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Selenium status and phytohemagglutinin-stimulated T lymphocytes from beef calves
1Departments of Animal Science, North Carolina A&T State University, 27411, Greensboro, North Carolina.
Biological Trace Element Research
|November 22, 2013
Summary
Selenium supplementation did not affect T lymphocyte blastogenesis in calves. However, lymphocyte response to phytohemagglutinin (PHA) stimulation varied with age, being highest in younger calves.
Area of Science:
- Veterinary Immunology
- Animal Nutrition
- Cellular Immunology
Background:
- Selenium (Se) is a vital trace element influencing immune function.
- Assessing T lymphocyte blastogenesis is crucial for evaluating cellular immunity in cattle.
- Geographical areas with low soil selenium can lead to marginal deficiencies in livestock.
Purpose of the Study:
- To investigate the impact of selenium (Se) supplementation on in vitro phytohemagglutinin (PHA)-stimulated T lymphocyte blastogenesis in calves.
- To determine the effects of calf age on T lymphocyte responsiveness.
Main Methods:
- Crossbred calves (n=8) were divided into control and Se-treated groups.
- Selenium was administered via subcutaneous injections.
- Peripheral blood lymphocytes were cultured with PHA and [(3)H]-thymidine to measure thymidine incorporation.
- Stimulation index (SI) was calculated to assess lymphocyte blastogenesis.
Main Results:
- Se-treated calves achieved adequate selenium status, confirmed by plasma Se and glutathione peroxidase levels.
- Selenium treatment did not significantly influence T lymphocyte blastogenesis (SI values).
- Lymphocyte stimulation index (SI) was significantly affected by age, with higher responses observed in younger calves (45 days) compared to older calves (124 and 270 days).
Conclusions:
- Selenium supplementation did not alter T lymphocyte responsiveness to PHA stimulation in beef calves.
- Age significantly impacts T lymphocyte blastogenesis, with younger calves exhibiting greater responsiveness.
- Beef calves in selenium-deficient regions may maintain normal T lymphocyte function despite marginal selenium status.

