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Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells
Adoptive cell therapy (ACT) has seen a steep rise of new therapeutic approaches in its immune-oncology pipeline over the last years. This is in great part due to the recent approvals of chimeric antigen receptor (CAR)-T cell therapies and their remarkable efficacy in certain soluble tumors. A big fo...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025359/ https://www.ncbi.nlm.nih.gov/pubmed/36949949 http://dx.doi.org/10.3389/fimmu.2023.1121030 |
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author | Hiltensperger, Michael Krackhardt, Angela M. |
author_facet | Hiltensperger, Michael Krackhardt, Angela M. |
author_sort | Hiltensperger, Michael |
collection | PubMed |
description | Adoptive cell therapy (ACT) has seen a steep rise of new therapeutic approaches in its immune-oncology pipeline over the last years. This is in great part due to the recent approvals of chimeric antigen receptor (CAR)-T cell therapies and their remarkable efficacy in certain soluble tumors. A big focus of ACT lies on T cells and how to genetically modify them to target and kill tumor cells. Genetically modified T cells that are currently utilized are either equipped with an engineered CAR or a T cell receptor (TCR) for this purpose. Both strategies have their advantages and limitations. While CAR-T cell therapies are already used in the clinic, these therapies face challenges when it comes to the treatment of solid tumors. New designs of next-generation CAR-T cells might be able to overcome these hurdles. Moreover, CARs are restricted to surface antigens. Genetically engineered TCR-T cells targeting intracellular antigens might provide necessary qualities for the treatment of solid tumors. In this review, we will summarize the major advancements of the CAR-T and TCR-T cell technology. Moreover, we will cover ongoing clinical trials, discuss current challenges, and provide an assessment of future directions within the field. |
format | Online Article Text |
id | pubmed-10025359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100253592023-03-21 Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells Hiltensperger, Michael Krackhardt, Angela M. Front Immunol Immunology Adoptive cell therapy (ACT) has seen a steep rise of new therapeutic approaches in its immune-oncology pipeline over the last years. This is in great part due to the recent approvals of chimeric antigen receptor (CAR)-T cell therapies and their remarkable efficacy in certain soluble tumors. A big focus of ACT lies on T cells and how to genetically modify them to target and kill tumor cells. Genetically modified T cells that are currently utilized are either equipped with an engineered CAR or a T cell receptor (TCR) for this purpose. Both strategies have their advantages and limitations. While CAR-T cell therapies are already used in the clinic, these therapies face challenges when it comes to the treatment of solid tumors. New designs of next-generation CAR-T cells might be able to overcome these hurdles. Moreover, CARs are restricted to surface antigens. Genetically engineered TCR-T cells targeting intracellular antigens might provide necessary qualities for the treatment of solid tumors. In this review, we will summarize the major advancements of the CAR-T and TCR-T cell technology. Moreover, we will cover ongoing clinical trials, discuss current challenges, and provide an assessment of future directions within the field. Frontiers Media S.A. 2023-03-06 /pmc/articles/PMC10025359/ /pubmed/36949949 http://dx.doi.org/10.3389/fimmu.2023.1121030 Text en Copyright © 2023 Hiltensperger and Krackhardt https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Hiltensperger, Michael Krackhardt, Angela M. Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells |
title | Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells |
title_full | Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells |
title_fullStr | Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells |
title_full_unstemmed | Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells |
title_short | Current and future concepts for the generation and application of genetically engineered CAR-T and TCR-T cells |
title_sort | current and future concepts for the generation and application of genetically engineered car-t and tcr-t cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025359/ https://www.ncbi.nlm.nih.gov/pubmed/36949949 http://dx.doi.org/10.3389/fimmu.2023.1121030 |
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