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Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma
The adoptive transfer of naturally occurring T cells that recognize cancer neoantigens has led to durable tumor regressions in select patients with cancer. However, it remains unknown whether such T cells can be isolated from and used to treat patients with glioblastoma, a cancer that is refractory...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286793/ https://www.ncbi.nlm.nih.gov/pubmed/34266885 http://dx.doi.org/10.1136/jitc-2021-002882 |
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author | Leko, Vid Cafri, Gal Yossef, Rami Paria, Biman Hill, Victoria Gurusamy, Devikala Zheng, Zhili Gartner, Jared J Prickett, Todd D Goff, Stephanie L Robbins, Paul Lu, Yong-Chen Rosenberg, Steven A |
author_facet | Leko, Vid Cafri, Gal Yossef, Rami Paria, Biman Hill, Victoria Gurusamy, Devikala Zheng, Zhili Gartner, Jared J Prickett, Todd D Goff, Stephanie L Robbins, Paul Lu, Yong-Chen Rosenberg, Steven A |
author_sort | Leko, Vid |
collection | PubMed |
description | The adoptive transfer of naturally occurring T cells that recognize cancer neoantigens has led to durable tumor regressions in select patients with cancer. However, it remains unknown whether such T cells can be isolated from and used to treat patients with glioblastoma, a cancer that is refractory to currently available therapies. To answer this question, we stimulated patient blood-derived memory T cells in vitro using peptides and minigenes that represented point mutations unique to patients’ tumors (ie, candidate neoantigens) and then tested their ability to specifically recognize these mutations. In a cohort of five patients with glioblastoma, we found that circulating CD4(+) memory T cells from one patient recognized a cancer neoantigen harboring a mutation in the EED gene (EED(H189N)) that was unique to that patient’s tumor. This finding suggests that neoantigen-reactive T cells could indeed be isolated from patients with glioblastoma, thereby providing a rationale for further efforts to develop neoantigen-directed adoptive T cell therapy for this disease. |
format | Online Article Text |
id | pubmed-8286793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-82867932021-07-30 Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma Leko, Vid Cafri, Gal Yossef, Rami Paria, Biman Hill, Victoria Gurusamy, Devikala Zheng, Zhili Gartner, Jared J Prickett, Todd D Goff, Stephanie L Robbins, Paul Lu, Yong-Chen Rosenberg, Steven A J Immunother Cancer Immune Cell Therapies and Immune Cell Engineering The adoptive transfer of naturally occurring T cells that recognize cancer neoantigens has led to durable tumor regressions in select patients with cancer. However, it remains unknown whether such T cells can be isolated from and used to treat patients with glioblastoma, a cancer that is refractory to currently available therapies. To answer this question, we stimulated patient blood-derived memory T cells in vitro using peptides and minigenes that represented point mutations unique to patients’ tumors (ie, candidate neoantigens) and then tested their ability to specifically recognize these mutations. In a cohort of five patients with glioblastoma, we found that circulating CD4(+) memory T cells from one patient recognized a cancer neoantigen harboring a mutation in the EED gene (EED(H189N)) that was unique to that patient’s tumor. This finding suggests that neoantigen-reactive T cells could indeed be isolated from patients with glioblastoma, thereby providing a rationale for further efforts to develop neoantigen-directed adoptive T cell therapy for this disease. BMJ Publishing Group 2021-07-15 /pmc/articles/PMC8286793/ /pubmed/34266885 http://dx.doi.org/10.1136/jitc-2021-002882 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Immune Cell Therapies and Immune Cell Engineering Leko, Vid Cafri, Gal Yossef, Rami Paria, Biman Hill, Victoria Gurusamy, Devikala Zheng, Zhili Gartner, Jared J Prickett, Todd D Goff, Stephanie L Robbins, Paul Lu, Yong-Chen Rosenberg, Steven A Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma |
title | Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma |
title_full | Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma |
title_fullStr | Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma |
title_full_unstemmed | Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma |
title_short | Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma |
title_sort | identification of neoantigen-reactive t lymphocytes in the peripheral blood of a patient with glioblastoma |
topic | Immune Cell Therapies and Immune Cell Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286793/ https://www.ncbi.nlm.nih.gov/pubmed/34266885 http://dx.doi.org/10.1136/jitc-2021-002882 |
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