Hybride Ontmoetingsdag Amyloïdose 2024

programma

• 10:00 – 10:30 uur

  Ontvangst met koffie en thee in De Schakel Nijkerk

• 10:30 – 10:40 uur

  Welkom door John Rusman, bestuur Amyloïdose Nederland
  

• 10:40 – 10:45 uur

  Oprichting van en samenwerking met Amybel, Guy Lippens, Amyloïdose België

• 10:45 uur

  Wisselen van zaal voor deelnemers aan ATTR presentatie

• 10:55 – 11:40 uur

  ATTR amyloïdose, update van de laatste ontwikkelingen en beantwoorden van vragen
  Dr. Hans Nienhuis, internist-allergoloog/immunoloog, UMC Groningen

• 10:55 – 11:40 uur

  AL amyloïdose, update van de laatste ontwikkelingen en beantwoorden van vragen
  Prof.dr. Monique Minnema, internist-hematoloog, UMC Utrecht

• 11:40 – 11:50 uur

  Deelnemers van ATTR presentatie gaan terug naar plenaire zaal

• 11:50 – 12:35 uur

  Ontwikkelingen bij nierproblemen en beantwoorden van vragen
  Dr. Alferso Abrahams, internist-nefroloog, UMC Utrecht

• 12:35 – 14:00 uur

  Lunchpauze voor de deelnemers in Nijkerk en tijd voor ontmoeting

• 14:00 – 15:00 uur

  Lotgenotencontact (niet online te volgen)
  U gaat in gesprek en kunt ervaringen delen met lotgenoten.
  Dit gebeurt in groepen van max. 15 personen.

• 15:00 – 16:00 uur

  Gelegenheid tot napraten onder het genot van een hapje en drankje

Inschrijving

program

• 15:00 – 16:00

  Outward journey Holwerd-Nes

• 16:45 – 17:30

  • Check-in hotel

• 18:30 – 19:30

  Cell cycle structure and speed in erythroid development and the response to erythroid stress
  Merav Socolovsky, Professor UMASS Chan Medical School, United States

• 19:30 – 21:30

  Buffet dinner

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Scientific session 1 – Erythropoiesies

Chairs:  Wassim el Nemer / Catarina Freire 

• 09:00 – 09:30

  Erythromyeloblastic Islands
  Lionel Blanc, Northwell, United States

• 09:30 – 09:45

  Anemia links β-catenin with FOXO3 signaling during erythroid terminal differentiation
  Santhe van der Meulen, Sanquin, the Netherlands

• 09:45 – 10:00

  In vitro culture of erythroblasts (EBL) and production of mature erythrocytes for transfusions requires upscaling in fluidic-turbulent systems
  Giulia Iacono, Sanquin, the Netherlands

• 10:00 – 10:15

  The Role of the Zcchc6/Dis3L2 RNA Editor-Exonuclease Axis in Terminal Erythroid Differentiation
  Areum Han, Harvard Medical school / Boston’s Children Hospital, United States

• 10:15 – 10:30

  Transfusion-ready red blood cell generation from induced pluripoten stem cells (iPSCs)
  Emile van den Akker, Sanquin, the Netherlands

• 10:30 – 10:45

  Detailed characterization of iPSC-derived hematopoiesis and erythropoiesis en self-organized cellular complexes (hemanoids)
  Isabel Dorn, Medical University Graz, Austria

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Scientific session 2 – Ion channels of the red blood cell – function and disorders

Chairs: Giampaolo Minetti /  Silvia Neri

• 11:15 – 11:45

  Defects of RBC cell volume regulation and hydration state: their pathophysiology and diagnosis
  Paola Bianchi, Fondazione IRCCS Ca’ Granda Policlinico Milan, Italy

• 11:45 – 12:00

  Electrophysiological characterization of red blood cells using the automated patch clamp
  Nicoletta Muarciano, Nanion Technologies, Germany

• 12:00 – 12:15

  Role of Piezo 1 in terminal density reversal of healthy red blood cells
  Kuntal Dey, University of Zurich, Switserland

• 12:15 – 12:30

  Red Blood Cell Protein contribution to Malaria Parasite Invasion. Basigin mediation of Plasmodium falciparum red blood cell invasion does not require its transmembrane domain or interaction with monocarboxylate transporter
  Timothy Satchwell, University Bristol, UK
  

