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Updated: Aug 15, 2026

Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice
Published on: June 22, 2016
Regulation of cellular immune responses by selenium
L Kiremidjian-Schumacher1, M Roy, H I Wishe
1New York University, Dental Center, Department of Oral Medicine and Pathology, N.Y. 10010.
Selenium supplementation enhances immune cell proliferation and tumor cytotoxicity. Selenium deficiency impairs these responses, impacting cell-mediated immunity and macrophage activity.
Area of Science:
- Immunology
- Nutritional Science
- Oncology
Background:
- Selenium (Se) is a vital nutrient influencing immune responses against cancer.
- Cell-mediated immunity, crucial for tumor surveillance, is modulated by nutritional factors.
Purpose of the Study:
- To investigate the impact of selenium on lymphocyte proliferation and cytotoxic activity.
- To elucidate the role of selenium in immune responses against malignant cells.
Main Methods:
- Mice (C57Bl/6J) were supplemented with selenium (2 ppm) or made deficient (0.02 ppm) for 8 weeks.
- In vitro studies used sodium selenite (1 x 10(-7)M) to assess lymphocyte responses to mitogen/antigen.
- Interleukin-2 (Il2) levels and high-affinity Il2 receptor expression kinetics were analyzed.
Main Results:
- Selenium supplementation significantly enhanced lymphocyte proliferation and cytotoxic cell frequency.
- Selenium deficiency reduced these immune responses.
- Selenium modulated the kinetics of high-affinity Il2 receptor expression, affecting clonal expansion.
- Tumor cytotoxicity and macrophage-mediated cytodestruction were positively correlated with selenium levels.
Conclusions:
- Dietary and in vitro selenium modulates lymphocyte proliferation, cytotoxic activity, and macrophage function.
- Selenium's effects on immune cells occur 8-24 hours post-stimulation, likely within cytoplasmic/nuclear compartments.
- Adequate selenium is crucial for effective cell-mediated anti-tumor immunity.
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