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Article: The Epitope Basis of Embryonic Stem Cell-Induced Antitumor Immunity against Bladder Cancer

TitleThe Epitope Basis of Embryonic Stem Cell-Induced Antitumor Immunity against Bladder Cancer
Authors
Keywordsembryonic stem cells
epitopes
tumor immunity
vaccines
Issue Date12-Dec-2022
PublisherWiley
Citation
Advanced Healthcare Materials, 2022, v. 12, n. 9 How to Cite?
Abstract

Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) share many cellular and molecular features with cancer cells. Taking advantage of these similarities, stem cells are effective vaccines against cancers in animal models. However, the molecular basis is not well understood, which hinders the development of effective cancer vaccines. Here, prophylactic and therapeutic bladder cancer vaccines composed of allogeneic ESCs and CpG with or without granulocyte macrophage colony stimulating factor are tested. The ESC-based cancer vaccines are able to induce specific antitumor immunity including stimulating cytotoxic CD8+ T cells and memory CD4+ T cells, reducing myeloid-derived suppressor cells, and preventing bladder cancer growth in mouse models. Furthermore, several genes that are overexpressed in both ESCs and tumors are identified. An epitope-based vaccine designed with shared overexpressed proteins induces specific antitumor immunity and reduces bladder cancer growth. Functional epitopes underlying the action of stem cell-based vaccines against bladder cancer are identified and it is confirmed that ESC-based anticancer vaccines have great potential. A systematic approach is provided here to developing novel effective epitope-based cancer vaccines in the future.


Persistent Identifierhttp://hdl.handle.net/10722/356366
ISSN
2023 Impact Factor: 10.0
2023 SCImago Journal Rankings: 2.337
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorJin, Meiling-
dc.contributor.authorHu, Jingchu-
dc.contributor.authorTong, Lili-
dc.contributor.authorZhang, Bao Zhong-
dc.contributor.authorHuang, Jian Dong-
dc.date.accessioned2025-05-30T00:35:25Z-
dc.date.available2025-05-30T00:35:25Z-
dc.date.issued2022-12-12-
dc.identifier.citationAdvanced Healthcare Materials, 2022, v. 12, n. 9-
dc.identifier.issn2192-2640-
dc.identifier.urihttp://hdl.handle.net/10722/356366-
dc.description.abstract<p>Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) share many cellular and molecular features with cancer cells. Taking advantage of these similarities, stem cells are effective vaccines against cancers in animal models. However, the molecular basis is not well understood, which hinders the development of effective cancer vaccines. Here, prophylactic and therapeutic bladder cancer vaccines composed of allogeneic ESCs and CpG with or without granulocyte macrophage colony stimulating factor are tested. The ESC-based cancer vaccines are able to induce specific antitumor immunity including stimulating cytotoxic CD8+ T cells and memory CD4+ T cells, reducing myeloid-derived suppressor cells, and preventing bladder cancer growth in mouse models. Furthermore, several genes that are overexpressed in both ESCs and tumors are identified. An epitope-based vaccine designed with shared overexpressed proteins induces specific antitumor immunity and reduces bladder cancer growth. Functional epitopes underlying the action of stem cell-based vaccines against bladder cancer are identified and it is confirmed that ESC-based anticancer vaccines have great potential. A systematic approach is provided here to developing novel effective epitope-based cancer vaccines in the future.</p>-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofAdvanced Healthcare Materials-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectembryonic stem cells-
dc.subjectepitopes-
dc.subjecttumor immunity-
dc.subjectvaccines-
dc.titleThe Epitope Basis of Embryonic Stem Cell-Induced Antitumor Immunity against Bladder Cancer-
dc.typeArticle-
dc.identifier.doi10.1002/adhm.202202691-
dc.identifier.pmid36510117-
dc.identifier.scopuseid_2-s2.0-85145068614-
dc.identifier.volume12-
dc.identifier.issue9-
dc.identifier.eissn2192-2659-
dc.identifier.isiWOS:000901405600001-
dc.identifier.issnl2192-2640-

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