Thrombocytopenic disorders have been treated with the Thrombopoietin-receptor agonist Eltrombopag. Patients with the same apparent form of thrombocytopenia may respond differently to the treatment. We describe a miniaturized bone marrow tissue model that provides a screening bioreactor for personalized, pre-treatment response prediction to Eltrombopag for individual patients. Using silk fibroin, a 3D bone marrow niche was developed that reproduces platelet biogenesis. Hematopoietic progenitors were isolated from a small amount of peripheral blood of patients with mutations in ANKRD26 and MYH9 genes, who had previously received Eltrombopag. The ex vivo response was strongly correlated with the in vivo platelet response. Induced Pluripotent Stem Cells (iPSCs) from one patient with mutated MYH9 differentiated into functional megakaryocytes that responded to Eltrombopag. Combining patient-derived cells and iPSCs with the 3D bone marrow model technology allows having a reproducible system for studying drug mechanisms and for individualized, pre-treatment selection of effective therapy in Inherited Thrombocytopenias.

Miniaturized 3d bone marrow tissue model to assess response to thrombopoietin-receptor agonists in patients

Di Buduo C. A.;Zaninetti C.;Soprano P. M.;Barozzi S.;Pecci A.;Balduini A.
2021-01-01

Abstract

Thrombocytopenic disorders have been treated with the Thrombopoietin-receptor agonist Eltrombopag. Patients with the same apparent form of thrombocytopenia may respond differently to the treatment. We describe a miniaturized bone marrow tissue model that provides a screening bioreactor for personalized, pre-treatment response prediction to Eltrombopag for individual patients. Using silk fibroin, a 3D bone marrow niche was developed that reproduces platelet biogenesis. Hematopoietic progenitors were isolated from a small amount of peripheral blood of patients with mutations in ANKRD26 and MYH9 genes, who had previously received Eltrombopag. The ex vivo response was strongly correlated with the in vivo platelet response. Induced Pluripotent Stem Cells (iPSCs) from one patient with mutated MYH9 differentiated into functional megakaryocytes that responded to Eltrombopag. Combining patient-derived cells and iPSCs with the 3D bone marrow model technology allows having a reproducible system for studying drug mechanisms and for individualized, pre-treatment selection of effective therapy in Inherited Thrombocytopenias.
2021
Experimental Biology covers a wide array of topics concerned with research in general biology and biological systems, including evolution, ecology, radiation biology, anatomy, general biology, and resources containing diverse topics in basic biology research. Resources on general biomedicine are excluded and are covered in the Medical Research: General Topics category. Resources with strong reliance on fields that fall outside of the core topics of Life sciences, such as biomedical engineering are placed in the Multidisciplinary category.
Medical Research, General Topics covers a wide array of topics in medical and biomedical research, with a specific emphasis on human disease, human tissues, and all levels of research into the pathogenesis of clinically significant conditions. Specific medical fields that are characterized by the inclusion of material from several other specializations are also covered here; these include general and internal medicine, tropical medicine, pediatrics, gerontology, epidemiology, and public health. Resources dealing with specific clinical interventions are excluded and are placed in the Medical Research: Diagnosis & Treatment category. Resources that emphasize the specific disease types, or specific systems affected are also excluded and are categorized according to the pathogen or system pathophysiology.
Esperti anonimi
Inglese
Internazionale
ELETTRONICO
10
30
Induced Pluripotent Stem Cell; Inherited Thrombocytopenia; bone marrow; human; medicine; megakaryocyte; silk; thrombopoietin
https://elifesciences.org/articles/58775
15
info:eu-repo/semantics/article
262
Di Buduo, C. A.; Laurent, P. -A.; Zaninetti, C.; Lordier, L.; Soprano, P. M.; Ntai, A.; Barozzi, S.; La Spada, A.; Biunno, I.; Raslova, H.; Bussel, J....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1438501
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