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Engineering γδ T Cells: Recognizing and Activating on Their Own Way
Adoptive cell therapy (ACT) with engineered T cells has emerged as a promising strategy for the treatment of malignant tumors. Among them, there is great interest in engineered γδ T cells for ACT. With both adaptive and innate immune characteristics, γδ T cells can be activated by γδ TCRs to recogni...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120431/ https://www.ncbi.nlm.nih.gov/pubmed/35603176 http://dx.doi.org/10.3389/fimmu.2022.889051 |
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author | Dong, Ruoyu Zhang, Yixi Xiao, Haowen Zeng, Xun |
author_facet | Dong, Ruoyu Zhang, Yixi Xiao, Haowen Zeng, Xun |
author_sort | Dong, Ruoyu |
collection | PubMed |
description | Adoptive cell therapy (ACT) with engineered T cells has emerged as a promising strategy for the treatment of malignant tumors. Among them, there is great interest in engineered γδ T cells for ACT. With both adaptive and innate immune characteristics, γδ T cells can be activated by γδ TCRs to recognize antigens in a MHC-independent manner, or by NK receptors to recognize stress-induced molecules. The dual recognition system enables γδ T cells with unique activation and cytotoxicity profiles, which should be considered for the design of engineered γδ T cells. However, the current designs of engineered γδ T cells mostly follow the strategies that used in αβ T cells, but not making good use of the specific characteristics of γδ T cells. Therefore, it is no surprising that current engineered γδ T cells in preclinical or clinical trials have limited efficacy. In this review, we summarized the patterns of antigen recognition of γδ T cells and the features of signaling pathways for the functions of γδ T cells. This review will additionally discuss current progress in engineered γδ T cells and provide insights in the design of engineered γδ T cells based on their specific characteristics. |
format | Online Article Text |
id | pubmed-9120431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91204312022-05-21 Engineering γδ T Cells: Recognizing and Activating on Their Own Way Dong, Ruoyu Zhang, Yixi Xiao, Haowen Zeng, Xun Front Immunol Immunology Adoptive cell therapy (ACT) with engineered T cells has emerged as a promising strategy for the treatment of malignant tumors. Among them, there is great interest in engineered γδ T cells for ACT. With both adaptive and innate immune characteristics, γδ T cells can be activated by γδ TCRs to recognize antigens in a MHC-independent manner, or by NK receptors to recognize stress-induced molecules. The dual recognition system enables γδ T cells with unique activation and cytotoxicity profiles, which should be considered for the design of engineered γδ T cells. However, the current designs of engineered γδ T cells mostly follow the strategies that used in αβ T cells, but not making good use of the specific characteristics of γδ T cells. Therefore, it is no surprising that current engineered γδ T cells in preclinical or clinical trials have limited efficacy. In this review, we summarized the patterns of antigen recognition of γδ T cells and the features of signaling pathways for the functions of γδ T cells. This review will additionally discuss current progress in engineered γδ T cells and provide insights in the design of engineered γδ T cells based on their specific characteristics. Frontiers Media S.A. 2022-05-06 /pmc/articles/PMC9120431/ /pubmed/35603176 http://dx.doi.org/10.3389/fimmu.2022.889051 Text en Copyright © 2022 Dong, Zhang, Xiao and Zeng 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 Dong, Ruoyu Zhang, Yixi Xiao, Haowen Zeng, Xun Engineering γδ T Cells: Recognizing and Activating on Their Own Way |
title | Engineering γδ T Cells: Recognizing and Activating on Their Own Way |
title_full | Engineering γδ T Cells: Recognizing and Activating on Their Own Way |
title_fullStr | Engineering γδ T Cells: Recognizing and Activating on Their Own Way |
title_full_unstemmed | Engineering γδ T Cells: Recognizing and Activating on Their Own Way |
title_short | Engineering γδ T Cells: Recognizing and Activating on Their Own Way |
title_sort | engineering γδ t cells: recognizing and activating on their own way |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120431/ https://www.ncbi.nlm.nih.gov/pubmed/35603176 http://dx.doi.org/10.3389/fimmu.2022.889051 |
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