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Recent advances in CAR-T cell engineering
Chimeric antigen receptor T (CAR-T) cell therapy is regarded as an effective solution for relapsed or refractory tumors, particularly for hematological malignancies. Although the initially approved anti-CD19 CAR-T therapy has produced impressive outcomes, setbacks such as high relapse rates and resi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333410/ https://www.ncbi.nlm.nih.gov/pubmed/32616000 http://dx.doi.org/10.1186/s13045-020-00910-5 |
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author | Huang, Ruihao Li, Xiaoping He, Yundi Zhu, Wen Gao, Lei Liu, Yao Gao, Li Wen, Qin Zhong, Jiang F. Zhang, Cheng Zhang, Xi |
author_facet | Huang, Ruihao Li, Xiaoping He, Yundi Zhu, Wen Gao, Lei Liu, Yao Gao, Li Wen, Qin Zhong, Jiang F. Zhang, Cheng Zhang, Xi |
author_sort | Huang, Ruihao |
collection | PubMed |
description | Chimeric antigen receptor T (CAR-T) cell therapy is regarded as an effective solution for relapsed or refractory tumors, particularly for hematological malignancies. Although the initially approved anti-CD19 CAR-T therapy has produced impressive outcomes, setbacks such as high relapse rates and resistance were experienced, driving the need to discover engineered CAR-T cells that are more effective for therapeutic use. Innovations in the structure and manufacturing of CAR-T cells have resulted in significant improvements in efficacy and persistence, particularly with the development of fourth-generation CAR-T cells. Paired with an immune modifier, the use of fourth-generation and next-generation CAR-T cells will not be limited because of cytotoxic effects and will be an efficient tool for overcoming the tumor microenvironment. In this review, we summarize the recent transformations in the ectodomain, transmembrane domain, and endodomain of the CAR structure, which, together with innovative manufacturing technology and improved cell sources, improve the prospects for the future development of CAR-T cell therapy. |
format | Online Article Text |
id | pubmed-7333410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73334102020-07-06 Recent advances in CAR-T cell engineering Huang, Ruihao Li, Xiaoping He, Yundi Zhu, Wen Gao, Lei Liu, Yao Gao, Li Wen, Qin Zhong, Jiang F. Zhang, Cheng Zhang, Xi J Hematol Oncol Review Chimeric antigen receptor T (CAR-T) cell therapy is regarded as an effective solution for relapsed or refractory tumors, particularly for hematological malignancies. Although the initially approved anti-CD19 CAR-T therapy has produced impressive outcomes, setbacks such as high relapse rates and resistance were experienced, driving the need to discover engineered CAR-T cells that are more effective for therapeutic use. Innovations in the structure and manufacturing of CAR-T cells have resulted in significant improvements in efficacy and persistence, particularly with the development of fourth-generation CAR-T cells. Paired with an immune modifier, the use of fourth-generation and next-generation CAR-T cells will not be limited because of cytotoxic effects and will be an efficient tool for overcoming the tumor microenvironment. In this review, we summarize the recent transformations in the ectodomain, transmembrane domain, and endodomain of the CAR structure, which, together with innovative manufacturing technology and improved cell sources, improve the prospects for the future development of CAR-T cell therapy. BioMed Central 2020-07-02 /pmc/articles/PMC7333410/ /pubmed/32616000 http://dx.doi.org/10.1186/s13045-020-00910-5 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Huang, Ruihao Li, Xiaoping He, Yundi Zhu, Wen Gao, Lei Liu, Yao Gao, Li Wen, Qin Zhong, Jiang F. Zhang, Cheng Zhang, Xi Recent advances in CAR-T cell engineering |
title | Recent advances in CAR-T cell engineering |
title_full | Recent advances in CAR-T cell engineering |
title_fullStr | Recent advances in CAR-T cell engineering |
title_full_unstemmed | Recent advances in CAR-T cell engineering |
title_short | Recent advances in CAR-T cell engineering |
title_sort | recent advances in car-t cell engineering |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333410/ https://www.ncbi.nlm.nih.gov/pubmed/32616000 http://dx.doi.org/10.1186/s13045-020-00910-5 |
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