Granulocyte functions in children with cancer are differentially sensitive to the toxic effect of chemotherapy

Pediatr Res. 1996 May;39(5):835-42. doi: 10.1203/00006450-199605000-00016.

Abstract

To analyze the toxicity associated to chemotherapy upon granulocytes, different functional assays were performed, within days of drug exposure and at time of bone marrow recovery, on polymorphonuclear neutrophils (PMN) from children with cancer. There were no significant postchemotherapy changes in the expression of the different receptors studied nor in the phagocytosis of Staphylococcus aureus 42D. By contrast, a significant decrease was observed in H2O2 production in PMN recently exposed to chemotherapy with both cytofluorometric and chemiluminescence assays. There was also a decrease in the production of O2- and in chemotaxis; finally, the intracellular killing of S. aureus 42D and Escherichia coli was reduced. In patients having recovered from drug-induced bone marrow aplasia, PMN functions were found to be normal except for bactericidal activity which was still defective. The observations indicate that, in patients exposed to chemotherapy, some PMN functions are transiently altered, whereas microorganism cell killing is continuously impaired.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Antineoplastic Agents / adverse effects*
  • Blood Bactericidal Activity / drug effects
  • Bone Marrow / drug effects
  • Chemotaxis, Leukocyte / drug effects
  • Child
  • Child, Preschool
  • Escherichia coli / immunology
  • Female
  • Granulocytes / drug effects*
  • Granulocytes / immunology
  • Granulocytes / physiology*
  • Humans
  • Hydrogen Peroxide / metabolism
  • In Vitro Techniques
  • Male
  • Neoplasms / drug therapy*
  • Neoplasms / immunology
  • Neoplasms / physiopathology*
  • Neutrophils / drug effects
  • Neutrophils / immunology
  • Neutrophils / physiology
  • Phagocytosis / drug effects
  • Receptors, Complement / drug effects
  • Receptors, Complement / metabolism
  • Receptors, IgG / drug effects
  • Receptors, IgG / metabolism
  • Respiratory Burst / drug effects
  • Staphylococcus aureus / immunology
  • Superoxides / metabolism

Substances

  • Antineoplastic Agents
  • Receptors, Complement
  • Receptors, IgG
  • Superoxides
  • Hydrogen Peroxide