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• 12:30

  Lunch
  

• Networking session

• Poster presentations – titles and authors can be found below this program

• ‘Meet the expert’ session with Ingolf Bernhardt
  Unsolved problems in red cell research
  Ingolf Bernhardt, University Saarland, Germany

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Scientific session 3 – Red blood cell membrane and associated disorders  & 4. Clinical hematology – new treatments in sickle cell disease and other hereditary red blood cell disorders

Chairs: Stephane Egee / Min Qiao

Red blood cell membrane and associated disorders

• 16:00 – 16:30

  Membranopathies : from cytology and red cell/reticulocyte indices to molecular diagnosis, including prenatal diagnosis
  Lydie da Costa, University Paris, France

• 16:30 – 16:45

  Developmental changes in membrane lipid composition during terminal maturation of circulating human reticulocytes and ageing of red cells
  Giampaolo Minetti, University of Pavia, Italy

• 16:45 – 17:00

  Modulation of terminal erythropoiesis by a TSPO ligand
  Alice Dussouchaud, Inserm, France

• 17:00 – 17:15

  Complete absence of GLUT1 does not impair human terminal erythroid differentiation
  Catarina Freire, University of Bristol, United Kingdom

• 17:15 – 17:30

  Dual action of Dooku1 on PIEZO1 channel in human red blood cells
  Guillaume Bouyer, CNRS, France

Clinical hematology – new treatments in sickle cell disease and other hereditary red blood cell disorders

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Scientific session 4 – Clinical hematology – new treatments in sickle cell disease and other hereditary red blood cell disorders

Chairs: Sjaak Philipsen / Marissa Traets

• 09:00 – 09:30

  Curative approaches for patients with sickle cell disease
  Erfan Nur, Amsterdam UMC, the Netherlands

• 09:30 – 09:45

  Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sickling
  Nicolas Hebert, Etablissement Francais Du Sand, France

• 09:45 – 10:00

  Metabolic blood profile and response to treatment with the pyruvate kinase activator mitapivat in patients with sickle cell disease
  Myrthe van Dijk, UMC Utrecht, the Netherlands

• 10:00 – 10:15

  Plasma Proteome Profiling of Sickle Cell Patients Reveals Activation of Inflammatory Pathways During Steady State and Vaso-occlusive Crisis
  Lydian de Ligt, Amsterdam UMC, the Netherlands

• 10:15 – 10:30

  Red cell rheology and blood viscosity in individuals with sickle cell disease following allogenic bone marrow transplantation or autologous gene addition therapy
  Vivien Sheehan, Emory University of Medicine, United States

• 10:30 – 10:45

  A novel allosteric activator of pyruvate kinase enhances human and mouse enzymatic activity and leads to ematological improvements in sickle cell disease mouse models
  Carsten Alt, Pfizer

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Scientific session 5 – Disorders of Erythropoiesies

Chairs: Tim Satchwell / Carolina Hernandez

• 11:15 – 11:45

  Patient-specific cell lines to study erythropoiesis and hemoglobin switching
  Sjaak Philipsen, Erasmus MC Rotterdam, the Netherlands

• 11:45 – 12:00

  Ineffective erythropoiesis negatively impacts the erythroblastic island in sickle cell disease
  Wassim El Nemer, EFS Sante, France

• 12:00 – 12:15

  Anemia in aged mice is accompanied by reduced erythroid lineage cell production and increased red blood cell life span
  Carsten Alt, Pfizer, United States

• 12:15 – 12:30

  Development of a beta-thalassemia rat model for bone marrow characterization after stem cell transplantation
  Karolin Roemhild, Sanquin, the Netherlands
  

• 12:30 – 12:45

  Elucidating glucocorticoid-responsiveness in Diamond-Blackfan anemia syndrome using iPSC-derived erythroblasts
  Teun Slijkerman, Sanquin, the Netherlands

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Sponsored session

• 12:45 – 13:00

  Lorrca Developments
  Presentation by Pim Brandjes, RR Mechatronics

• 13:00 – 13:15

  RoxyScan: a novel method to evaluate red blood cell resilience to oxidative stress exposure in Sickle Cell disease
  Carolina Hernandez, University Medical Center Utrecht, The Netherlands

• 13:15 – 13:30

  Getinge

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Scientific session 6 – New developments for red cell research  and diagnostics

Chairs: Paola Bianchi / Jonathan de Wilde

• 09:00 – 09:30

  Probing red blood cells’s bio-mechanical properties
  Lars Kaestner, University of Saarland, Germany

