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Peptide:MHC Tetramer-based Enrichment of Epitope-specific T cells
Published on: October 22, 2012
Naive and memory T cell subsets are differentially mobilized during physical stress
G A Gannon1, S Rhind, P N Shek
1Defence & Civil Institute of Environmental Medicine, Toronto, ON, Canada.
International Journal of Sports Medicine
|March 27, 2002
Summary
Combined aerobic exercise and heat stress mobilized CD4+ T cells with a memory phenotype, while CD8hi T cell mobilization was independent of memory phenotype but influenced by adhesion molecules CD11a and CD62L.
Area of Science:
- Immunology
- Exercise Physiology
- Environmental Stress
Background:
- T cell mobilization plays a crucial role in immune surveillance and response.
- Understanding T cell phenotypes during combined physiological stressors like exercise and heat is vital for immune function insights.
Purpose of the Study:
- To investigate the naive and memory phenotypic profiles of CD4+ and CD8hi T cells mobilized during combined aerobic exercise and heat stress.
- To determine the expression of adhesion molecules CD62L and CD11a on these mobilized T cells.
Main Methods:
- Twelve healthy males underwent 40 minutes of cycle ergometry at 65% VO2peak in a 39°C water bath.
- Blood samples were collected pre-exercise, during exercise, and post-exercise.
- Three-color flow cytometry was used to analyze CD4+ and CD8hi T cell expression of CD45RO, CD11a, and CD62L.
Main Results:
- Approximately 80% of mobilized CD4+ T cells exhibited a CD45RO memory phenotype.
- Mobilized CD8hi T cells showed a near-equal recruitment of naive (43%) and memory (57%) cells.
- High expression of CD11a and low expression of CD62L were key factors in CD8hi T cell mobilization.
Conclusions:
- The mobilization of CD4+ T cells during exercise and heat stress is associated with a memory phenotype, not solely explained by CD11a and CD62L expression.
- CD8hi T cell mobilization is independent of memory phenotype but significantly influenced by high CD11a expression and low CD62L expression, indicating altered adhesion and homing receptor function.
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