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An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells
In T cell-based cancer immunotherapy, tumor antigen (Ag)-specific CD8(+) cytotoxic T lymphocytes (CTLs) can specifically target tumor Ags on malignant cells. This promising approach drove us to adopt this strategy of T cell transfer (ACT)-based immunotherapy for chronic viral infections. Here, we de...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806515/ https://www.ncbi.nlm.nih.gov/pubmed/33490980 http://dx.doi.org/10.1016/j.xpro.2020.100264 |
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author | Haque, Mohammad Xiong, Xiaofang Lei, Fengyang Das, Jugal Kishore Song, Jianxun |
author_facet | Haque, Mohammad Xiong, Xiaofang Lei, Fengyang Das, Jugal Kishore Song, Jianxun |
author_sort | Haque, Mohammad |
collection | PubMed |
description | In T cell-based cancer immunotherapy, tumor antigen (Ag)-specific CD8(+) cytotoxic T lymphocytes (CTLs) can specifically target tumor Ags on malignant cells. This promising approach drove us to adopt this strategy of T cell transfer (ACT)-based immunotherapy for chronic viral infections. Here, we describe the generation of hepatitis B virus (HBV) Ag-specific CTLs from induced pluripotent stem cells (iPSCs), i.e., iPSC-CTLs. Ag-specific iPSC-CTLs can target HBV Ag(+) cells and infiltrate into the liver to suppress HBV replication in a murine model. For complete details on the use and execution of this protocol, please refer to Haque et al. (2020). |
format | Online Article Text |
id | pubmed-7806515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78065152021-01-22 An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells Haque, Mohammad Xiong, Xiaofang Lei, Fengyang Das, Jugal Kishore Song, Jianxun STAR Protoc Protocol In T cell-based cancer immunotherapy, tumor antigen (Ag)-specific CD8(+) cytotoxic T lymphocytes (CTLs) can specifically target tumor Ags on malignant cells. This promising approach drove us to adopt this strategy of T cell transfer (ACT)-based immunotherapy for chronic viral infections. Here, we describe the generation of hepatitis B virus (HBV) Ag-specific CTLs from induced pluripotent stem cells (iPSCs), i.e., iPSC-CTLs. Ag-specific iPSC-CTLs can target HBV Ag(+) cells and infiltrate into the liver to suppress HBV replication in a murine model. For complete details on the use and execution of this protocol, please refer to Haque et al. (2020). Elsevier 2021-01-12 /pmc/articles/PMC7806515/ /pubmed/33490980 http://dx.doi.org/10.1016/j.xpro.2020.100264 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Haque, Mohammad Xiong, Xiaofang Lei, Fengyang Das, Jugal Kishore Song, Jianxun An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells |
title | An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells |
title_full | An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells |
title_fullStr | An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells |
title_full_unstemmed | An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells |
title_short | An optimized protocol for the generation of HBV viral antigen-specific T lymphocytes from pluripotent stem cells |
title_sort | optimized protocol for the generation of hbv viral antigen-specific t lymphocytes from pluripotent stem cells |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806515/ https://www.ncbi.nlm.nih.gov/pubmed/33490980 http://dx.doi.org/10.1016/j.xpro.2020.100264 |
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