Primary MyelofibrosidsNCT07607392
JAK2V617F Mutated Endothelium Has a Stem Cell Potential in Primary Myelofibrosis: a New Disease Ontogenesis for Chronic Myeloproliferative Disorders
An observational study of Primary Myelofibrosids, run by Fondazione IRCCS Policlinico San Matteo di Pavia at 1 site in Italy.
Trial summary
The present project aims to experimentally test the hypothesis that JAK2V617F mutated endothelium in primary myelofibrosis (PMF) we discovered in 2013 represents an embryonic-like hemogenic endothelium and is part of the malignant stem cell pool that give rise to clonal hematopoiesis. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Primary Myelofibrosids
- How many people
- 30 participants
- Where
- 1 siteItaly
- Study dates
- 2 May 2023to 29 Apr 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Healthy volunteers will be enrolled among people working in the Institutions where the project is conducted (San Matteo Foundation and Pavia University in Pavia and IEO in Milan)
Who may be able to join
- availability to understand and sign the informed consent
Who cannot join
- no known concurrent hematologic disease or condition that can affect the interpretation of the results
Trial locations and contacts
1 site in 1 country.
Italy1 site
Fondazione IRCCS Policlinico San Matteo di Pavia
Pavia, Italy, 27100
About this study
The present project aims to experimentally test the hypothesis that JAK2V617F mutated endothelium in primary myelofibrosis (PMF) we discovered in 2013 represents an embryonic-like hemogenic endothelium and is part of the malignant stem cell pool that give rise to clonal hematopoiesis. The hypothesis stems from the recent evidence that JAK2 mutation in PMF patients is acquired in utero or childhood. The experimental plan of the project is 1) to separate mature endothelial cells from peripheral blood of PMF patients for morphological, molecular, functional characterization and clonogenic assays; 2) to assay the megakaryocyte, erythroid, granulocyte and endothelial clonogenic potential of the mature endothelial cells of patients with PMF. The potential to form colonies will be the documentation that a fraction of mature endothelial cells of patients with PMF have the characteristics of embryonic hemogenic endothelium and might act as the cell of origin of PMF.
Read the detailed description
This project stems from our previous original observations that endothelial cells lining the vessel wall of splenic venules and capillaries of PMF patients harbour the JAK2V617F mutation (Piaggio G, Rosti V Blood 2009 and Rosti V Blood 2013) that is found in the hematopoietic cells of patients with myelofibrosis. Subsequently, this finding was further confirmed by other groups (Teofili L Blood 2011 and Farina M Cells 2021), although a definitive agreement on the existence of mutated endothelium in PMF has not been reached and the role of mutated endothelial cells in PMF pathogenesis continues to be questioned.
These observations support the hypothesis that endothelial cells and hematopoietic cells may derive from a common progenitor cell, the hemangioblast, in which the driver mutation(s) arise, thus resulting in mutated endothelial and hematopoietic cells. Whereas in mice evidences that hemangioblast exists have been documented (Fadlullah M Blood 2022), in human a definitive demonstration is still lacking. The demonstration that sorted mature endothelial cells share genetic and functional features with hematopoietic cells and that they retain the capacity to differentiate in culture into hematopoietic progenitor cells will clarify the role and significance of circulating mutated mature endothelial cells in patients with primary myelofibrosis. The significance of the project resides in its novel interpretation of the pathogenesis of PMF and, more in general, of chronic myeloproliferative diseases. The cell of origin of the disease is not anymore identified in a hematopoietic stem/progenitor cell, which acquire a mutation during the adult life and, by its clonal proliferation, results in the development of the disease. In this project the cell of origin of PMF is identified in a cell with hemogenic endothelium potential, that acquires the driver mutation during either fetal or adult life. This cell would give rise to mutated hematopoietic and endothelial cells and, in turn, by its clonal proliferation driven by acquired mutation(s) or an altered microenvironment, to the onset of the disease.
Specific Aim 1 Separation and isolation of mature endothelial cells and hematopoietic progenitor cells from peripheral blood of patients with PMF and normal subjects.
