4.3 Article

CD34 and CD117 are overexpressed in AML and may be valuable to detect minimal residual disease

Journal

LEUKEMIA RESEARCH
Volume 26, Issue 7, Pages 615-619

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0145-2126(01)00182-5

Keywords

quantitative flow cytometry; minimal residual disease; AML; c-Kit; CD34

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We estimated by quantitative flow cytometry (FC) the expression of CD13, CD33, CD34 and CD 117 antigens in cells from 64 patients with acute myeloid leukaemia (AML) and 22 normal bone marrows (BMs). The method converts fluorescence intensity into number of antigen molecules per cell, measured by antibody binding capacity (ABC). The number of molecules per cell in normal BM was 9.5 +/- 5.7 for CD13, 7 +/- 2.3 for CD33, 6 +/- 0.7 for CD34, and 6.3 +/- 1.5 x 10(3) for CD117. AML blasts expressed 11.4 +/- 12.4 molecules per cell for CD 13, 9.5 +/- 9.7 for CD33, 74 +/- 2328.5 for CD34 and 12.5 +/- 33 x 10(3) for CD117. The number of CD34 and CD117 molecules were significantly higher in AML than in normals (P < 0.0001 and P < 0.05, respectively) while only in a few cases, CD 3 and CD33 were abnormally expressed in myeloblasts. Our results indicate that quantitative analysis of CD34 and CD 117 may be useful to detect minimal residual disease (MRD) and Could be tested in a future to monitor therapy in AML. (C) 2002 Elsevier Science Ltd. All rights reserved.

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