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Characterization of platelet functionality in pediatric patients with kaposiform hemangioendothelioma / Kasabach-Merritt phenomenon
  • +11
  • Alexey Martyanov,
  • Ivan Tesakov,
  • Olga An,
  • Julia-Jessica Korobkin,
  • Anastasia Ignatova,
  • Galina Svidelskaya,
  • Eugenia Yushkova,
  • Ekaterina Koltsova,
  • Nadezhda Podoplelova,
  • Galina Novichkova,
  • Lili Khachatryan,
  • Johannes Eble,
  • Dmitrii Kalinin,
  • Anastasia Sveshnikova
Alexey Martyanov
Dmitry Rogachev National Medical Research Center of Pediatric Hematology Oncology and Immunology

Corresponding Author:[email protected]

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Ivan Tesakov
Dmitry Rogachev National Medical Research Center of Pediatric Hematology Oncology and Immunology
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Olga An
Sechenov University
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Julia-Jessica Korobkin
Center for Theoretical Problems of Physico-Chemical Pharmacology RAS
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Anastasia Ignatova
Dmitry Rogachev National Medical Research Center of Pediatric Hematology Oncology and Immunology
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Galina Svidelskaya
Center for Theoretical Problems of Physico-Chemical Pharmacology RAS
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Eugenia Yushkova
Pirogov Russian National Research Medical University
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Ekaterina Koltsova
Center for Theoretical Problems of Physico-Chemical Pharmacology RAS
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Nadezhda Podoplelova
Center for Theoretical Problems of Physico-Chemical Pharmacology RAS
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Galina Novichkova
Dmitry Rogachev National Medical Research Center of Pediatric Hematology Oncology and Immunology
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Lili Khachatryan
Dmitry Rogachev National Medical Research Center of Pediatric Hematology Oncology and Immunology
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Johannes Eble
University of Münster Institute of Physiological Chemistry and Pathobiochemistry
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Dmitrii Kalinin
University of Münster Department of Chemistry and Pharmacy
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Anastasia Sveshnikova
Center for Theoretical Problems of Physico-Chemical Pharmacology RAS
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Abstract

Background. Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor of infancy commonly associated with Kasabach-Merritt phenomenon (KMP) that includes thrombocytopenia and coagulation dysfunction. Platelet receptor CLEC-2 -tumor cell podoplanin interaction is considered the key mechanism of thrombocytopenia in KMP, however, the effect of long-term exposure to podoplanin on platelet function is unknown.
Procedure. Here we examined blood samples from 7 patients with KHE/KMP. Platelet calcium signaling and functional responses to conventional activation and CLEC-2 stimulation were analyzed by continuous and endpoint live cell flow cytometry. Platelet aggregation in response to ADP or rhodocytin was analyzed by low-angle light scattering approach (LaSca). Additionally, ex vivo thrombus formation on collagen was observed in parallel-plate flow chambers.
Results. We demonstrate that in KHE/KMP platelet functional responses to strong stimulation were on the lower boundary of age-matched normal ranges, while calcium mobilization and fibrinogen binding upon stimulation with ADP alone were significantly lower than control values. Platelet di-aggregate formation in response to ADP was also diminished in most of the patients. Formation of platelet aggregates in collagen-coated parallel plate flow chambers was also noticeably lower than in the age-matched control group. Calcium mobilization in response to CLEC-2 stimulation was unaltered in the patients and could be blocked by low-molecular-weight inhibitors, 2CP and HB125.
 Conclusions. While platelet responsiveness in KHE/KMP is moderately altered, platelet CLEC-2 receptors remain functional and respond to inhibition. Therefore, our findings suggest that CLEC-2-targeting molecules are new potential agents in therapeutic management of this life-threatening condition.