Identification of the Ki-1 antigen (CD30) as a novel therapeutic target in systemic mastocytosis

Author:

Blatt Katharina1,Cerny-Reiterer Sabine12,Schwaab Juliana3,Sotlar Karl4,Eisenwort Gregor2,Stefanzl Gabriele1,Hoermann Gregor5,Mayerhofer Matthias6,Schneeweiss Mathias17,Knapp Sylvia78,Rülicke Thomas9,Hadzijusufovic Emir1210,Bauer Karin1,Smiljkovic Dubravka1,Willmann Michael10,Reiter Andreas3,Horny Hans-Peter4,Valent Peter12

Affiliation:

1. Department of Internal Medicine I, Division of Hematology and Hemostaseology and

2. Ludwig Boltzmann Cluster Oncology, Medical University of Vienna, Vienna, Austria;

3. Department of Hematology and Oncology, University Hospital Mannheim, Mannheim, Germany;

4. Institute of Pathology, Ludwig-Maximilians-University, Munich, Germany;

5. Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria;

6. Department of Laboratory Medicine, Hanusch Hospital, Vienna, Austria;

7. Department of Internal Medicine I, Laboratory of Infection Biology, Medical University of Vienna, Vienna, Austria;

8. Research Center for Molecular Medicine (CeMM) of the Austrian Academy of Sciences, Vienna, Austria; and

9. Institute of Laboratory Animal Science and

10. Department/Clinic for Companion Animals and Horses, Clinic for Small Animals, Clinical Unit of Internal Medicine, University of Veterinary Medicine, Vienna, Austria

Abstract

Key Points In a majority of patients with advanced SM, neoplastic MCs express the target receptor CD30. The CD30-targeting drug brentuximab-vedotin blocks growth and survival in CD30+ neoplastic MCs which favors drug development in advanced SM.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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