Modulation of anti-tumor immunity by the brain's reward system.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30006573.
- Also identified by DOI 10.1038/s41467-018-05283-5 and PMC identifier 6045610.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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.
Medical subject headings
- Carcinoma, Lewis Lung
- Clozapine
- Immunologic Factors
- Melanoma, Experimental
- Myeloid-Derived Suppressor Cells
- Reward
- Ventral Tegmental Area