Expression patterns of CD200 and CD148 in leukemic B-cell chronic lymphoproliferative disorders and their potential value in differential diagnosis

Leuk Lymphoma. 2015;56(12):3329-35. doi: 10.3109/10428194.2015.1030642. Epub 2015 Jun 19.

Abstract

Different combinations of biomarkers analyzed by flow cytometry are critical for the accurate diagnosis of leukemic B-cell chronic lymphoproliferative disorders (B-CLPDs). We investigated CD200 and CD148 expression patterns of blood or bone marrow from 374 cases of B-CLPD by multicolor flow cytometry. Our results showed that CD200 and CD148 expression patterns distinguished different types of B-CLPD. CD200 mean fluorescence intensity (MFI) or CD148 MFI had a high sensitivity and specificity to differentiate mantle cell lymphoma (MCL) from chronic lymphocytic leukemia (CLL). Furthermore, CD148 MFI/CD200 MFI ratio>4.79 produced a specificity of 94.46% (95% confidence interval [CI]: 91.04-96.87%) and a sensitivity of 100% (95% CI: 88.78-100.0%) in establishing the diagnosis of MCL in differential diagnosis between MCL and CLL. We therefore conclude that the combination of CD200 and CD148 may have a potential differential diagnostic value in leukemic B-CLPDs, especially between CLL and MCL.

Keywords: CD148; CD200; Diagnosis; flow cytometry; lymphoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antigens, CD / metabolism*
  • Biomarkers, Tumor*
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / pathology
  • Diagnosis, Differential
  • Female
  • Flow Cytometry
  • Humans
  • Immunophenotyping
  • Leukemia, Lymphocytic, Chronic, B-Cell / diagnosis*
  • Leukemia, Lymphocytic, Chronic, B-Cell / metabolism*
  • Male
  • Middle Aged
  • Receptor-Like Protein Tyrosine Phosphatases, Class 3 / metabolism
  • Sensitivity and Specificity
  • Young Adult

Substances

  • Antigens, CD
  • Biomarkers, Tumor
  • PTPRJ protein, human
  • Receptor-Like Protein Tyrosine Phosphatases, Class 3
  • antigens, CD200