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Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges
Adoptive cell therapy using T cell receptor-engineered T cells (TCR-T) is a promising approach for cancer therapy with an expectation of no significant side effects. In the human body, mature T cells are armed with an incredible diversity of T cell receptors (TCRs) that theoretically react to the va...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690996/ https://www.ncbi.nlm.nih.gov/pubmed/38037114 http://dx.doi.org/10.1186/s40364-023-00534-0 |
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author | Pang, Zhi Lu, Man-man Zhang, Yu Gao, Yuan Bai, Jin-jin Gu, Jian-ying Xie, Lu Wu, Wei-zhong |
author_facet | Pang, Zhi Lu, Man-man Zhang, Yu Gao, Yuan Bai, Jin-jin Gu, Jian-ying Xie, Lu Wu, Wei-zhong |
author_sort | Pang, Zhi |
collection | PubMed |
description | Adoptive cell therapy using T cell receptor-engineered T cells (TCR-T) is a promising approach for cancer therapy with an expectation of no significant side effects. In the human body, mature T cells are armed with an incredible diversity of T cell receptors (TCRs) that theoretically react to the variety of random mutations generated by tumor cells. The outcomes, however, of current clinical trials using TCR-T cell therapies are not very successful especially involving solid tumors. The therapy still faces numerous challenges in the efficient screening of tumor-specific antigens and their cognate TCRs. In this review, we first introduce TCR structure-based antigen recognition and signaling, then describe recent advances in neoantigens and their specific TCR screening technologies, and finally summarize ongoing clinical trials of TCR-T therapies against neoantigens. More importantly, we also present the current challenges of TCR-T cell-based immunotherapies, e.g., the safety of viral vectors, the mismatch of T cell receptor, the impediment of suppressive tumor microenvironment. Finally, we highlight new insights and directions for personalized TCR-T therapy. |
format | Online Article Text |
id | pubmed-10690996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106909962023-12-02 Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges Pang, Zhi Lu, Man-man Zhang, Yu Gao, Yuan Bai, Jin-jin Gu, Jian-ying Xie, Lu Wu, Wei-zhong Biomark Res Review Adoptive cell therapy using T cell receptor-engineered T cells (TCR-T) is a promising approach for cancer therapy with an expectation of no significant side effects. In the human body, mature T cells are armed with an incredible diversity of T cell receptors (TCRs) that theoretically react to the variety of random mutations generated by tumor cells. The outcomes, however, of current clinical trials using TCR-T cell therapies are not very successful especially involving solid tumors. The therapy still faces numerous challenges in the efficient screening of tumor-specific antigens and their cognate TCRs. In this review, we first introduce TCR structure-based antigen recognition and signaling, then describe recent advances in neoantigens and their specific TCR screening technologies, and finally summarize ongoing clinical trials of TCR-T therapies against neoantigens. More importantly, we also present the current challenges of TCR-T cell-based immunotherapies, e.g., the safety of viral vectors, the mismatch of T cell receptor, the impediment of suppressive tumor microenvironment. Finally, we highlight new insights and directions for personalized TCR-T therapy. BioMed Central 2023-12-01 /pmc/articles/PMC10690996/ /pubmed/38037114 http://dx.doi.org/10.1186/s40364-023-00534-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Pang, Zhi Lu, Man-man Zhang, Yu Gao, Yuan Bai, Jin-jin Gu, Jian-ying Xie, Lu Wu, Wei-zhong Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges |
title | Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges |
title_full | Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges |
title_fullStr | Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges |
title_full_unstemmed | Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges |
title_short | Neoantigen-targeted TCR-engineered T cell immunotherapy: current advances and challenges |
title_sort | neoantigen-targeted tcr-engineered t cell immunotherapy: current advances and challenges |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690996/ https://www.ncbi.nlm.nih.gov/pubmed/38037114 http://dx.doi.org/10.1186/s40364-023-00534-0 |
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