Due to the scant data available in the literature on the frequency of the events that will be investigated in this project, it isnot possible to define a sample size of patients to be included in the study. The Center for the Study of Myelofibrosis at Policlinico San Matteo Foundation assures the accrual of a large number of patients and, in turn, it guarantees that all patients undergoing new diagnostic procedures will be asked to participate to the study. All the procedures will be performed after signing a written informed consent approved by the local IRB of Policlinico San Matteo, Pavia. Peripheral blood samples (20-40 ml) will be obtained from a minimum of 20 patients with a diagnosis of primary myelofibrosis (WHO 2016) and positivity for the JAK2V617F mutation, since this is the most frequently found mutation among the driver mutations in patients. Patients with a previous history of deep vein thrombosis will be included in the study. An equal number of healthy subjects will be used as controls. Hematopoietic progenitor cells (HPCs) and mature endothelial cells will be isolated by sterile cell sorting. Twenty-40 milliliters of PB from patients with PMF or healthy controls will be collected in EDTA tubes; mononuclear cells (MNCs) will be separated by ficoll Hypaque. To allow the sorting of HPCs, half of the MNCs will be stained with the anti-CD45, which will discriminate between the hematopoietic and non hematopoietic cells, and the anti-CD34 monoclonal antibodies. The sorting of circulating mature endothelial cells will be performed by staining the remaining MNCs with endothelial lineage specific markers such as the anti-CD146, also known as the melanoma cell adhesion molecule, and anti-CD105, an endoglin protein expressed by activate endothelial cells, monocytes stromal cells and pre-B cells. The nuclear stain DAPI will be added to all the antibody combination. We expect a purity degree for the sorted cell populations greater than 95%. The sorted HPC and mature circulating endothelial cell populations will be further characterized by molecular studies that will compare by Next Generaation Sequencing (NGS) a panel of myeloidassociated mutations (see below).
Specific Aim 2 Morphological, molecular, and functional characterization of mature circulating endothelial cells in patients with PMF and normal subjects.
Sorted hematopoietic progenitor cells will be characterized by flow cytometry and/or confocal microscopy assessing the CD133, CD117, CD33, CD71, CD14, CD11b, CD41 and CD61 surface antigens. The mature endothelial cells will be characterized by testing the CD144, VEGFR2, CD31 surface antigen expression. In particular, thrombospondin1 and Angiotensin Converting Enzyme expression will be investigated on sorted endothelial cells according with recent observations (Wang Cell Stem Cell 2021 and Fadlullah M Blood 20222, respectively) suggesting that these markers identify cells belonging to the hemogenic endothelium. The genotype will be investigated both on bulk cells and at single cell level by means of the NGS Oncomine Myeloid Research Assay investigating 69 genes/fusion transcripts involved in the pathogenesis of myeloid malignancies. DNA and RNA will be extracted with Maxwell CSC Blood DNA and RNA kit, following the manufacturer¿s instructions. After nucleic acid quantification, we will follow the Oncomine Myeloid procedures (Thermo Fisher Scientific). The genomic and transcript analysis will be performed with an IonReporter software applying the last release of the myeloid workflow. Also, the singlecell RNA expression profile of these cells will be investigated by means of the unbiased 10x Genomics approach described in Falvo et al (Cancer Research 2021) and their phenotype by multiparametric flow cytometry as described in Hu-Lowe et al (Cancer Research 2011). Endothelial cells will also be characterized functionally. This will be done by in vitro tube formation assay (Matrigel assay) by plating mature endothelial cells, re-suspended in complete medium or EBM2 with 2.5% FCS to induce starvation conditions, in plates coated with Cultrex basement membrane extract, a solubilized basement membrane preparation extracted from Engelbreth-Holm-Swarm mouse sarcoma, a tumour rich in extracellular matrix proteins and growth factors.
The total length of tube-like structures will be measured as the ratio of the tube length (mm)/surface of the field (mm2) by ImageJ software (National Institute of Health,USA, http://rsbweb.nih.gov/ij). The main targets of the tasks of this specific aim 2 are represented by a) the characterization of the sorted endothelial and hematopoietic cells and b) the identification of mutations and pathways that are shared between the 2 cell populations, thus confirming their common origin. This in turn will provide evidence that the acquisition of the driver mutation(s) of PMF is an event occurring in a common progenitor cell during human life (possibly during fetal life), able to give origin to both endothelial and hematopoietic lineages.
