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Inhibition of activation induced CD154 on CD4 + CD25 − cells: a valid surrogate for human Treg suppressor function
- Source :
- Immunology & Cell Biology. 90:812-821
- Publication Year :
- 2012
- Publisher :
- Wiley, 2012.
-
Abstract
- Natural Regulatory T cells (Tregs) are defined by stable expression of the cell surface proteins CD4 and CD25, low surface expression of CD127 and expression of the transcription factor FOXP3. The contribution of Treg to the prevention of autoimmunity and the maintenance of immune homoestasis is the subject of ongoing interest, as alterations in Treg numbers and function are implicated in a wide range of diseases. The in vitro benchmark for determining Treg function is suppression of proliferation of unmatched effector T cells in a mixed lymphocyte reaction (MLR) over a 3-6-day time period. As an alternative to this assay, we show that a 7-h CD154 expression assay is rapid, simple and provides a reliable readout of suppressor function. Using multiple Treg-like cell types including natural (n)Treg, inducible (i)Treg and Treg cell lines, we show that suppression of CD154 expression is a surrogate for suppression of proliferation. We propose this as a suitable alternative to the MLR assay, as it is rapid and may be more amenable to high-throughput screening, analysing large cohorts of clinical samples or assaying transiently suppressive populations.
- Subjects :
- Adult
Male
CD40 Ligand
Immunology
chemical and pharmacologic phenomena
Biology
Lymphocyte Activation
T-Lymphocytes, Regulatory
Cell Line
Immune system
Humans
Immunology and Allergy
IL-2 receptor
CD154
Interleukin-7 receptor
Cell Proliferation
Immunoassay
Staining and Labeling
Cell growth
Effector
Cell Membrane
Interleukin-2 Receptor alpha Subunit
FOXP3
Forkhead Transcription Factors
hemic and immune systems
Cell Biology
Fetal Blood
Mixed lymphocyte reaction
Phenotype
Cancer research
Lymphocyte Culture Test, Mixed
Subjects
Details
- ISSN :
- 14401711 and 08189641
- Volume :
- 90
- Database :
- OpenAIRE
- Journal :
- Immunology & Cell Biology
- Accession number :
- edsair.doi.dedup.....5eb89bb199b22102ccf7da67b0bde867
- Full Text :
- https://doi.org/10.1038/icb.2012.18