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Control of NK Cell Activation by Immune Checkpoint Molecules
The development of cancer and chronic infections is facilitated by many subversion mechanisms, among which enhanced expression of immune checkpoints molecules, such as programmed death-1 (PD-1) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), on exhausted T cells. Recently, immune checkpoin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666811/ https://www.ncbi.nlm.nih.gov/pubmed/29023417 http://dx.doi.org/10.3390/ijms18102129 |
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author | Beldi-Ferchiou, Asma Caillat-Zucman, Sophie |
author_facet | Beldi-Ferchiou, Asma Caillat-Zucman, Sophie |
author_sort | Beldi-Ferchiou, Asma |
collection | PubMed |
description | The development of cancer and chronic infections is facilitated by many subversion mechanisms, among which enhanced expression of immune checkpoints molecules, such as programmed death-1 (PD-1) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), on exhausted T cells. Recently, immune checkpoint inhibitors have shown remarkable efficiency in the treatment of a number of cancers. However, expression of immune checkpoints on natural killer (NK) cells and its functional consequences on NK cell effector functions are much less explored. In this review, we focus on the current knowledge on expression of various immune checkpoints in NK cells, how it can alter NK cell-mediated cytotoxicity and cytokine production. Dissecting the role of these inhibitory mechanisms in NK cells is critical for the full understanding of the mode of action of immunotherapies using checkpoint inhibitors in the treatment of cancers and chronic infections. |
format | Online Article Text |
id | pubmed-5666811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56668112017-11-09 Control of NK Cell Activation by Immune Checkpoint Molecules Beldi-Ferchiou, Asma Caillat-Zucman, Sophie Int J Mol Sci Review The development of cancer and chronic infections is facilitated by many subversion mechanisms, among which enhanced expression of immune checkpoints molecules, such as programmed death-1 (PD-1) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), on exhausted T cells. Recently, immune checkpoint inhibitors have shown remarkable efficiency in the treatment of a number of cancers. However, expression of immune checkpoints on natural killer (NK) cells and its functional consequences on NK cell effector functions are much less explored. In this review, we focus on the current knowledge on expression of various immune checkpoints in NK cells, how it can alter NK cell-mediated cytotoxicity and cytokine production. Dissecting the role of these inhibitory mechanisms in NK cells is critical for the full understanding of the mode of action of immunotherapies using checkpoint inhibitors in the treatment of cancers and chronic infections. MDPI 2017-10-12 /pmc/articles/PMC5666811/ /pubmed/29023417 http://dx.doi.org/10.3390/ijms18102129 Text en © 2017 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 Beldi-Ferchiou, Asma Caillat-Zucman, Sophie Control of NK Cell Activation by Immune Checkpoint Molecules |
title | Control of NK Cell Activation by Immune Checkpoint Molecules |
title_full | Control of NK Cell Activation by Immune Checkpoint Molecules |
title_fullStr | Control of NK Cell Activation by Immune Checkpoint Molecules |
title_full_unstemmed | Control of NK Cell Activation by Immune Checkpoint Molecules |
title_short | Control of NK Cell Activation by Immune Checkpoint Molecules |
title_sort | control of nk cell activation by immune checkpoint molecules |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666811/ https://www.ncbi.nlm.nih.gov/pubmed/29023417 http://dx.doi.org/10.3390/ijms18102129 |
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