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Modulation of anti-tumor immunity by the brain’s reward system

Regulating immunity is a leading target for cancer therapy. Here, we show that the anti-tumor immune response can be modulated by the brain’s reward system, a key circuitry in emotional processes. Activation of the reward system in tumor-bearing mice (Lewis lung carcinoma (LLC) and B16 melanoma) usi...

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Autores principales: Ben-Shaanan, Tamar L, Schiller, Maya, Azulay-Debby, Hilla, Korin, Ben, Boshnak, Nadia, Koren, Tamar, Krot, Maria, Shakya, Jivan, Rahat, Michal A., Hakim, Fahed, Rolls, Asya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045610/
https://www.ncbi.nlm.nih.gov/pubmed/30006573
http://dx.doi.org/10.1038/s41467-018-05283-5
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author Ben-Shaanan, Tamar L
Schiller, Maya
Azulay-Debby, Hilla
Korin, Ben
Boshnak, Nadia
Koren, Tamar
Krot, Maria
Shakya, Jivan
Rahat, Michal A.
Hakim, Fahed
Rolls, Asya
author_facet Ben-Shaanan, Tamar L
Schiller, Maya
Azulay-Debby, Hilla
Korin, Ben
Boshnak, Nadia
Koren, Tamar
Krot, Maria
Shakya, Jivan
Rahat, Michal A.
Hakim, Fahed
Rolls, Asya
author_sort Ben-Shaanan, Tamar L
collection PubMed
description Regulating immunity is a leading target for cancer therapy. Here, we show that the anti-tumor immune response can be modulated by the brain’s reward system, a key circuitry in emotional processes. Activation of the reward system in tumor-bearing mice (Lewis lung carcinoma (LLC) and B16 melanoma) using chemogenetics (DREADDs), resulted in reduced tumor weight. This effect was mediated via the sympathetic nervous system (SNS), manifested by an attenuated noradrenergic input to a major immunological site, the bone marrow. Myeloid derived suppressor cells (MDSCs), which develop in the bone marrow, became less immunosuppressive following reward system activation. By depleting or adoptively transferring the MDSCs, we demonstrated that these cells are both necessary and sufficient to mediate reward system effects on tumor growth. Given the central role of the reward system in positive emotions, these findings introduce a physiological mechanism whereby the patient’s psychological state can impact anti-tumor immunity and cancer progression.
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spelling pubmed-60456102018-07-16 Modulation of anti-tumor immunity by the brain’s reward system Ben-Shaanan, Tamar L Schiller, Maya Azulay-Debby, Hilla Korin, Ben Boshnak, Nadia Koren, Tamar Krot, Maria Shakya, Jivan Rahat, Michal A. Hakim, Fahed Rolls, Asya Nat Commun Article Regulating immunity is a leading target for cancer therapy. Here, we show that the anti-tumor immune response can be modulated by the brain’s reward system, a key circuitry in emotional processes. Activation of the reward system in tumor-bearing mice (Lewis lung carcinoma (LLC) and B16 melanoma) using chemogenetics (DREADDs), resulted in reduced tumor weight. This effect was mediated via the sympathetic nervous system (SNS), manifested by an attenuated noradrenergic input to a major immunological site, the bone marrow. Myeloid derived suppressor cells (MDSCs), which develop in the bone marrow, became less immunosuppressive following reward system activation. By depleting or adoptively transferring the MDSCs, we demonstrated that these cells are both necessary and sufficient to mediate reward system effects on tumor growth. Given the central role of the reward system in positive emotions, these findings introduce a physiological mechanism whereby the patient’s psychological state can impact anti-tumor immunity and cancer progression. Nature Publishing Group UK 2018-07-13 /pmc/articles/PMC6045610/ /pubmed/30006573 http://dx.doi.org/10.1038/s41467-018-05283-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ben-Shaanan, Tamar L
Schiller, Maya
Azulay-Debby, Hilla
Korin, Ben
Boshnak, Nadia
Koren, Tamar
Krot, Maria
Shakya, Jivan
Rahat, Michal A.
Hakim, Fahed
Rolls, Asya
Modulation of anti-tumor immunity by the brain’s reward system
title Modulation of anti-tumor immunity by the brain’s reward system
title_full Modulation of anti-tumor immunity by the brain’s reward system
title_fullStr Modulation of anti-tumor immunity by the brain’s reward system
title_full_unstemmed Modulation of anti-tumor immunity by the brain’s reward system
title_short Modulation of anti-tumor immunity by the brain’s reward system
title_sort modulation of anti-tumor immunity by the brain’s reward system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045610/
https://www.ncbi.nlm.nih.gov/pubmed/30006573
http://dx.doi.org/10.1038/s41467-018-05283-5
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