Specific Aim 3 In vitro assesment of hematopoietic differentiation and clonogenic potential of circulating endothelial cells in patients with PMF.
Cell culture experiments will be performed with the aim to investigate the differentiation and clonogenic hematopioetic potential of endothelial cells isolated from the blood of PMF patients. Clonogenic assays for the in vitro growth of CFU-GEMM, CFU-GM and BFU-E will be set up according with classical semisolid assays. Colonies obtained in these cultures will be characterized at morphological and molecular level as described for sorted cells in Specific Aim 2. With regard to the megakaryocyte lineage, in the last few years, we have set up a protocol to derive megakaryocytes (Mks) from human bone marrow and peripheral blood hematopoietic stem cells. Functional analysis of Mks obtained from our culture system showed that they can extend proplatelets and release functional platelets (PLTs). We plan to exploit our culture methods to differentiate Mks from both hematopoietic progenitors and endothelial cells isolated in Aim 1. To characterize Mks we will assess: a) the expression of CD61 and CD42b by flow cytometry, b) the capacity of forming proplatelets in adhesion to fibrinogen/fibronectin, c) the Thrombopoietin pathway activation by western blot (e.g., pSTAT, pERK, pAKT), d) the expression of different extracellular matrices (e.g., collagen type III, IV, fibronectin) by immunofluorescence imaging and western blot, e) the expression and release of growth factors will be analyzed by different cytokine arrays. Then, we will perform experiments to determine if Mks derived from the two different cell subsets show altered interactions with the extracellular matrix (ECM) components of the bone marrow (BM) microenvironment in terms of changes in morphology, adhesion, and maturation. We will correlate these results with biochemical studies to explore the capacity of Mks to assemble and anchor to the ECM. With these experiments we expect to be able to show the impact of Mks in remodeling matrix components related to the fibrotic BM environment. These experiments will be performed in 2D and then confirmed in our 3D bone marrow model. This 3 D bone marrow model will also be used to assess the capacity of Mks to produce platelets.
- Conditions
- Primary Myelofibrosids
- Keywords
- Primary myelofibrosis, Endothelial cells, JAK2V617F mutation
- Medical subject headings
- Primary Myelofibrosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Patients | Patients affected from primary myelofibrosis | |
| Controls | Healthy subjects whoi volunteer participate to the study |
What is being measured
The primary outcome is the main question the study is designed to answer.
Isolation of endothelial cells
This will be done by cell sorting of peripheral blood samples from both patients and healthy subjects
Measured: from month 1 to month 18
Genotyping of sorted endothelial cells
endothelial cells sorted from patiens or healthy subjects will undergo DNA extraction and assessed for the presence of driver mutations of chronic myeloproliferative diseases
Measured: from month 6 to month 30 of the project
in vito culture of endothelail cells
Sorted endothelial cells will be cultured in vitro in a clonogenic assay in order to obtain differentiation into cells opf the hematopoietic lineage, mainly (but not exclusively megakaryocyte)
Measured: from month 6 to month 36 of the project
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2026
- Study start2 May 2023
- Primary completion28 Feb 2026
- Study completion29 Apr 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for Primary MyelofibrosidsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Fondazione IRCCS Policlinico San Matteo di Pavia
- Sponsor type
- University, hospital or other
- Collaborators
- University of Pavia, IEO Foundation
- Responsible party
- Principal investigator, Vittorio Rosti, Fondazione IRCCS Policlinico San Matteo di Pavia
- Investigators
- Vittorio Rosti, Principal investigator, IRCCS Poiliclinico San Matteo Foundation, Pavia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07607392
- Sponsor's protocol ID
- RF-2021
- Status last verified
- May 2026
- First submitted
- 19 May 2026
- Last updated
- 26 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: IPD are needed for the interpretation of some of the results (in particular genotyping data) but not required for the understanding and interèratation of final results of the study that will be published in aggergate form
Publications
Di Buduo CA, Laurent PA, Zaninetti C, Lordier L, Soprano PM, Ntai A, Barozzi S, La Spada A, Biunno I, Raslova H, Bussel JB, Kaplan DL, Balduini CL, Pecci A, Balduini A. Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients. Elife. 2021 Jun 1;10:e58775. doi: 10.7554/eLife.58775.
