Phenotypic profiling of CD34+ cells by advanced flow cytometry improves diagnosis of juvenile myelomonocytic leukemia
Language English Country Italy Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
37534527
PubMed Central
PMC10828789
DOI
10.3324/haematol.2023.282805
Knihovny.cz E-resources
- MeSH
- Antigens, CD34 genetics MeSH
- Child MeSH
- Leukemia, Myelomonocytic, Juvenile * diagnosis genetics MeSH
- Humans MeSH
- Monocytes pathology MeSH
- Flow Cytometry MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antigens, CD34 MeSH
Diagnostic criteria for juvenile myelomonocytic leukemia (JMML) are currently well defined, however in some patients diagnosis still remains a challenge. Flow cytometry is a well established tool for diagnosis and follow-up of hematological malignancies, nevertheless it is not routinely used for JMML diagnosis. Herewith, we characterized the CD34+ hematopoietic precursor cells collected from 31 children with JMML using a combination of standardized EuroFlow antibody panels to assess the ability to discriminate JMML cells from normal/reactive bone marrow cell as controls (n=29) or from cells of children with other hematological diseases mimicking JMML (n=9). CD34+ precursors in JMML showed markedly reduced B-cell and erythroid-committed precursors compared to controls, whereas monocytic and CD7+ lymphoid precursors were significantly expanded. Moreover, aberrant immunophenotypes were consistently present in CD34+ precursors in JMML, while they were virtually absent in controls. Multivariate logistic regression analysis showed that combined assessment of the number of CD34+CD7+ lymphoid precursors and CD34+ aberrant precursors or erythroid precursors had a great potential in discriminating JMMLs versus controls. Importantly our scoring model allowed highly efficient discrimination of truly JMML versus patients with JMML-like diseases. In conclusion, we show for the first time that CD34+ precursors from JMML patients display a unique immunophenotypic profile which might contribute to a fast and accurate diagnosis of JMML worldwide by applying an easy to standardize single eight-color antibody combination.
Cancer Research Center Salamanca
Centro Tettamanti Fondazione IRCCS San Gerardo dei Tintori Monza
Department of Immunohematology and Blood Transfusion Leiden
Department of Immunology Erasmus MC University Medical Center Rotterdam Rotterdam
Department of Laboratory Medicine Ghent University Hospital Ghent
Department of Pediatric Hematology and Oncology Medical University of Silesia Zabrze
Department of Pediatrics Federal University of Rio de Janeiro Rio de Janeiro
Department of Pediatrics Fondazione IRCCS San Gerardo dei Tintori Monza
Hematology Laboratory CHU de Saint Etienne Saint Etienne Cedex
Institute for Laboratory Medicine Kantonsspital Aarau AG Aarau
Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands
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