Author
Listed:
- Tamar L Ben-Shaanan
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Maya Schiller
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Hilla Azulay-Debby
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Ben Korin
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Nadia Boshnak
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Tamar Koren
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Maria Krot
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
- Jivan Shakya
(Technion - Israel Institute of Technology
Carmel Medical Center)
- Michal A. Rahat
(Technion - Israel Institute of Technology
Carmel Medical Center)
- Fahed Hakim
(Technion - Israel Institute of Technology
Rambam Health Care Campus
Cancer Research Center, EMMS Hospital)
- Asya Rolls
(Technion - Israel Institute of Technology
Technion - Israel Institute of Technology
Technion - Israel Institute of Technology)
Abstract
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.
Suggested Citation
Tamar L Ben-Shaanan & Maya Schiller & Hilla Azulay-Debby & Ben Korin & Nadia Boshnak & Tamar Koren & Maria Krot & Jivan Shakya & Michal A. Rahat & Fahed Hakim & Asya Rolls, 2018.
"Modulation of anti-tumor immunity by the brain’s reward system,"
Nature Communications, Nature, vol. 9(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05283-5
DOI: 10.1038/s41467-018-05283-5
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