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Comparing thermal stress reduction strategies that influence MDSC accumulation in tumor bearing mice
- Source :
- Cell Immunol
- Publication Year :
- 2020
-
Abstract
- Myeloid derived suppressor cells (MDSCs) are a diverse collection of immune cells that suppress anti-tumor immune responses. Decreasing MDSCs accumulation in the tumor microenvironment could improve the anti-tumor immune response and improve immunotherapy. Here, we examine the impact of physiologically relevant thermal treatments on the accumulation of MDSCs in tumors in mice. We found that different temperature-based protocols, including 1) weekly whole-body hyperthermia, 2) housing mice at their thermoneutral temperature (TT, ~30 °C), and 3) housing mice at a subthermoneutral temperature (ST,~22 °C) while providing a localized heat source, each resulted in a reduction in MDSC accumulation and improved tumor growth control compared to control mice housed at ST, which is the standard, mandated housing temperature for laboratory mice. Additionally, we found that low dose β-adrenergic receptor blocker (propranolol) therapy reduced MDSC accumulation and improved tumor growth control to a similar degree as the models that relieved cold stress. These results show that thermal treatments can decrease MDSC accumulation and tumor growth comparable to propranolol therapy.
- Subjects :
- 0301 basic medicine
Hyperthermia
Male
Hot Temperature
medicine.medical_treatment
Immunology
Adrenergic beta-Antagonists
Propranolol
Biology
Article
Heating
03 medical and health sciences
Mice
0302 clinical medicine
Immune system
Cell Line, Tumor
Neoplasms
medicine
Tumor Microenvironment
Animals
Tumor growth
Receptor
Tumor microenvironment
Mice, Inbred BALB C
Myeloid-Derived Suppressor Cells
Immunotherapy
Hyperthermia, Induced
medicine.disease
030104 developmental biology
Cancer research
Myeloid-derived Suppressor Cell
Female
Heat-Shock Response
030215 immunology
medicine.drug
Subjects
Details
- ISSN :
- 10902163
- Volume :
- 361
- Database :
- OpenAIRE
- Journal :
- Cellular immunology
- Accession number :
- edsair.doi.dedup.....010398a0a57d4a7928de25ac3792a77d