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Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy

A significant function of the immune system is the surveillance and elimination of aberrant cells that give rise to cancer. Even when tumors are well established and metastatic, immune-mediated spontaneous regressions have been documented. While there are have been various forms of immunotherapy, on...

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Autores principales: Visioni, Anthony, Skitzki, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040988/
https://www.ncbi.nlm.nih.gov/pubmed/27657129
http://dx.doi.org/10.3390/cancers8090086
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author Visioni, Anthony
Skitzki, Joseph
author_facet Visioni, Anthony
Skitzki, Joseph
author_sort Visioni, Anthony
collection PubMed
description A significant function of the immune system is the surveillance and elimination of aberrant cells that give rise to cancer. Even when tumors are well established and metastatic, immune-mediated spontaneous regressions have been documented. While there are have been various forms of immunotherapy, one of the most widely studied for almost 40 years is adoptive cellular immunotherapy, but its success has yet to be fully realized. Adoptive cell transfer (ACT) is a therapeutic modality that has intrigued physicians and researchers for its many theoretical benefits. Preclinical investigations and human trials have utilized natural killer (NK) cells, dendritic cells (DC), macrophages, T-cells or B-cells for ACT with the most intense research focused on T-cell ACT. T-cells are exquisitely specific to the target of its T-cell receptor (TCR), thus potentially reducing the amount of collateral damage and off-target effects from treatment. T-cells also possess a memory subset that may reduce the risk of recurrence of a cancer after the successful treatment of the primary disease. There are several options for the source of T-cells used in the generation of cells for ACT. Perhaps the most widely known source is T-cells generated from tumor-infiltrating lymphocytes (TILs). However, studies have also employed peripheral blood mononuclear cells (PBMCs), lymph nodes, and even induced pluripotent stem cells (IPSCs) as a source of T-cells. Several important technical considerations exist regarding benefits and limitations of each source of T-cells. Unique aspects of T-cells factor into their ability to be efficacious in ACT including the total number of cells available for ACT, the anti-tumor efficacy on a per cell basis, the repertoire of TCRs specific to tumor cells, and their ability to traffic to various organs that harbor tumor. Current research is attempting to unlock the full potential of these cells to effectively and safely treat cancer.
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spelling pubmed-50409882016-10-05 Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy Visioni, Anthony Skitzki, Joseph Cancers (Basel) Review A significant function of the immune system is the surveillance and elimination of aberrant cells that give rise to cancer. Even when tumors are well established and metastatic, immune-mediated spontaneous regressions have been documented. While there are have been various forms of immunotherapy, one of the most widely studied for almost 40 years is adoptive cellular immunotherapy, but its success has yet to be fully realized. Adoptive cell transfer (ACT) is a therapeutic modality that has intrigued physicians and researchers for its many theoretical benefits. Preclinical investigations and human trials have utilized natural killer (NK) cells, dendritic cells (DC), macrophages, T-cells or B-cells for ACT with the most intense research focused on T-cell ACT. T-cells are exquisitely specific to the target of its T-cell receptor (TCR), thus potentially reducing the amount of collateral damage and off-target effects from treatment. T-cells also possess a memory subset that may reduce the risk of recurrence of a cancer after the successful treatment of the primary disease. There are several options for the source of T-cells used in the generation of cells for ACT. Perhaps the most widely known source is T-cells generated from tumor-infiltrating lymphocytes (TILs). However, studies have also employed peripheral blood mononuclear cells (PBMCs), lymph nodes, and even induced pluripotent stem cells (IPSCs) as a source of T-cells. Several important technical considerations exist regarding benefits and limitations of each source of T-cells. Unique aspects of T-cells factor into their ability to be efficacious in ACT including the total number of cells available for ACT, the anti-tumor efficacy on a per cell basis, the repertoire of TCRs specific to tumor cells, and their ability to traffic to various organs that harbor tumor. Current research is attempting to unlock the full potential of these cells to effectively and safely treat cancer. MDPI 2016-09-20 /pmc/articles/PMC5040988/ /pubmed/27657129 http://dx.doi.org/10.3390/cancers8090086 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Visioni, Anthony
Skitzki, Joseph
Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy
title Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy
title_full Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy
title_fullStr Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy
title_full_unstemmed Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy
title_short Technical Considerations for the Generation of Adoptively Transferred T Cells in Cancer Immunotherapy
title_sort technical considerations for the generation of adoptively transferred t cells in cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040988/
https://www.ncbi.nlm.nih.gov/pubmed/27657129
http://dx.doi.org/10.3390/cancers8090086
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