Evaluation of Sézary cell marker expression and cell death behaviour upon in vitro treatment by flow cytometry in Sézary syndrome patients

Author:

Melchers S.123ORCID,Roemer M.4ORCID,Albrecht J. D.123,Assaf C.5,von Gugelberg C.6,Guenova E.7ORCID,Klemke C.‐D.8,Moritz R. K. C.910,Schlaak M.11,Stadler R.12ORCID,Wehkamp U.13ORCID,Wobser M.14ORCID,Albrecht T.15,Goerdt S.1,Schneider S.4,Nicolay J. P.123ORCID

Affiliation:

1. Department of Dermatology, Venereology and Allergology University Medical Center Mannheim/University of Heidelberg Mannheim Germany

2. Skin Cancer Unit German Cancer Research Center (DKFZ) Heidelberg Germany

3. Section of Clinical and Experimental Dermatology, Medical Faculty Mannheim University of Heidelberg Mannheim Germany

4. Institute for Clinical Chemistry and Laboratory Medicine University Medical Center Mannheim, Ruprecht‐Karls‐University of Heidelberg Mannheim Germany

5. Department of Dermatology HELIOS Klinik Krefeld Krefeld Germany

6. Department of Dermatology University Hospital Zurich Zurich Switzerland

7. Department of Dermatology Lausanne University Hospital Lausanne Switzerland

8. Department of Dermatology, Municipal Medical Center Karlsruhe Teaching Hospital of the University of Freiburg Freiburg Germany

9. Department of Dermatology University Hospital Halle Halle Germany

10. Department of Dermatology, Venerology and Allergology Freie Universität Berlin and Humboldt‐Universität zu Berlin, University Medical Centre Berlin Berlin Germany

11. Department of Dermatology University Hospital Munich Munich Germany

12. Department of Dermatology Johannes‐Wesling‐Clinic Minden and University of Bochum Bochum Germany

13. Department of Dermatology University Hospital Kiel Kiel Germany

14. Department of Dermatology University Hospital Wurzburg Wurzburg Germany

15. Department of Pathology Ruprechts‐Karls‐University of Heidelberg Heidelberg Germany

Abstract

AbstractThe diagnosis of Sézary syndrome (SS) relies on the identification of blood Sézary cells (SC) by different markers via flow cytometry. Treatment of SS is challenging since its pathogenesis is characterized by cell death resistance rather than hyperproliferation. In this study, we establish an integrated approach that considers both the expression of SC markers and sensitivity to cell death both spontaneously and upon in vitro treatment. Peripheral blood mononuclear cells were isolated from 20 SS patients and analysed for the SC markers CD7 and CD26 loss as well as CD158k and PD1 gain. The cells were then treated with different established and experimental therapies in vitro and cell death was measured. Spontaneous and therapeutically induced cell death were measured and correlated to cellular marker profiles. In the marker‐positive cells, spontaneous cell death sensitivity was reduced. Different treatments in vitro managed to specifically induce cell death in the putative CTCL cell populations. Interestingly, a repeated analysis after 3 months of treatment revealed the CTCL cell death sensitivity to be restored by therapy. We propose this novel integrated approach comprising the evaluation of SC marker expression and analysis of cell death sensitivity upon treatment that can also enable a better therapy stratification.

Funder

Deutsche Forschungsgemeinschaft

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

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