Diamond-Blackfan syndrome: a possible role of cellular factors for erythropoietic suppression

Scand J Haematol. 1985 Aug;35(2):158-65. doi: 10.1111/j.1600-0609.1985.tb01565.x.

Abstract

CFU-E growth from fractionated bone marrow cells of 5 children with Diamond-Blackfan syndrome was studied. In all patients, CFU-E growth was reduced in mononuclear cell-rich fraction. In 2 of the 5 patients, CFU-E growth was returned to normal by the depletion of E-rosette forming cells or monocytes from mononuclear cell-rich fraction. In the patient whose CFU-E growth returned to normal by the depletion of E-rosette forming cells, co-cultivation between bone marrow buffy coat cells and autologous bone marrow E-rosette forming cells resulted in a significant decrease of CFU-E growth, and there was a significant increase in CFU-E growth by treatment with monoclonal antiserum to OKT4. We concluded that immunologic causes such as cellular factors may play a role, at least in part, in the pathogenesis of Diamond-Blackfan syndrome.

MeSH terms

  • Anemia, Aplastic / blood
  • Anemia, Aplastic / pathology*
  • Antibodies, Monoclonal / immunology
  • Bone Marrow Cells*
  • Cell Communication
  • Cell Separation
  • Cells, Cultured
  • Child, Preschool
  • Colony-Forming Units Assay
  • Densitometry
  • Erythropoiesis*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Lymphocytes / immunology
  • Male
  • Monocytes / immunology
  • Red-Cell Aplasia, Pure / blood
  • Red-Cell Aplasia, Pure / pathology*
  • Rosette Formation

Substances

  • Antibodies, Monoclonal