Cited by 125Iron Metabolism and DisordersErythropoietin and Anemia TreatmentHemoglobinopathies and Related Disorders

Immunoassay for human serum erythroferrone

Open access
Ganz, Tomas, Jung, Grace, Naeim, Arash, Ginzburg, Yelena, Pakbaz, Zahra, Walter, Patrick B., Kautz, Léon, Nemeth, Elizabeta·2017·Blood

Abstract

Erythroferrone (ERFE) is a glycoprotein hormone secreted by erythroblasts in response to stimulation by erythropoietin (EPO). We previously demonstrated that ERFE messenger RNA expression and serum protein concentration increase in mice subjected to hemorrhage or EPO therapy, that ERFE acts on hepatocytes to suppress hepcidin, and that the resulting decrease in hepcidin augments iron delivery for intensified erythropoiesis. We also showed that ERFE contributes to pathological hepcidin suppression and iron overload in mice with nontransfused β-thalassemia. We now report the development and technical validation of a rabbit monoclonal antibody-based sandwich immunoassay for human ERFE. We use this assay to show that blood loss or EPO administration increases serum ERFE concentrations in humans, and that patients with both nontransfused and transfused β-thalassemia have very high serum ERFE levels, which decrease after blood transfusion. The assay should be useful for human studies of normal and disordered erythropoiesis and its effect on iron homeostasis.

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Crossref · 10.1182/blood-2017-04-777987

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  • In non-transfusion-dependent β-thalassemia patients, serum ERFE levels are high, to ensure iron acquisition for the expanded erythropoiesis.

    “In non-transfusion-dependent β-thalassemia patients, serum ERFE levels are high,105 to ensure iron acquisition for the expanded erythropoiesis.106”

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Authors
Ganz, T., Jung, G., Naeim, A., Ginzburg, Y., Pakbaz, Z., Walter, P. B., Kautz, L., & Nemeth, E.
Affiliations
  • University of California, Los Angeles (US)
  • Department of Medicine and
  • Icahn School of Medicine at Mount Sinai (US)
  • University of California, Riverside (US)
  • University of California, San Francisco (US)
  • Université Toulouse III - Paul Sabatier (FR)
Venue
Blood
Published
2017-09-07
Volume
130
Issue
10
Pages
1243-1246
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2738794292
Cited by
125
References
2
Citations by year
2026: 4 · 2025: 6 · 2024: 7 · 2023: 13 · 2022: 10 · 2021: 27 · 2020: 19 · 2019: 22 · 2018: 16 · 2017: 1
FWCI
12.22
Type
journal article
Language
en
Open access
Locations
  • Blood (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
  • National Institutes of Health (UL1TR001881)
  • National Heart, Lung, and Blood Institute (U54HL119893)
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01DK065029, R01DK107309, P30DK041301, R01DK095112, R01DK107670)
  • National Center for Advancing Translational Sciences
Topics
  • Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
  • Health Sciences › Medicine › Hematology › Erythropoietin and Anemia Treatment
  • Health Sciences › Medicine › Genetics › Hemoglobinopathies and Related Disorders
Keywords
erythroferrone, sandwich immunoassay, monoclonal antibodies, serum protein measurement, erythropoietin, hepcidin, iron homeostasis, erythropoiesis, beta-thalassemia, blood transfusion, hemorrhage, iron overload
MeSH terms
Adult, Aged, Blood Donors, Erythropoiesis, Humans, Immunoassay, Male, Middle Aged, beta-Thalassemia, Peptide Hormones, Young Adult, Hepcidins

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