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Output Category: C1: Journal Article (Schol Refereed Journal)
Strategic Research Area:
TISI Citations: 4 PlumX StatisticsPlumX Statistics
Scopus Citations: 3
Journal Impact: 1.99
All Authors: Tan, D, Fernandez, S, Price, P, Moodley, Y Number: 4
UWA Authors: Tan, D., Fernández, S., Price, P., Moodley, Y. Number: 3
Title: The proportion and function of peripheral myeloid-derived suppressor cells do not correlate with systemic inflammation in chronic obstructive pulmonary disease
Journal: Human Immunology   
ISBN/ISSN 0198-8859
Year: 2014
Pages: 5-9
Volume: 75
Issue: 1
Full Reference (Harvard Style): Tan, D., Fernández, S., Price, P., Moodley, Y. 2014, 'The proportion and function of peripheral myeloid-derived suppressor cells do not correlate with systemic inflammation in chronic obstructive pulmonary disease', Human Immunology, 75, 1, pp. 5-9.
Abstract:
Myeloid-derived suppressor cells (MDSC) have been implicated in the regulation of chronic inflammation. Chronic obstructive pulmonary disease (COPD) involves persistent inflammation, but the role of MDSC has not been explored. Here, proportions of MDSC (CD14-HLA-DR-CD33+CD11b+ cells) were quantified in peripheral blood mononuclear cells (PBMC) isolated from patients with 'stable' COPD (n=12), smokers with no evidence of COPD (n=11) and healthy non-smokers (n=11). The proportions of MDSC were similar in all groups. MDSC function was assessed by comparing T-cell and cytokine responses of whole and MDSC-depleted PBMC stimulated with Staphylococcus enterotoxin-B (SEB). Depletion of MDSC did not enhance CD4+ or CD8+ T-cell activation and proliferation, or alter IFNγ and IL-17 production in response to SEB. However production of TGFβ decreased after depletion of MDSC, so MDSC may be a source of this cytokine. In conclusion, COPD was not associated with perturbations in the proportion or function of MDSC in peripheral blood. © 2013 American Society for Histocompatibility and Immunogenetics.