• 09:30 – 09:45

  An Efficient and Specific Reporter System Suitable for High-Throughput Screening of Novel Fetal Hemoglobin Inducers
  Tingyue Li, ErasmusMC,  Rotterdam, the Netherlands

• 09:45 – 10:00

  Pyruvate Kinase Thermostability Is Associated with Red Blood Cell Adhesion, Deformability and Oxygen Affinity in Patients with Sickle Cell Disease
  Marissa Traets, UMC Utrecht, the Netherlands

• 10:00 – 10:15

  Towards quantification of intracellular free calcium in individual red blood cells by fluorescence lifetime imaging microscopy
  Min Qiao, Saarland University, Germany

• 10:15 – 10:30

  Ex vivo glycolytic flux measurements in red blood cells
  Titine Ruiter, UMC Utrecht, the Netherlands

• 10:30 – 10:45

  Hepatic Leukemia Factor as a marker for iPSC – derived Hematopoietic Stem Cells
  Maria Simanovich, Erasmus MC Rotterdam, the Netherlands

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Scientific session 7 – New developments for red cell research and diagnostics & 6. New developments for red cell research and diagnostics

Chairs: Lars Kaestner / Giulia Iacono

Clinical cases

New developments for red cell research and diagnostics

• 11:45 – 12:00

  An AI-based imaging flow cytometry approach to study erythrophagocytosis
  Silvia Neri, Sanquin, the Netherlands

• 12:00 – 12:15

  Endothelialized 3D perfusion model to study ex vivo reticulocyte-to-erythrocyte transition
  Claudia Maria Bernecker, University of Graz, Austria

• 12:15 – 12:30

  Actomyosin-driven expulsion of hemoglobin during hemolysis,
  Tessa Korsa, Fraunhofer IBMT, Sulzbach, Germany

• 12:30 – 12:45

  Red cell function devices under development for use in sickle cell disease
  Vivien Sheehan, Emory University School of Medicine, Atlanta, United States

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Scientific session 8 – Clinical hematology – new diagnostic approaches & 2. Ion Channels

Chairs: Vivian Sheehan / Myrthe van Dijk

• 13:45 – 14:15

  Biomarkers in sickle cell disease
  Minke Rab, UMC Utrecht, The Netherlands

• 14:15 – 14:30

  Novel direct plasma heme-related assay decyphers hemolytic anemia and ineffective erythropoiesis
  Nicolas Hebert, Etablissement Francais Du Sang IDF, France

• 14:30 – 14:45

  Impact of Sickle Cell Disease Patients-Derived Red Blood Cells on Clot Dynamics and Fibrin Structure
  Naoual Ouazzani Chahdi, Sanquin, the Netherlands
  

• 14:45 – 15:00

  Low Voxelotor Concentrations Exacerbate Sickle Cell Formation At Low Oxygen Pressure
  Emile van den Akker, Sanquin, the Netherlands

• 15:00 – 15:15

  Soluble Transferrin Receptor as a Marker for Assessing Disease Severity in  Hereditary Hemolytic Anemias
  Geoffrey Kuppens, UMC Utrecht, the Netherlands
  Presented by Marije Bartels, UMC Utrecht, the Netherlands

• 15:15 – 15:30

  Autoimmune hemolytic anemia anti-RBC IgM, but not IgG, drive in vitro complement activation
  Femke Mulder, Sanquin, the Netherlands

Ion Channels

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• 15:45 – 16:15

  Coffee break, followed by sessions:
  

• 15:45 – 16:45

  Poster presentations – titles and authors can be found under this program

• 15:45 – 17:00

  Steering Committee meeting on the consensus-based Recommendation for the Diagnosis of Rare Hemolytic Anemia
  Sponsored by EuroBloodNet

• 17:00 – 17:45

  ERCS General Assembly meeting 

• 18:30 – 21:30

  Dinner

• 07:00 – 08:00

  Breakfast and checkout, payment of expenses (bar)

• 08:30

  Departure from hotel by bus to harbor

• 09:00

  Departure by ferry ‘Brakzand’ to mainland

Posters, format A0, portrait

• Pseudo Action Potentials (PAPs) in red blood cells – an approach of understanding
  Lars Kaestner, University of Saarland, Germany

• Anemia in aged mice is accompanied by reduced erythroid lineage cell production and increased red blood cell life span
  Carsten Alt, Pfizer

