Functional p75 interleukin-2 receptor expression on the fresh blast cells in childhood acute lymphoblastic leukemia with natural killer cell properties

Am J Hematol. 1991 Apr;36(4):259-64. doi: 10.1002/ajh.2830360407.

Abstract

Neoplastic cells of childhood acute lymphoblastic leukemia (ALL) with natural killer (NK) cell properties were studied for the expression of p75 interleukin-2 receptors (IL-2R) and the receptor functions. Freshly prepared blast cells from a patient with ALL had NK cell properties: (1) the phenotype such as CD56+, CD2+, E-rosette+, CD3-, and CD19-; and (2) the presence of spontaneous cytotoxicity against NK-sensitive K562 target cells. Although p55 Tac antigen was not detectable, there was the expression of p75 IL-2R on the freshly prepared blast cells: 70% of the cells reacted with Mik-beta 1 monoclonal antibody against p75 IL-2R as determined by flow cytometry. Two-color flow cytometry revealed that the blast cells expressed both p75 IL-2R and NKH-1. NK activity of the blast cells was augmented by their treatment with 1,000 U/ml recombinant IL-2 (rIL-2): the cytotoxicity level as percentage lysis increased to 38.7% from 22.0% when the normal lymphocyte value increased to 62.1% from 46.2%. Although the blast cells possessed no apparent level of proliferative capacity, the addition of 1,000 U/ml rIL-2 yielded a 2.7-fold increase in their thymidine uptake. These results demonstrate the expression of functional p75 IL-2R on the patient's blast cells with NK cell properties.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Antibodies, Monoclonal
  • Antigens, CD / metabolism
  • Antigens, CD / physiology
  • Blast Crisis / metabolism
  • Blast Crisis / pathology*
  • Blast Crisis / physiopathology
  • Cell Division / drug effects
  • Histocytochemistry
  • Humans
  • Killer Cells, Natural / metabolism
  • Killer Cells, Natural / pathology*
  • Killer Cells, Natural / physiology
  • Killer Cells, Natural / ultrastructure
  • Lymphocytes / pathology
  • Lymphocytes / physiology
  • Lymphocytes / ultrastructure
  • Male
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / metabolism
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / physiopathology
  • Receptors, Interleukin-2 / metabolism
  • Receptors, Interleukin-2 / physiology*
  • Thymidine / metabolism

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • Receptors, Interleukin-2
  • Thymidine