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Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors
For effective targeted therapy of cancer with chemotherapy-loaded nanoparticles (NPs), antigens that are selective for cancer cells should be targeted to minimise off-tumour toxicity. Human leukocyte antigens (HLAs) are attractive cancer targets as they can present peptides from tumour-selective pro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447836/ https://www.ncbi.nlm.nih.gov/pubmed/34533174 http://dx.doi.org/10.1039/d1nr04001d |
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author | McDaid, William J. Lissin, Nikolai Pollheimer, Ellen Greene, Michelle Leach, Adam Smyth, Peter Bossi, Giovanna Longley, Daniel Cole, David K. Scott, Christopher J. |
author_facet | McDaid, William J. Lissin, Nikolai Pollheimer, Ellen Greene, Michelle Leach, Adam Smyth, Peter Bossi, Giovanna Longley, Daniel Cole, David K. Scott, Christopher J. |
author_sort | McDaid, William J. |
collection | PubMed |
description | For effective targeted therapy of cancer with chemotherapy-loaded nanoparticles (NPs), antigens that are selective for cancer cells should be targeted to minimise off-tumour toxicity. Human leukocyte antigens (HLAs) are attractive cancer targets as they can present peptides from tumour-selective proteins on the cell surface, which can be recognised by T cells via T cell receptors (TCRs). In this study, docetaxel-loaded polymeric NPs were conjugated to recombinant affinity-enhanced TCRs to target breast cancer cells presenting a tumour-selective peptide-HLA complex. The TCR-conjugated nanoparticles enabled enhanced delivery of docetaxel and induced cell death through tumour-specific peptide-HLA targeting. These in vitro data demonstrate the potential of targeting tumour-restricted peptide-HLA epitopes using high affinity TCR-conjugated nanoparticles, representing a novel treatment strategy to deliver therapeutic drugs specifically to cancer cells. |
format | Online Article Text |
id | pubmed-8447836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-84478362021-10-18 Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors McDaid, William J. Lissin, Nikolai Pollheimer, Ellen Greene, Michelle Leach, Adam Smyth, Peter Bossi, Giovanna Longley, Daniel Cole, David K. Scott, Christopher J. Nanoscale Chemistry For effective targeted therapy of cancer with chemotherapy-loaded nanoparticles (NPs), antigens that are selective for cancer cells should be targeted to minimise off-tumour toxicity. Human leukocyte antigens (HLAs) are attractive cancer targets as they can present peptides from tumour-selective proteins on the cell surface, which can be recognised by T cells via T cell receptors (TCRs). In this study, docetaxel-loaded polymeric NPs were conjugated to recombinant affinity-enhanced TCRs to target breast cancer cells presenting a tumour-selective peptide-HLA complex. The TCR-conjugated nanoparticles enabled enhanced delivery of docetaxel and induced cell death through tumour-specific peptide-HLA targeting. These in vitro data demonstrate the potential of targeting tumour-restricted peptide-HLA epitopes using high affinity TCR-conjugated nanoparticles, representing a novel treatment strategy to deliver therapeutic drugs specifically to cancer cells. The Royal Society of Chemistry 2021-08-20 /pmc/articles/PMC8447836/ /pubmed/34533174 http://dx.doi.org/10.1039/d1nr04001d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry McDaid, William J. Lissin, Nikolai Pollheimer, Ellen Greene, Michelle Leach, Adam Smyth, Peter Bossi, Giovanna Longley, Daniel Cole, David K. Scott, Christopher J. Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors |
title | Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors |
title_full | Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors |
title_fullStr | Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors |
title_full_unstemmed | Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors |
title_short | Enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered T cell receptors |
title_sort | enhanced target-specific delivery of docetaxel-loaded nanoparticles using engineered t cell receptors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447836/ https://www.ncbi.nlm.nih.gov/pubmed/34533174 http://dx.doi.org/10.1039/d1nr04001d |
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