpringerDiscover Oncology2730-60112025-01-0116112210.1007/s12672-025-01781-3Potential and development of cellular vesicle vaccines in cancer immunotherapyWenxi Zhao0Xianjun Li1Jialu Guan2Shuai Yan3Lizhi Teng4Xitong Sun5Yuhan Dong6Hongyue Wang7Weiyang Tao8Department of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityDepartment of Breast Surgery, The First Affiliated Hospital of Harbin Medical UniversityAbstract Cancer vaccines are promising as an effective means of stimulating the immune system to clear tumors as well as to establish immune surveillance. In this paper, we discuss the main platforms and current status of cancer vaccines and propose a new cancer vaccine platform, the cytosolic vesicle vaccine. This vaccine has a unique structure that can integrate antigen and adjuvant carriers to improve the delivery efficiency and immune activation ability, which brings new ideas for cancer vaccine design. Tumor exosomes carry antigens and MHC-peptide complexes, which can provide tumor antigens to antigen-processing cells and increase the chances of recognition of tumor antigens by immune cells. DEVs play a role in amplifying the immune response by acting as carriers for the dissemination of antigenic substances in dendritic cells. OMVs, with their natural adjuvant properties, are one of the advantages for the preparation of antitumor vaccines. This paper presents the advantages of these three bacteria/extracellular vesicles as cancer vaccines and discusses the potential applications of functionally modified extracellular vesicles as cancer vaccines after cellular engineering or genetic engineering, as well as current clinical trials of extracellular vesicle vaccines. In summary, extracellular vesicle vaccines are a promising direction for cancer vaccine research.https://doi.org/10.1007/s12672-025-01781-3Cellular vesiclesCancer vaccineImmunotherapy
spellingShingle Wenxi Zhao
Xianjun Li
Jialu Guan
Shuai Yan
Lizhi Teng
Xitong Sun
Yuhan Dong
Hongyue Wang
Weiyang Tao
Potential and development of cellular vesicle vaccines in cancer immunotherapy
Discover Oncology
Cellular vesicles
Cancer vaccine
Immunotherapy
title Potential and development of cellular vesicle vaccines in cancer immunotherapy
title_full Potential and development of cellular vesicle vaccines in cancer immunotherapy
title_fullStr Potential and development of cellular vesicle vaccines in cancer immunotherapy
title_full_unstemmed Potential and development of cellular vesicle vaccines in cancer immunotherapy
title_short Potential and development of cellular vesicle vaccines in cancer immunotherapy
title_sort potential and development of cellular vesicle vaccines in cancer immunotherapy
topic Cellular vesicles
Cancer vaccine
Immunotherapy
url https://doi.org/10.1007/s12672-025-01781-3
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AT lizhiteng potentialanddevelopmentofcellularvesiclevaccinesincancerimmunotherapy
AT xitongsun potentialanddevelopmentofcellularvesiclevaccinesincancerimmunotherapy
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