• A novel allosteric activator of pyruvate kinase enhances human and mouse enzymatic activity and leads to hematological improvements in sickle cell disease mouse models
  Carsten Alt, Pfizer

• Can the emergence of cation channel activity during storage threaten the survival of transfused red blood cells?
  Stephane Egee, CNRS, France

• Cell Therapy Scale-up: Bioprocess Development for the Production of Hematopoietic Cells
  Brenda Juarez Garza, Delft University, the Netherlands

• The quality of red blood cells isolated from cord blood during storage
  Joyce Bestebroer, Sanquin, the Netherlands

• Variability of extracellular particle content in red blood cell concentrates upon storage is associated with differential membrane alterations and could be used as quality control
  Donatienne Tyteca, UC Louvain, Belgium

• Hemoglobin as a multifunctional sensor and buffer
  Anna Bogdanova, University of Zurich, Switzerland

• Scale-up of stem cell cultures from shake flask to bioreactor: a CFD-based comparison of hydrodynamic stress
  Ramon van Valderen, Delft University, the Netherlands

• Towards an improved erythroid production from IPSC
  Marien van der Stel, Sanquin, the Netherlands

• Investigating the Role of Shear Stress on Endothelial-to-Hematopoietic Transitioning
  Oyishee Ahmad, Sanquin, the Netherlands

• A clinical mechanical marker of red blood cell deformability: sickle cell disease example
  Cecile Jebane, CNRS-CINam, Marseille, France

• RBC delivered antigens for the induction of antigen specific immune tolerance,
  Youmna Al Halabi, Sanquin, the Netherlands

programma

Klik hier voor inschrijving

Woensdag 12 juni 2024

• 18:00 uur

  Verzamelen Lauwersoog

• 18:30 uur

  Vertrek boot naar Schiermonnikoog, aankomst 19.15 uur

• 20:00 uur

  Gezamenlijk diner

Donderdag 13 juni 2024

• 07:30 uur

  Ontbijt

• 08:25 uur

  Opening van de 4e nascholingscursus Casuïstiek in de nefrologie bij de volwassen populatie
  Iedere voordracht start met 30 minuten inleiding, waarna een uur casuïstiek behandeld wordt. De deelnemers worden uitgenodigd eigen casuïstiek in te brengen

• 08:30 uur

  HDF: is inmiddels iedereen convinced?
  Rob van Kruijsdijk, internist-nefroloog, Radboud UMC

• 10:00 uur

  Koffiepauze

• 10:30 uur

  Koorts bij een getransplanteerde patiënt, waar moet ik aan denken?
  Femke Molenaar , internist-nefroloog, UMC Utrecht

• 12:00 uur

  Lunchpauze

• 13:00 uur

  ANCA vasculitus 
  Hilde Remmelts, internist-nefroloog, Meander Medisch Centrum, Amersfoort

• 14:30 uur

  Theepauze

• 15:00 uur

  ‘Water en zout’ Interactieve presentatie over diagnostiek en behandeling van elektrolytproblemen. Een traktatie van water, zout en een klein beetje zuur. Ewout Hoorn, internist-nefroloog, Erasmus MC Rotterdam

• 16:30 uur

  Afsluiting

• 17:00 uur

  Einde programma dag 1

Vrijdag 14 juni 2024

• 07:30 uur

  Ontbijt en uitchecken

• 08:25 uur

  Opening dag 2 
  Iedere voordracht start met 30 minuten inleiding, waarna 45 minuten casuïstiek behandeld wordt

• 08:30 uur

  Familiaire cystenieren, waarom makkelijk als het ook moeilijk kan? Mahdi Salih, internist-nefroloog, Erasmus MC, Rotterdam

• 09:45 uur

  Koffiepauze

• 10:15 uur

  Intoxicaties in de nefrologie. Wanneer wat te doen? 
  Douwe Dekker, internist-acuut geneeskundige, UMC Utrecht

• 11:30 uur

  Membraneuze glomerulopathie 
  Anne-Els van de Logt , internist-nefroloog, Radboud UMC

• 12:45 uur

  Lunchpauze

• 13:45 uur

  Complement gemedieerde nierziekten: een Crash Course
  Caroline Duineveld, internist-nefroloog, Radboud UMC

• 15:00 uur

  Einde nascholingscursus

• 15:45 uur

  Vertrek met bus naar haven Schiermonnikoog

• 16:30 uur

  Vertrek boot naar Lauwersoog

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