Erythropoietin administration is associated with improved T-cell properties in patients with myelodysplastic syndromes

Naamit Deshet-Unger, Howard S. Oster, Sara Prutchi-Sagiv, Nir Maaravi, Nataliya Golishevski, Drorit Neumann, Moshe Mittelman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The immune system is impaired in myelodysplastic syndromes (MDS) and plays a role in the pathogenesis of the disease. Here we show effects of recombinant human erythropoietin (rHuEPO) on T cell (CD4+, CD8+ and CD4+CD25+) number and function in MDS patients. Healthy (20 subjects), MDS patients without rHuEPO treatment ('MDS', 13), and MDS patients treated with rHuEPO ('MDS + EPO', 17) were examined. CD4+ and CD8+ T cell numbers were reduced and increased respectively in MDS compared to healthy subjects. EPO treatment normalized these levels. CD4+CD25+ cell numbers, lower in MDS, were normalized in MDS + EPO. In vitro activation of CD4+ and CD8+ cells with phytohemagglutinin as measured by CD69 expression, demonstrated a 7.2 fold increase in CD4+ activation vs 13.6 fold for MDS and MDS + EPO respectively (p = 0.004); and 10.2 fold (MDS) vs 18.6 fold (MDS + EPO, p < 0.003) for CD8+ T cells. Expression of the co-stimulatory marker CD28, decreased in CD4+ and CD8+ T cells in MDS, was normalized in MDS + EPO CD4+ T cells. Subgroup analysis of milder disease (WHO RA and RARS) and more advanced disease revealed no difference in CD4+ and CD8+ T cell numbers. However, the activation of these cells in the RA/RARS subgroup was impaired in EPO-untreated and enhanced in EPO-treated MDS patients. Our data suggest that EPO treatment improves immune abnormalities in MDS and may depend on disease severity.

Original languageEnglish
Pages (from-to)20-27
Number of pages8
JournalLeukemia Research
Volume52
DOIs
StatePublished - 1 Jan 2017

Funding

FundersFunder number
Israel Cancer Association

    Keywords

    • Erythropoietin
    • Immune modulation
    • Lymphocytes
    • Myelodysplastic syndrome
    • T cells

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