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TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs
T cell receptor (TCR) technologies, including repertoire analyses and T cell engineering, are increasingly important in the clinical management of cellular immunity in cancer, transplantation, and other immune diseases. However, sensitive and reliable methods for repertoire analyses and TCR cloning...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163020/ https://www.ncbi.nlm.nih.gov/pubmed/37159666 http://dx.doi.org/10.1016/j.crmeth.2023.100459 |
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author | Genolet, Raphael Bobisse, Sara Chiffelle, Johanna Arnaud, Marion Petremand, Rémy Queiroz, Lise Michel, Alexandra Reichenbach, Patrick Cesbron, Julien Auger, Aymeric Baumgaertner, Petra Guillaume, Philippe Schmidt, Julien Irving, Melita Kandalaft, Lana E. Speiser, Daniel E. Coukos, George Harari, Alexandre |
author_facet | Genolet, Raphael Bobisse, Sara Chiffelle, Johanna Arnaud, Marion Petremand, Rémy Queiroz, Lise Michel, Alexandra Reichenbach, Patrick Cesbron, Julien Auger, Aymeric Baumgaertner, Petra Guillaume, Philippe Schmidt, Julien Irving, Melita Kandalaft, Lana E. Speiser, Daniel E. Coukos, George Harari, Alexandre |
author_sort | Genolet, Raphael |
collection | PubMed |
description | T cell receptor (TCR) technologies, including repertoire analyses and T cell engineering, are increasingly important in the clinical management of cellular immunity in cancer, transplantation, and other immune diseases. However, sensitive and reliable methods for repertoire analyses and TCR cloning are still lacking. Here, we report on SEQTR, a high-throughput approach to analyze human and mouse repertoires that is more sensitive, reproducible, and accurate as compared with commonly used assays, and thus more reliably captures the complexity of blood and tumor TCR repertoires. We also present a TCR cloning strategy to specifically amplify TCRs from T cell populations. Positioned downstream of single-cell or bulk TCR sequencing, it allows time- and cost-effective discovery, cloning, screening, and engineering of tumor-specific TCRs. Together, these methods will accelerate TCR repertoire analyses in discovery, translational, and clinical settings and permit fast TCR engineering for cellular therapies. |
format | Online Article Text |
id | pubmed-10163020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101630202023-05-07 TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs Genolet, Raphael Bobisse, Sara Chiffelle, Johanna Arnaud, Marion Petremand, Rémy Queiroz, Lise Michel, Alexandra Reichenbach, Patrick Cesbron, Julien Auger, Aymeric Baumgaertner, Petra Guillaume, Philippe Schmidt, Julien Irving, Melita Kandalaft, Lana E. Speiser, Daniel E. Coukos, George Harari, Alexandre Cell Rep Methods Article T cell receptor (TCR) technologies, including repertoire analyses and T cell engineering, are increasingly important in the clinical management of cellular immunity in cancer, transplantation, and other immune diseases. However, sensitive and reliable methods for repertoire analyses and TCR cloning are still lacking. Here, we report on SEQTR, a high-throughput approach to analyze human and mouse repertoires that is more sensitive, reproducible, and accurate as compared with commonly used assays, and thus more reliably captures the complexity of blood and tumor TCR repertoires. We also present a TCR cloning strategy to specifically amplify TCRs from T cell populations. Positioned downstream of single-cell or bulk TCR sequencing, it allows time- and cost-effective discovery, cloning, screening, and engineering of tumor-specific TCRs. Together, these methods will accelerate TCR repertoire analyses in discovery, translational, and clinical settings and permit fast TCR engineering for cellular therapies. Elsevier 2023-04-24 /pmc/articles/PMC10163020/ /pubmed/37159666 http://dx.doi.org/10.1016/j.crmeth.2023.100459 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Genolet, Raphael Bobisse, Sara Chiffelle, Johanna Arnaud, Marion Petremand, Rémy Queiroz, Lise Michel, Alexandra Reichenbach, Patrick Cesbron, Julien Auger, Aymeric Baumgaertner, Petra Guillaume, Philippe Schmidt, Julien Irving, Melita Kandalaft, Lana E. Speiser, Daniel E. Coukos, George Harari, Alexandre TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs |
title | TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs |
title_full | TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs |
title_fullStr | TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs |
title_full_unstemmed | TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs |
title_short | TCR sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive TCRs |
title_sort | tcr sequencing and cloning methods for repertoire analysis and isolation of tumor-reactive tcrs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163020/ https://www.ncbi.nlm.nih.gov/pubmed/37159666 http://dx.doi.org/10.1016/j.crmeth.2023.100459 |
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