CD158k and PD-1 expressions define heterogeneous subtypes of Sezary syndrome

Author:

Vergnolle Inès1,Douat-Beyries Claudia1,Boulinguez Serge2,Rieu Jean-Baptiste3ORCID,Vial Jean Philippe4ORCID,Baracou Rolande1,Boudot Sylvie1,Cazeneuve Aurore1,Chaugne Sophie1,Durand Martine1,Estival Sylvie1,Lablanche Nicolas1,Nicolau-Travers Marie-Laure1,Tournier Emilie5,Lamant Laurence6,Vergez Francois7ORCID

Affiliation:

1. CHU Toulouse -IUCT, Toulouse, France

2. CHU Toulouse Larrey, Toulouse, France

3. Institut Universitaire du Cancer - Oncopole, Toulouse, France

4. Bordeaux University Hospital, pessac, Georgia, France

5. CHU Toulouse, Toulouse, France

6. Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France

7. IUCT, Toulouse, France

Abstract

Sezary syndrome (SS) is a rare leukemic form of cutaneous T-cell lymphoma. Diagnosis mainly depends on flow cytometry, but results are not specific enough to be unequivocal. The difficulty in defining a single marker that could characterize Sezary cells may be the consequence of different pathological subtypes. In this study, we used multivariate flow cytometry analyses. We chose to investigate the expression of classical CD3, CD4, CD7, and CD26 and the 2 new association of 2 markers CD158k and PD-1. We performed lymphocyte computational phenotypic analyses during diagnosis and follow-up of SS patients to define new SS classes and improve the sensitivity of the diagnosis and the follow-up flow cytometry method. Three classes of SS, defined by different immunophenotypic profiles, CD158k-positive SS, CD158k-negative PD-1-positive SS, CD158k and PD-1 double-negative SS, showed different CD8+ and B-cells environments. Such a study could help to diagnose and define biological markers of susceptibility/resistance to treatment including immunotherapy. -

Publisher

American Society of Hematology

Subject

Hematology

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