PubMed 34059198Fadlullah MZH, Neo WH, Lie-A-Ling M, Thambyrajah R, Patel R, Mevel R, Aksoy I, Do Khoa N, Savatier P, Fontenille L, Baker SM, Rattray M, Kouskoff V, Lacaud G. Murine AGM single-cell profiling identifies a continuum of hemogenic endothelium differentiation marked by ACE. Blood. 2022 Jan 20;139(3):343-356. doi: 10.1182/blood.2020007885.
PubMed 34517413Farina M, Bernardi S, Polverelli N, D'Adda M, Malagola M, Bosio K, Re F, Almici C, Dunbar A, Levine RL, Russo D. Comparative Mutational Profiling of Hematopoietic Progenitor Cells and Circulating Endothelial Cells (CECs) in Patients with Primary Myelofibrosis. Cells. 2021 Oct 15;10(10):2764. doi: 10.3390/cells10102764.
PubMed 34685741Rosti V, Villani L, Riboni R, Poletto V, Bonetti E, Tozzi L, Bergamaschi G, Catarsi P, Dallera E, Novara F, Massa M, Campanelli R, Fois G, Peruzzi B, Lucioni M, Guglielmelli P, Pancrazzi A, Fiandrino G, Zuffardi O, Magrini U, Paulli M, Vannucchi AM, Barosi G; Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative (AGIMM) investigators. Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutation. Blood. 2013 Jan 10;121(2):360-8. doi: 10.1182/blood-2012-01-404889. Epub 2012 Nov 5.
PubMed 23129323Piaggio G, Rosti V, Corselli M, Bertolotti F, Bergamaschi G, Pozzi S, Imperiale D, Chiavarina B, Bonetti E, Novara F, Sessarego M, Villani L, Garuti A, Massa M, Ghio R, Campanelli R, Bacigalupo A, Pecci A, Viarengo G, Zuffardi O, Frassoni F, Barosi G. Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality marker. Blood. 2009 Oct 1;114(14):3127-30. doi: 10.1182/blood-2008-12-190991. Epub 2009 Jul 23.
PubMed 19628707Zambidis ET, Peault B, Park TS, Bunz F, Civin CI. Hematopoietic differentiation of human embryonic stem cells progresses through sequential hematoendothelial, primitive, and definitive stages resembling human yolk sac development. Blood. 2005 Aug 1;106(3):860-70. doi: 10.1182/blood-2004-11-4522. Epub 2005 Apr 14.
PubMed 15831705
Study at a glance
From the registry record, last updated by the sponsor on 26 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- JAK2V617F Mutated Endothelium Has a Stem Cell Potential in Primary Myelofibrosis: a New Disease Ontogenesis for Chronic Myeloproliferative Disorders
- ClinicalTrials.gov ID
- NCT07607392
- Acronym / sponsor ID
- RF-2021
- Conditions
- Primary Myelofibrosids
- Keywords
- Primary myelofibrosis, Endothelial cells, JAK2V617F mutation
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Fondazione IRCCS Policlinico San Matteo di PaviaUniversity, hospital or other
- Collaborators
- University of Pavia, IEO Foundation
- Study start
- 2 May 2023 (actual)
- Primary completion
- 28 Feb 2026 (actual)
- Study completion
- 29 Apr 2026 (actual)
- First posted
- 26 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The present project aims to experimentally test the hypothesis that JAK2V617F mutated endothelium in primary myelofibrosis (PMF) we discovered in 2013 represents an embryonic-like hemogenic endothelium and is part of the malignant stem cell pool that give rise to clonal hematopoiesis. The hypothesis stems from the recent evidence that JAK2 mutation in PMF patients is acquired in utero or childhood. The experimental plan of the project is 1) to separate mature endothelial cells from peripheral blood of PMF patients for morphological, molecular, functional characterization and clonogenic assays; 2) to assay the megakaryocyte, erythroid, granulocyte and endothelial clonogenic potential of the mature endothelial cells of patients with PMF. The potential to form colonies will be the documentation that a fraction of mature endothelial cells of patients with PMF have the characteristics of embryonic hemogenic endothelium and might act as the cell of origin of PMF.
