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Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor

T cell receptor‐engineered T (TCR‐T) cell therapy has demonstrated therapeutic effects in basic research and clinical trials for treating solid tumors. Due to the peptide‐dependent recognition and the human leukocyte antigen (HLA)‐restriction, TCR‐T cell therapy is generally custom designed to targe...

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Autores principales: Xu, Ruihan, Wang, Qin, Zhu, Junmeng, Bei, Yuncheng, Chu, Yanhong, Sun, Zhichen, Du, Shiyao, Zhou, Shujuan, Ding, Naiqing, Meng, Fanyan, Liu, Baorui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658479/
https://www.ncbi.nlm.nih.gov/pubmed/38023696
http://dx.doi.org/10.1002/btm2.10585
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author Xu, Ruihan
Wang, Qin
Zhu, Junmeng
Bei, Yuncheng
Chu, Yanhong
Sun, Zhichen
Du, Shiyao
Zhou, Shujuan
Ding, Naiqing
Meng, Fanyan
Liu, Baorui
author_facet Xu, Ruihan
Wang, Qin
Zhu, Junmeng
Bei, Yuncheng
Chu, Yanhong
Sun, Zhichen
Du, Shiyao
Zhou, Shujuan
Ding, Naiqing
Meng, Fanyan
Liu, Baorui
author_sort Xu, Ruihan
collection PubMed
description T cell receptor‐engineered T (TCR‐T) cell therapy has demonstrated therapeutic effects in basic research and clinical trials for treating solid tumors. Due to the peptide‐dependent recognition and the human leukocyte antigen (HLA)‐restriction, TCR‐T cell therapy is generally custom designed to target individual antigens. The lack of suitable universal targets for tumor cells significantly limits its clinical applications. Establishing a universal TCR‐T treatment strategy is of great significance. This study designed and evaluated the HLA‐peptide‐addressing universal (HAUL) TCR‐T cell therapy based on HLA‐peptide (pHLA) loaded membrance fusogenic deliver system. The pHLA‐NP‐based tumor cell membrane modification technology can transfer the pHLA onto the surface of tumor cells through membrane fusogenic nanoparticles. Then tumor cells are recognized and killed by TCR‐T cells specifically. The HAUL TCR‐T cell therapy technology is a universal technology that enables tumor cells to be identified and killed by specific TCR‐T cells, regardless of the HLA typing of tumor cells.
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spelling pubmed-106584792023-08-07 Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor Xu, Ruihan Wang, Qin Zhu, Junmeng Bei, Yuncheng Chu, Yanhong Sun, Zhichen Du, Shiyao Zhou, Shujuan Ding, Naiqing Meng, Fanyan Liu, Baorui Bioeng Transl Med Regular Issue Articles T cell receptor‐engineered T (TCR‐T) cell therapy has demonstrated therapeutic effects in basic research and clinical trials for treating solid tumors. Due to the peptide‐dependent recognition and the human leukocyte antigen (HLA)‐restriction, TCR‐T cell therapy is generally custom designed to target individual antigens. The lack of suitable universal targets for tumor cells significantly limits its clinical applications. Establishing a universal TCR‐T treatment strategy is of great significance. This study designed and evaluated the HLA‐peptide‐addressing universal (HAUL) TCR‐T cell therapy based on HLA‐peptide (pHLA) loaded membrance fusogenic deliver system. The pHLA‐NP‐based tumor cell membrane modification technology can transfer the pHLA onto the surface of tumor cells through membrane fusogenic nanoparticles. Then tumor cells are recognized and killed by TCR‐T cells specifically. The HAUL TCR‐T cell therapy technology is a universal technology that enables tumor cells to be identified and killed by specific TCR‐T cells, regardless of the HLA typing of tumor cells. John Wiley & Sons, Inc. 2023-08-07 /pmc/articles/PMC10658479/ /pubmed/38023696 http://dx.doi.org/10.1002/btm2.10585 Text en © 2023 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Issue Articles
Xu, Ruihan
Wang, Qin
Zhu, Junmeng
Bei, Yuncheng
Chu, Yanhong
Sun, Zhichen
Du, Shiyao
Zhou, Shujuan
Ding, Naiqing
Meng, Fanyan
Liu, Baorui
Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor
title Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor
title_full Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor
title_fullStr Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor
title_full_unstemmed Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor
title_short Membrane fusogenic nanoparticle‐based HLA‐peptide‐addressing universal T cell receptor‐engineered T (HAUL TCR‐T) cell therapy in solid tumor
title_sort membrane fusogenic nanoparticle‐based hla‐peptide‐addressing universal t cell receptor‐engineered t (haul tcr‐t) cell therapy in solid tumor
topic Regular Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658479/
https://www.ncbi.nlm.nih.gov/pubmed/38023696
http://dx.doi.org/10.1002/btm2.10585
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