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CAR-T cell potency: from structural elements to vector backbone components
Chimeric antigen receptor (CAR) T cell therapy, in which a patient’s own T lymphocytes are engineered to recognize and kill cancer cells, has achieved remarkable success in some hematological malignancies in preclinical and clinical trials, resulting in six FDA-approved CAR-T products currently avai...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487061/ https://www.ncbi.nlm.nih.gov/pubmed/36123710 http://dx.doi.org/10.1186/s40364-022-00417-w |
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author | Mazinani, Marzieh Rahbarizadeh, Fatemeh |
author_facet | Mazinani, Marzieh Rahbarizadeh, Fatemeh |
author_sort | Mazinani, Marzieh |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T cell therapy, in which a patient’s own T lymphocytes are engineered to recognize and kill cancer cells, has achieved remarkable success in some hematological malignancies in preclinical and clinical trials, resulting in six FDA-approved CAR-T products currently available in the market. Once equipped with a CAR construct, T cells act as living drugs and recognize and eliminate the target tumor cells in an MHC-independent manner. In this review, we first described all structural modular of CAR in detail, focusing on more recent findings. We then pointed out behind-the-scene elements contributing to CAR expression and reviewed how CAR expression can be drastically affected by the elements embedded in the viral vector backbone. |
format | Online Article Text |
id | pubmed-9487061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94870612022-09-21 CAR-T cell potency: from structural elements to vector backbone components Mazinani, Marzieh Rahbarizadeh, Fatemeh Biomark Res Review Chimeric antigen receptor (CAR) T cell therapy, in which a patient’s own T lymphocytes are engineered to recognize and kill cancer cells, has achieved remarkable success in some hematological malignancies in preclinical and clinical trials, resulting in six FDA-approved CAR-T products currently available in the market. Once equipped with a CAR construct, T cells act as living drugs and recognize and eliminate the target tumor cells in an MHC-independent manner. In this review, we first described all structural modular of CAR in detail, focusing on more recent findings. We then pointed out behind-the-scene elements contributing to CAR expression and reviewed how CAR expression can be drastically affected by the elements embedded in the viral vector backbone. BioMed Central 2022-09-19 /pmc/articles/PMC9487061/ /pubmed/36123710 http://dx.doi.org/10.1186/s40364-022-00417-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Mazinani, Marzieh Rahbarizadeh, Fatemeh CAR-T cell potency: from structural elements to vector backbone components |
title | CAR-T cell potency: from structural elements to vector backbone components |
title_full | CAR-T cell potency: from structural elements to vector backbone components |
title_fullStr | CAR-T cell potency: from structural elements to vector backbone components |
title_full_unstemmed | CAR-T cell potency: from structural elements to vector backbone components |
title_short | CAR-T cell potency: from structural elements to vector backbone components |
title_sort | car-t cell potency: from structural elements to vector backbone components |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487061/ https://www.ncbi.nlm.nih.gov/pubmed/36123710 http://dx.doi.org/10.1186/s40364-022-00417-w |
work_keys_str_mv | AT mazinanimarzieh cartcellpotencyfromstructuralelementstovectorbackbonecomponents AT rahbarizadehfatemeh cartcellpotencyfromstructuralelementstovectorbackbonecomponents |