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Harnessing NK Cells for Cancer Treatment
In the last years, natural killer (NK) cell-based immunotherapy has emerged as a promising therapeutic approach for solid tumors and hematological malignancies. NK cells are innate lymphocytes with an array of functional competences, including anti-cancer, anti-viral, and anti-graft-vs.-host disease...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908847/ https://www.ncbi.nlm.nih.gov/pubmed/31867006 http://dx.doi.org/10.3389/fimmu.2019.02836 |
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author | Minetto, Paola Guolo, Fabio Pesce, Silvia Greppi, Marco Obino, Valentina Ferretti, Elisa Sivori, Simona Genova, Carlo Lemoli, Roberto Massimo Marcenaro, Emanuela |
author_facet | Minetto, Paola Guolo, Fabio Pesce, Silvia Greppi, Marco Obino, Valentina Ferretti, Elisa Sivori, Simona Genova, Carlo Lemoli, Roberto Massimo Marcenaro, Emanuela |
author_sort | Minetto, Paola |
collection | PubMed |
description | In the last years, natural killer (NK) cell-based immunotherapy has emerged as a promising therapeutic approach for solid tumors and hematological malignancies. NK cells are innate lymphocytes with an array of functional competences, including anti-cancer, anti-viral, and anti-graft-vs.-host disease potential. The intriguing idea of harnessing such potent innate immune system effectors for cancer treatment led to the development of clinical trials based on the adoptive therapy of NK cells or on the use of monoclonal antibodies targeting the main NK cell immune checkpoints. Indeed, checkpoint immunotherapy that targets inhibitory receptors of T cells, reversing their functional blocking, marked a breakthrough in anticancer therapy, opening new approaches for cancer immunotherapy and resulted in extensive research on immune checkpoints. However, the clinical efficacy of T cell-based immunotherapy presents a series of limitations, including the inability of T cells to recognize and kill HLA-I(neg) tumor cells. For these reasons, new strategies for cancer immunotherapy are now focusing on NK cells. Blockade with NK cell checkpoint inhibitors that reverse their functional block may overcome the limitations of T cell-based immunotherapy, mainly against HLA-I(neg) tumor targets. Here, we discuss recent anti-tumor approaches based on mAb-mediated blocking of immune checkpoints (either restricted to NK cells or shared with T cells), used either as a single agent or in combination with other compounds, that have demonstrated promising clinical responses in both solid tumors and hematological malignancies. |
format | Online Article Text |
id | pubmed-6908847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69088472019-12-20 Harnessing NK Cells for Cancer Treatment Minetto, Paola Guolo, Fabio Pesce, Silvia Greppi, Marco Obino, Valentina Ferretti, Elisa Sivori, Simona Genova, Carlo Lemoli, Roberto Massimo Marcenaro, Emanuela Front Immunol Immunology In the last years, natural killer (NK) cell-based immunotherapy has emerged as a promising therapeutic approach for solid tumors and hematological malignancies. NK cells are innate lymphocytes with an array of functional competences, including anti-cancer, anti-viral, and anti-graft-vs.-host disease potential. The intriguing idea of harnessing such potent innate immune system effectors for cancer treatment led to the development of clinical trials based on the adoptive therapy of NK cells or on the use of monoclonal antibodies targeting the main NK cell immune checkpoints. Indeed, checkpoint immunotherapy that targets inhibitory receptors of T cells, reversing their functional blocking, marked a breakthrough in anticancer therapy, opening new approaches for cancer immunotherapy and resulted in extensive research on immune checkpoints. However, the clinical efficacy of T cell-based immunotherapy presents a series of limitations, including the inability of T cells to recognize and kill HLA-I(neg) tumor cells. For these reasons, new strategies for cancer immunotherapy are now focusing on NK cells. Blockade with NK cell checkpoint inhibitors that reverse their functional block may overcome the limitations of T cell-based immunotherapy, mainly against HLA-I(neg) tumor targets. Here, we discuss recent anti-tumor approaches based on mAb-mediated blocking of immune checkpoints (either restricted to NK cells or shared with T cells), used either as a single agent or in combination with other compounds, that have demonstrated promising clinical responses in both solid tumors and hematological malignancies. Frontiers Media S.A. 2019-12-06 /pmc/articles/PMC6908847/ /pubmed/31867006 http://dx.doi.org/10.3389/fimmu.2019.02836 Text en Copyright © 2019 Minetto, Guolo, Pesce, Greppi, Obino, Ferretti, Sivori, Genova, Lemoli and Marcenaro. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Minetto, Paola Guolo, Fabio Pesce, Silvia Greppi, Marco Obino, Valentina Ferretti, Elisa Sivori, Simona Genova, Carlo Lemoli, Roberto Massimo Marcenaro, Emanuela Harnessing NK Cells for Cancer Treatment |
title | Harnessing NK Cells for Cancer Treatment |
title_full | Harnessing NK Cells for Cancer Treatment |
title_fullStr | Harnessing NK Cells for Cancer Treatment |
title_full_unstemmed | Harnessing NK Cells for Cancer Treatment |
title_short | Harnessing NK Cells for Cancer Treatment |
title_sort | harnessing nk cells for cancer treatment |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908847/ https://www.ncbi.nlm.nih.gov/pubmed/31867006 http://dx.doi.org/10.3389/fimmu.2019.02836 |
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