CD177 expression on neutrophils: in search of a clonal assay for myeloid neoplasia by flow cytometry

Am J Clin Pathol. 2013 Nov;140(5):658-69. doi: 10.1309/AJCPDFBEBQZW1OI7.

Abstract

Objectives: To determine whether the fraction of CD177+ neutrophils might be altered in clonal myeloid disorders, similar to the skewed κ/λ ratio for B-cell lymphomas, and could be used to identify myeloid neoplasms.

Methods: Blood and bone marrow samples were evaluated for the fraction of CD177+ neutrophils by flow cytometry.

Results: Skewed high neutrophil CD177(%) was not associated with neoplasia, but skewed low neutrophil CD177(%) was highly correlated with clonal myeloid disorders at values less than 40%. Specificity of low neutrophil CD177(%) for clonal myeloid disorders was 87% with a 40% cutoff and 95% with a 30% cutoff. Findings were most pronounced for myelodysplasia, with 52% (11/21) containing fewer than 40% CD177+ neutrophils. Specificity was also suggested by normalization of neutrophil CD177(%) in four patients who reached morphologic remission after therapy for myelodysplasia or acute leukemia.

Conclusions: Skewed low neutrophil CD177(%) is highly associated with clonal myeloid disorders, particularly myelodysplasia, and may be useful for detecting clonal myeloid disorders.

Keywords: CD177; Flow cytometry; Myelodysplasia; Neutrophil.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Biological Assay*
  • Biomarkers, Tumor / metabolism
  • Bone Marrow Cells / pathology
  • Child
  • Child, Preschool
  • Clone Cells / pathology
  • Female
  • Flow Cytometry / methods*
  • GPI-Linked Proteins / metabolism
  • Humans
  • Infant
  • Isoantigens / metabolism*
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / diagnosis*
  • Myelodysplastic Syndromes / metabolism
  • Neutrophils / metabolism
  • Neutrophils / pathology*
  • Receptors, Cell Surface / metabolism*
  • Sensitivity and Specificity
  • Young Adult

Substances

  • Biomarkers, Tumor
  • CD177 protein, human
  • GPI-Linked Proteins
  • Isoantigens
  • Receptors, Cell Surface