Diamond-Blackfan anemia: promotion of marrow erythropoiesis in vitro by recombinant interleukin-3

Blood. 1989 Apr;73(5):1168-74.

Abstract

To clarify the defective erythropoiesis in eight patients with Diamond-Blackfan anemia, we studied their bone marrow response in vitro to recombinant human interleukin-3 (IL-3) and recombinant granulocyte-macrophage colony-stimulating factor (GM-CSF). In an erythropoietin-containing assay system, specimens from six of the eight patients yielded low numbers of erythroid colonies compared to control values, and in five of these no erythropoietin dose-response could be elicited. Addition of IL-3, GM-CSF or both to cultures from the six patients had no effect on CFU-E-derived colonies. In contrast, IL-3 but not GM-CSF induced a marked increase in the number (183%) and size of the BFU-E-derived colonies in five of the six cases and partially corrected the impaired dose-response to erythropoietin in four. Bone marrow from the other two patients yielded numbers of CFU-E and BFU-E colonies comparable to controls and manifested similar increments in colonies with increasing concentrations of erythropoietin. When IL-3 was added to these cultures, further increments were observed in the number and size of BFU-E colonies. We conclude that IL-3 enhanced the marrow erythropoiesis in most of the patients and exerted a corrective effect on the aberrant colony formation in the presence of erythropoietin. The data raise the possibility of IL-3 as a therapeutic agent in Diamond-Blackfan anemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Aplastic / blood
  • Anemia, Aplastic / pathology*
  • Bone Marrow / pathology*
  • Child
  • Child, Preschool
  • Colony-Forming Units Assay
  • Colony-Stimulating Factors / pharmacology
  • Erythropoiesis / drug effects*
  • Female
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Growth Substances / pharmacology
  • Hematopoietic Stem Cells / pathology
  • Hematopoietic Stem Cells / physiology
  • Humans
  • Infant
  • Interleukin-3 / pharmacology*
  • Male
  • Recombinant Proteins / pharmacology*

Substances

  • Colony-Stimulating Factors
  • Growth Substances
  • Interleukin-3
  • Recombinant Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor