Single cell immune profiling by mass cytometry of newly diagnosed chronic phase chronic myeloid leukemia treated with nilotinib
Language English Country Italy Media print-electronic
Document type Clinical Trial, Journal Article
PubMed
28522574
PubMed Central
PMC5541871
DOI
10.3324/haematol.2017.167080
PII: haematol.2017.167080
Knihovny.cz E-resources
- MeSH
- Single-Cell Analysis methods MeSH
- Fusion Proteins, bcr-abl metabolism MeSH
- Leukemia, Myeloid, Chronic-Phase drug therapy pathology MeSH
- Phosphorylation MeSH
- Leukocytes metabolism MeSH
- Humans MeSH
- Cyclic AMP Response Element-Binding Protein metabolism MeSH
- Pyrimidines pharmacology therapeutic use MeSH
- Signal Transduction drug effects immunology MeSH
- STAT3 Transcription Factor metabolism MeSH
- Protein-Tyrosine Kinases therapeutic use MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Names of Substances
- Fusion Proteins, bcr-abl MeSH
- CREB1 protein, human MeSH Browser
- nilotinib MeSH Browser
- Cyclic AMP Response Element-Binding Protein MeSH
- Pyrimidines MeSH
- STAT3 Transcription Factor MeSH
- Protein-Tyrosine Kinases MeSH
Monitoring of single cell signal transduction in leukemic cellular subsets has been proposed to provide deeper understanding of disease biology and prognosis, but has so far not been tested in a clinical trial of targeted therapy. We developed a complete mass cytometry analysis pipeline for characterization of intracellular signal transduction patterns in the major leukocyte subsets of chronic phase chronic myeloid leukemia. Changes in phosphorylated Bcr-Abl1 and the signaling pathways involved were readily identifiable in peripheral blood single cells already within three hours of the patient receiving oral nilotinib. The signal transduction profiles of healthy donors were clearly distinct from those of the patients at diagnosis. Furthermore, using principal component analysis, we could show that phosphorylated transcription factors STAT3 (Y705) and CREB (S133) within seven days reflected BCR-ABL1IS at three and six months. Analyses of peripheral blood cells longitudinally collected from patients in the ENEST1st clinical trial showed that single cell mass cytometry appears to be highly suitable for future investigations addressing tyrosine kinase inhibitor dosing and effect. (clinicaltrials.gov identifier: 01061177).
Clinic for Hematology University Hospital Sofia Bulgaria
Department of Clinical Chemistry University of Helsinki Finland
Department of Clinical Medicine University of Bergen Norway
Department of Hemato Oncology Stavanger University Hospital Norway
Department of Hematology and Medical Oncology Universitätsklinikum Jena Germany
Department of Hematology Institute of Hematology and Transfusion Medicine Warsaw Poland
Department of Hematology Medical University of Gdańsk Poland
Department of Hematology St Olavs Hospital Trondheim Norway
Department of Hematology University Hospital Center Rebro Zagreb Croatia
Department of Hematology University Hospital Leuven Belgium
Department of Hematology VU University Medical Center Amsterdam the Netherlands
Department of Internal Medicine 4 Wels Grieskirchen Hospital Wels Austria
Department of Internal Medicine Haukeland University Hospital Bergen Norway
Department of Internal Medicine Hematology University Hospital Hradec Kralove Czech Republic
Department of Medicine Karolinska University Hospital Stockholm Sweden
Department of Medicine Oslo University Hospital Norway
Flow Cytometry Facility University of Zurich Switzerland
Hematology Department Cliniques Universitaires St Luc Brussels Belgium
Hematology Unit Aarhus University Hospital Denmark
Internal Medicine Hospital Feldkirch Austria
Mass Cytometry Facility University of Zurich Switzerland
Medical Clinic 3 Oncology Hematology and Rheumatology University Hospital Bonn Germany
Neuroimmunology Lab Haukeland University Hospital Bergen Norway
NMDTI Robert H Lurie Comprehensive Cancer Center of Northwestern University Chicago IL USA
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ClinicalTrials.gov
NCT01061177