Detailed description
This project stems from our previous original observations that endothelial cells lining the vessel wall of splenic venules and capillaries of PMF patients harbour the JAK2V617F mutation (Piaggio G, Rosti V Blood 2009 and Rosti V Blood 2013) that is found in the hematopoietic cells of patients with myelofibrosis. Subsequently, this finding was further confirmed by other groups (Teofili L Blood 2011 and Farina M Cells 2021), although a definitive agreement on the existence of mutated endothelium in PMF has not been reached and the role of mutated endothelial cells in PMF pathogenesis continues to be questioned.
These observations support the hypothesis that endothelial cells and hematopoietic cells may derive from a common progenitor cell, the hemangioblast, in which the driver mutation(s) arise, thus resulting in mutated endothelial and hematopoietic cells. Whereas in mice evidences that hemangioblast exists have been documented (Fadlullah M Blood 2022), in human a definitive demonstration is still lacking. The demonstration that sorted mature endothelial cells share genetic and functional features with hematopoietic cells and that they retain the capacity to differentiate in culture into hematopoietic progenitor cells will clarify the role and significance of circulating mutated mature endothelial cells in patients with primary myelofibrosis. The significance of the project resides in its novel interpretation of the pathogenesis of PMF and, more in general, of chronic myeloproliferative diseases. The cell of origin of the disease is not anymore identified in a hematopoietic stem/progenitor cell, which acquire a mutation during the adult life and, by its clonal proliferation, results in the development of the disease. In this project the cell of origin of PMF is identified in a cell with hemogenic endothelium potential, that acquires the driver mutation during either fetal or adult life. This cell would give rise to mutated hematopoietic and endothelial cells and, in turn, by its clonal proliferation driven by acquired mutation(s) or an altered microenvironment, to the onset of the disease.
Specific Aim 1 Separation and isolation of mature endothelial cells and hematopoietic progenitor cells from peripheral blood of patients with PMF and normal subjects.
Due to the scant data available in the literature on the frequency of the events that will be investigated in this project, it isnot possible to define a sample size of patients to be included in the study. The Center for the Study of Myelofibrosis at Policlinico San Matteo Foundation assures the accrual of a large number of patients and, in turn, it guarantees that all patients undergoing new diagnostic procedures will be asked to participate to the study. All the procedures will be performed after signing a written informed consent approved by the local IRB of Policlinico San Matteo, Pavia. Peripheral blood samples (20-40 ml) will be obtained from a minimum of 20 patients with a diagnosis of primary myelofibrosis (WHO 2016) and positivity for the JAK2V617F mutation, since this is the most frequently found mutation among the driver mutations in patients. Patients with a previous history of deep vein thrombosis will be included in the study. An equal number of healthy subjects will be used as controls. Hematopoietic progenitor cells (HPCs) and mature endothelial cells will be isolated by sterile cell sorting. Twenty-40 milliliters of PB from patients with PMF or healthy controls will be collected in EDTA tubes; mononuclear cells (MNCs) will be separated by ficoll Hypaque. To allow the sorting of HPCs, half of the MNCs will be stained with the anti-CD45, which will discriminate between the hematopoietic and non hematopoietic cells, and the anti-CD34 monoclonal antibodies. The sorting of circulating mature endothelial cells will be performed by staining the remaining MNCs with endothelial lineage specific markers such as the anti-CD146, also known as the melanoma cell adhesion molecule, and anti-CD105, an endoglin protein expressed by activate endothelial cells, monocytes stromal cells and pre-B cells. The nuclear stain DAPI will be added to all the antibody combination. We expect a purity degree for the sorted cell populations greater than 95%. The sorted HPC and mature circulating endothelial cell populations will be further characterized by molecular studies that will compare by Next Generaation Sequencing (NGS) a panel of myeloidassociated mutations (see below).
Specific Aim 2 Morphological, molecular, and functional characterization of mature circulating endothelial cells in patients with PMF and normal subjects.
