Absence of CD26 expression is a useful marker for diagnosis of T-cell lymphoma in peripheral blood

Am J Clin Pathol. 2001 Jun;115(6):885-92. doi: 10.1309/U1Y6-J4AG-5M4M-7AYV.

Abstract

We report flow cytometric characterization of surface CD26 expression in 271 peripheral blood samples from 154 patients evaluated for the presence of a T-cell lymphoproliferative disorder, primarily mycosis fungoides/Sézary syndrome (MF/SS). The presence of morphologically identifiable tumor cells on peripheral blood smears was the criterion for lymphomatous involvement. In 66 of 69 samples from 28 patients, we identified an abnormal CD26-/dim T-cell population that was distinct from the variable CD26 expression seen in normal peripheral blood T cells. This population was CD26- in 23 patients and weakly CD26+ in 5 patients. CD7 was more variably expressed in MF/SS tumor cells, allowing recognition of a distinct, quantifiable abnormal T-cell population in only 34 of 69 involved samples. An increased CD4/CD8 ratio and lower surface expression of CD4 in tumor cells also helped separate the CD26-/dim atypical population for quantification. In 35 blood samples from other types of T-cell tumors, tumor cells in 10 of 11 morphologically involved cases showed absent/dim CD26. Although capable of detecting abnormalities in most cases of MF/SS, CD7 expression does not provide as clear a separation of the neoplastic population and can be replaced by CD26 staining in routine peripheral blood flow cytometric screening of MF/SS patients.

Publication types

  • Evaluation Study

MeSH terms

  • Antigens, CD7 / blood
  • Antigens, Differentiation, T-Lymphocyte / blood
  • Biomarkers, Tumor / blood*
  • Dipeptidyl Peptidase 4 / blood*
  • Flow Cytometry
  • Humans
  • Lymphoma, T-Cell / blood
  • Lymphoma, T-Cell / diagnosis
  • Lymphoproliferative Disorders / blood
  • Mycosis Fungoides / blood
  • Mycosis Fungoides / diagnosis*
  • Sezary Syndrome / blood
  • Sezary Syndrome / diagnosis*
  • T-Lymphocyte Subsets / classification

Substances

  • Antigens, CD7
  • Antigens, Differentiation, T-Lymphocyte
  • Biomarkers, Tumor
  • Dipeptidyl Peptidase 4