University of Adelaide Library

Adelaide Research and Scholarship : Schools and Disciplines : School of Paediatrics & Reproductive Health : Paediatrics : Paediatrics publications

Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/74232

Type: Journal article
Title: Inhibition of activation induced CD154 on CD4⁺ CD25⁻ cells: a valid surrogate for human Treg suppressor function
Other Titles: Inhibition of activation induced CD154 on CD4+ CD25- cells: a valid surrogate for human Treg suppressor function
Author: Hill, D.
Eastaff-Leung, N.
Bresatz-Atkins, S.
Warner, N.
Ruitenberg, J.
Krumbiegel, D.
Pederson, S.
McInnes, N.
Brown, C.
Sadlon, T.
Barry, S.
Citation: Immunology and Cell Biology, 2012; 90(8):812-821
Publisher: Blackwell Publishing Asia
Issue Date: 2012
ISSN: 0818-9641
1440-1711
Statement of
Responsibility: 
Danika Hill, Nicola Eastaff-Leung, Suzanne Bresatz-Atkins, Noel Warner, Joyce Ruitenberg, Dorren Krumbiegel, Steve Pederson, Natasha McInnes, Cheryl Y. Brown, Timothy Sadlon and Simon C. Barry
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. Keywords: regulatory T cells; functional assays; iTreg; nTreg
Keywords: Regulatory T cells; functional assays; iTreg; nTreg
Rights: © 2012 Australasian Society for Immunology
RMID: 0020121555
DOI: 10.1038/icb.2012.18
Appears in Collections:Paediatrics publications
View citing articles in: Web of Science
Google Scholar
Scopus

Files in This Item:

File Description SizeFormat
hdl_74232.pdfAccepted version2.18 MBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

© 2008 The University of Adelaide
library@adelaide.edu.au
CRICOS Provider Number 00123M
Service Charter | Copyright | Privacy | Disclaimer