Sorted hematopoietic progenitor cells will be characterized by flow cytometry and/or confocal microscopy assessing the CD133, CD117, CD33, CD71, CD14, CD11b, CD41 and CD61 surface antigens. The mature endothelial cells will be characterized by testing the CD144, VEGFR2, CD31 surface antigen expression. In particular, thrombospondin1 and Angiotensin Converting Enzyme expression will be investigated on sorted endothelial cells according with recent observations (Wang Cell Stem Cell 2021 and Fadlullah M Blood 20222, respectively) suggesting that these markers identify cells belonging to the hemogenic endothelium. The genotype will be investigated both on bulk cells and at single cell level by means of the NGS Oncomine Myeloid Research Assay investigating 69 genes/fusion transcripts involved in the pathogenesis of myeloid malignancies. DNA and RNA will be extracted with Maxwell CSC Blood DNA and RNA kit, following the manufacturer¿s instructions. After nucleic acid quantification, we will follow the Oncomine Myeloid procedures (Thermo Fisher Scientific). The genomic and transcript analysis will be performed with an IonReporter software applying the last release of the myeloid workflow. Also, the singlecell RNA expression profile of these cells will be investigated by means of the unbiased 10x Genomics approach described in Falvo et al (Cancer Research 2021) and their phenotype by multiparametric flow cytometry as described in Hu-Lowe et al (Cancer Research 2011). Endothelial cells will also be characterized functionally. This will be done by in vitro tube formation assay (Matrigel assay) by plating mature endothelial cells, re-suspended in complete medium or EBM2 with 2.5% FCS to induce starvation conditions, in plates coated with Cultrex basement membrane extract, a solubilized basement membrane preparation extracted from Engelbreth-Holm-Swarm mouse sarcoma, a tumour rich in extracellular matrix proteins and growth factors.
The total length of tube-like structures will be measured as the ratio of the tube length (mm)/surface of the field (mm2) by ImageJ software (National Institute of Health,USA, http://rsbweb.nih.gov/ij). The main targets of the tasks of this specific aim 2 are represented by a) the characterization of the sorted endothelial and hematopoietic cells and b) the identification of mutations and pathways that are shared between the 2 cell populations, thus confirming their common origin. This in turn will provide evidence that the acquisition of the driver mutation(s) of PMF is an event occurring in a common progenitor cell during human life (possibly during fetal life), able to give origin to both endothelial and hematopoietic lineages.
Specific Aim 3 In vitro assesment of hematopoietic differentiation and clonogenic potential of circulating endothelial cells in patients with PMF.
Cell culture experiments will be performed with the aim to investigate the differentiation and clonogenic hematopioetic potential of endothelial cells isolated from the blood of PMF patients. Clonogenic assays for the in vitro growth of CFU-GEMM, CFU-GM and BFU-E will be set up according with classical semisolid assays. Colonies obtained in these cultures will be characterized at morphological and molecular level as described for sorted cells in Specific Aim 2. With regard to the megakaryocyte lineage, in the last few years, we have set up a protocol to derive megakaryocytes (Mks) from human bone marrow and peripheral blood hematopoietic stem cells. Functional analysis of Mks obtained from our culture system showed that they can extend proplatelets and release functional platelets (PLTs). We plan to exploit our culture methods to differentiate Mks from both hematopoietic progenitors and endothelial cells isolated in Aim 1. To characterize Mks we will assess: a) the expression of CD61 and CD42b by flow cytometry, b) the capacity of forming proplatelets in adhesion to fibrinogen/fibronectin, c) the Thrombopoietin pathway activation by western blot (e.g., pSTAT, pERK, pAKT), d) the expression of different extracellular matrices (e.g., collagen type III, IV, fibronectin) by immunofluorescence imaging and western blot, e) the expression and release of growth factors will be analyzed by different cytokine arrays. Then, we will perform experiments to determine if Mks derived from the two different cell subsets show altered interactions with the extracellular matrix (ECM) components of the bone marrow (BM) microenvironment in terms of changes in morphology, adhesion, and maturation. We will correlate these results with biochemical studies to explore the capacity of Mks to assemble and anchor to the ECM. With these experiments we expect to be able to show the impact of Mks in remodeling matrix components related to the fibrotic BM environment. These experiments will be performed in 2D and then confirmed in our 3D bone marrow model. This 3 D bone marrow model will also be used to assess the capacity of Mks to produce platelets.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Patients | – | –Patients affected from primary myelofibrosis |
| Controls | – | –Healthy subjects whoi volunteer participate to the study |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Healthy volunteers will be enrolled among people working in the Institutions where the project is conducted (San Matteo Foundation and Pavia University in Pavia and IEO in Milan)
Key inclusion criteria (1 listed)
- availability to understand and sign the informed consent
Key exclusion criteria (1 listed)
- no known concurrent hematologic disease or condition that can affect the interpretation of the results
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Isolation of endothelial cells
Time frame: from month 1 to month 18
This will be done by cell sorting of peripheral blood samples from both patients and healthy subjects
Genotyping of sorted endothelial cells
Time frame: from month 6 to month 30 of the project
endothelial cells sorted from patiens or healthy subjects will undergo DNA extraction and assessed for the presence of driver mutations of chronic myeloproliferative diseases
in vito culture of endothelail cells
Time frame: from month 6 to month 36 of the project
Sorted endothelial cells will be cultured in vitro in a clonogenic assay in order to obtain differentiation into cells opf the hematopoietic lineage, mainly (but not exclusively megakaryocyte)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 May 2026.
