Splenic TFH expansion participates in B-cell differentiation and antiplatelet-antibody production during immune thrombocytopenia

Author:

Audia Sylvain123,Rossato Marzia1,Santegoets Kim1,Spijkers Sanne1,Wichers Catharina1,Bekker Cornelis1,Bloem Andries1,Boon Louis4,Flinsenberg Thijs1,Compeer Ewoud1,van den Broek Theo1,Facy Olivier5,Ortega-Deballon Pablo5,Berthier Sabine3,Leguy-Seguin Vanessa3,Martin Laurent26,Ciudad Marion2,Samson Maxime2,Trad Malika2,Lorcerie Bernard3,Janikashvili Nona2,Saas Philippe2,Bonnotte Bernard23,Radstake Timothy R. D. J.1

Affiliation:

1. Laboratory of Translational Immunology, University Medical Center, Utrecht, The Netherlands;

2. Centre de Recherche INSERM 1098, University of Bourgogne/Franche-Comté, Fédération Hospitalo-Universitaire Integrated Center for Research in Inflammatory Diseases, Bourgogne, France;

3. Department of Internal Medicine and Clinical Immunology, Competence Center for Autoimmune Cytopenia, University Hospital, Dijon, France;

4. Bioceros, Utrecht, The Netherlands; and

5. Department of Surgery and

6. Department of Pathology, University Hospital, Dijon, France

Abstract

Key Points Human splenic TFH expansion during ITP participates in B-cell differentiation and antiplatelet-antibody production. IL-21 and CD40 are key TFH molecules that could be promising targets in the treatment of ITP.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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