Journal article
TCR-mediated functions are enhanced in activated peripheral blood T cells isolated from leucocyte reduction systems
Journal of immunological methods, Vol.416, pp.137-145
01/2015
DOI: 10.1016/j.jim.2014.11.009
PMCID: PMC4324009
PMID: 25462023
Abstract
Buffy coats are the most common method for the acquisition of activated primary human T cells for research or clinical applications, but recently leukocyte reduction system (LRS) cones have emerged as a viable source for these cells. In this study, we determined if activated human T cells derived from buffy coats or LRS cones had different functionality. No changes in the expression of surface receptors were observed except for a significant increase in CD44 expression on T cells isolated from LRS cones. LRS cone-derived T cells trended towards higher receptor-mediated cytokine production and had significantly increased donor-to-donor variability in IFN-γ production. TCR-induced ERK1/ERK2 and AKT phosphorylation was also increased in T cells isolated from LRS cones. In conclusion, LRS cones are an excellent source of T cells for clinical and research applications, but these cells have subtle functional differences from T cells isolated using standard buffy coats.
Details
- Title: Subtitle
- TCR-mediated functions are enhanced in activated peripheral blood T cells isolated from leucocyte reduction systems
- Creators
- Mikaela M Tremblay - Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, United StatesJon C D Houtman - Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, United States. Electronic address: jon-houtman@uiowa.edu
- Resource Type
- Journal article
- Publication Details
- Journal of immunological methods, Vol.416, pp.137-145
- DOI
- 10.1016/j.jim.2014.11.009
- PMID
- 25462023
- PMCID
- PMC4324009
- NLM abbreviation
- J Immunol Methods
- ISSN
- 0022-1759
- eISSN
- 1872-7905
- Publisher
- Elsevier BV
- Grant note
- R01 CA136729 / NCI NIH HHS
- Language
- English
- Date published
- 01/2015
- Academic Unit
- Microbiology and Immunology; Internal Medicine
- Record Identifier
- 9984094526502771
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