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Genetically enhanced T lymphocytes and the intensive care unit
Chimeric antigen receptor-modified T cells (CAR-T cells) and donor lymphocyte infusion (DLI) are important protocols in lymphocyte engineering. CAR-T cells have emerged as a new modality for cancer immunotherapy due to their potential efficacy against hematological malignancies. These genetically mo...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893262/ https://www.ncbi.nlm.nih.gov/pubmed/29662667 http://dx.doi.org/10.18632/oncotarget.24637 |
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author | Tat, Tiberiu Li, Huming Constantinescu, Catalin-Sorin Onaciu, Anca Chira, Sergiu Osan, Ciprian Pasca, Sergiu Petrushev, Bobe Moisoiu, Vlad Micu, Wilhelm-Thomas Berce, Cristian Tranca, Sebastian Dima, Delia Berindan-Neagoe, Ioana Shen, Jianliang Tomuleasa, Ciprian Qian, Liren |
author_facet | Tat, Tiberiu Li, Huming Constantinescu, Catalin-Sorin Onaciu, Anca Chira, Sergiu Osan, Ciprian Pasca, Sergiu Petrushev, Bobe Moisoiu, Vlad Micu, Wilhelm-Thomas Berce, Cristian Tranca, Sebastian Dima, Delia Berindan-Neagoe, Ioana Shen, Jianliang Tomuleasa, Ciprian Qian, Liren |
author_sort | Tat, Tiberiu |
collection | PubMed |
description | Chimeric antigen receptor-modified T cells (CAR-T cells) and donor lymphocyte infusion (DLI) are important protocols in lymphocyte engineering. CAR-T cells have emerged as a new modality for cancer immunotherapy due to their potential efficacy against hematological malignancies. These genetically modified receptors contain an antigen-binding moiety, a hinge region, a transmembrane domain, and an intracellular costimulatory domain resulting in lymphocyte T cell activation subsequent to antigen binding. In present-day medicine, four generations of CAR-T cells are described depending on the intracellular signaling domain number of T cell receptors. DLI represents a form of adoptive therapy used after hematopoietic stem cell transplant for its anti-tumor and anti-infectious properties. This article covers the current status of CAR-T cells and DLI research in the intensive care unit (ICU) patient, including the efficacy, toxicity, side effects and treatment. |
format | Online Article Text |
id | pubmed-5893262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58932622018-04-16 Genetically enhanced T lymphocytes and the intensive care unit Tat, Tiberiu Li, Huming Constantinescu, Catalin-Sorin Onaciu, Anca Chira, Sergiu Osan, Ciprian Pasca, Sergiu Petrushev, Bobe Moisoiu, Vlad Micu, Wilhelm-Thomas Berce, Cristian Tranca, Sebastian Dima, Delia Berindan-Neagoe, Ioana Shen, Jianliang Tomuleasa, Ciprian Qian, Liren Oncotarget Review Chimeric antigen receptor-modified T cells (CAR-T cells) and donor lymphocyte infusion (DLI) are important protocols in lymphocyte engineering. CAR-T cells have emerged as a new modality for cancer immunotherapy due to their potential efficacy against hematological malignancies. These genetically modified receptors contain an antigen-binding moiety, a hinge region, a transmembrane domain, and an intracellular costimulatory domain resulting in lymphocyte T cell activation subsequent to antigen binding. In present-day medicine, four generations of CAR-T cells are described depending on the intracellular signaling domain number of T cell receptors. DLI represents a form of adoptive therapy used after hematopoietic stem cell transplant for its anti-tumor and anti-infectious properties. This article covers the current status of CAR-T cells and DLI research in the intensive care unit (ICU) patient, including the efficacy, toxicity, side effects and treatment. Impact Journals LLC 2018-03-27 /pmc/articles/PMC5893262/ /pubmed/29662667 http://dx.doi.org/10.18632/oncotarget.24637 Text en Copyright: © 2018 Tat et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Tat, Tiberiu Li, Huming Constantinescu, Catalin-Sorin Onaciu, Anca Chira, Sergiu Osan, Ciprian Pasca, Sergiu Petrushev, Bobe Moisoiu, Vlad Micu, Wilhelm-Thomas Berce, Cristian Tranca, Sebastian Dima, Delia Berindan-Neagoe, Ioana Shen, Jianliang Tomuleasa, Ciprian Qian, Liren Genetically enhanced T lymphocytes and the intensive care unit |
title | Genetically enhanced T lymphocytes and the intensive care unit |
title_full | Genetically enhanced T lymphocytes and the intensive care unit |
title_fullStr | Genetically enhanced T lymphocytes and the intensive care unit |
title_full_unstemmed | Genetically enhanced T lymphocytes and the intensive care unit |
title_short | Genetically enhanced T lymphocytes and the intensive care unit |
title_sort | genetically enhanced t lymphocytes and the intensive care unit |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893262/ https://www.ncbi.nlm.nih.gov/pubmed/29662667 http://dx.doi.org/10.18632/oncotarget.24637 |
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