Quantitative analysis of Howell-Jolly bodies in children with sickle cell disease

Exp Hematol. 2007 Feb;35(2):179-83. doi: 10.1016/j.exphem.2006.09.013.

Abstract

Objectives: Although functional asplenia in sickle cell disease (SCD) begins early in life and has important clinical consequences, quantitative measurement of splenic function is not readily available. A novel high-throughput flow cytometric method for quantitating Howell-Jolly bodies (HJB) has been developed which isolates HJB-containing CD71(+) and CD71(-) erythrocytes. Analysis of these cell populations allows quantitative measurement of splenic filtrative function and possible chromosomal damage.

Methods: Blood specimens from 147 children with SCD were analyzed using a high-throughput flow cytometric method. Enumeration of the following populations was accomplished: 1) CD71(+) reticulocytes among total erythrocytes, identifying the youngest erythroid cell population; 2) HJB-containing CD71(+) reticulocytes, which isolate young erythrocytes containing micronuclei as an index of cytogenetic damage; and 3) HJB-containing CD71(-) erythrocytes, identifying older erythrocytes containing micronuclei, indirectly measuring splenic function.

Results: Children with HbSC (n = 24) had slightly elevated HJB frequencies, while children with HbSS (n = 125) had highly elevated frequencies within CD71(+) cells (0.44% +/- 0.40%, normal 0.12% +/- 0.06%, p < 0.001) and CD71(-) cells (2493 +/- 2303 per million RBC, normal 20 +/- 11, p < 0.001). Using a multiple regression model, the frequency of HbSS CD71(+) reticulocytes containing HJB was significantly influenced by hydroxyurea use (p < 0.0001), age (p = 0.0288), and splenectomy (p = 0.0498). Similarly, mature CD71(-) erythrocytes containing HJB were positively correlated with hydroxyurea (p = 0.0001), age (p < 0.0001), and splenectomy (p = 0.0104).

Conclusions: HJB quantitation by flow cytometry is a novel assay for measuring splenic function and may be valuable for investigating the efficacy and safety of therapeutic options for children with SCD.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Sickle Cell / blood*
  • Anemia, Sickle Cell / genetics
  • Anemia, Sickle Cell / metabolism
  • Antigens, CD / metabolism
  • Child
  • Child, Preschool
  • Cohort Studies
  • Erythrocyte Inclusions / metabolism
  • Erythrocyte Inclusions / pathology*
  • Erythrocytes / metabolism
  • Erythrocytes / pathology
  • Female
  • Flow Cytometry / methods*
  • Genotype
  • Hemoglobin, Sickle / analysis
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Micronucleus Tests
  • Receptors, Transferrin / metabolism
  • Reproducibility of Results
  • Reticulocytes / metabolism
  • Reticulocytes / pathology
  • Splenectomy

Substances

  • Antigens, CD
  • CD71 antigen
  • Hemoglobin, Sickle
  • Receptors, Transferrin