- Background: PubMed 34059198Di Buduo CA, Laurent PA, Zaninetti C, Lordier L, Soprano PM, Ntai A, Barozzi S, La Spada A, Biunno I, Raslova H, Bussel JB, Kaplan DL, Balduini CL, Pecci A, Balduini A. Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients. Elife. 2021 Jun 1;10:e58775. doi: 10.7554/eLife.58775.
- Background: PubMed 34517413Fadlullah MZH, Neo WH, Lie-A-Ling M, Thambyrajah R, Patel R, Mevel R, Aksoy I, Do Khoa N, Savatier P, Fontenille L, Baker SM, Rattray M, Kouskoff V, Lacaud G. Murine AGM single-cell profiling identifies a continuum of hemogenic endothelium differentiation marked by ACE. Blood. 2022 Jan 20;139(3):343-356. doi: 10.1182/blood.2020007885.
- Background: PubMed 34685741Farina M, Bernardi S, Polverelli N, D'Adda M, Malagola M, Bosio K, Re F, Almici C, Dunbar A, Levine RL, Russo D. Comparative Mutational Profiling of Hematopoietic Progenitor Cells and Circulating Endothelial Cells (CECs) in Patients with Primary Myelofibrosis. Cells. 2021 Oct 15;10(10):2764. doi: 10.3390/cells10102764.
- Background: PubMed 23129323Rosti V, Villani L, Riboni R, Poletto V, Bonetti E, Tozzi L, Bergamaschi G, Catarsi P, Dallera E, Novara F, Massa M, Campanelli R, Fois G, Peruzzi B, Lucioni M, Guglielmelli P, Pancrazzi A, Fiandrino G, Zuffardi O, Magrini U, Paulli M, Vannucchi AM, Barosi G; Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative (AGIMM) investigators. Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutation. Blood. 2013 Jan 10;121(2):360-8. doi: 10.1182/blood-2012-01-404889. Epub 2012 Nov 5.
- Background: PubMed 19628707Piaggio G, Rosti V, Corselli M, Bertolotti F, Bergamaschi G, Pozzi S, Imperiale D, Chiavarina B, Bonetti E, Novara F, Sessarego M, Villani L, Garuti A, Massa M, Ghio R, Campanelli R, Bacigalupo A, Pecci A, Viarengo G, Zuffardi O, Frassoni F, Barosi G. Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality marker. Blood. 2009 Oct 1;114(14):3127-30. doi: 10.1182/blood-2008-12-190991. Epub 2009 Jul 23.
- Background: PubMed 15831705Zambidis ET, Peault B, Park TS, Bunz F, Civin CI. Hematopoietic differentiation of human embryonic stem cells progresses through sequential hematoendothelial, primitive, and definitive stages resembling human yolk sac development. Blood. 2005 Aug 1;106(3):860-70. doi: 10.1182/blood-2004-11-4522. Epub 2005 Apr 14.
- Individual participant dataSharing planned: No. IPD are needed for the interpretation of some of the results (in particular genotyping data) but not required for the understanding and interèratation of final results of the study that will be published in aggergate form
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Vittorio Rosti principal investigator
IRCCS Poiliclinico San Matteo Foundation, Pavia
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Primary Myelofibrosids, run by Fondazione IRCCS Policlinico San Matteo di Pavia at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Isolation of endothelial cells (time frame: from month 1 to month 18). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07607392, which also lists 6 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 May 2026.