Raffaele Renella
Raffaele Renella | |
|---|---|
| Education | Medicine (MD) MD-PhD |
| Alma mater | University of Geneva University of Oxford |
| Known for | Research on bone marrow failure Congenital dyserythropoietic anemia Gene therapy for hemoglobinopathies |
| Awards | Lord Florey Scholarship (2005) |
| Scientific career | |
| Fields | Pediatric hematology and oncology Hematopoiesis Gene therapy |
| Institutions | Lausanne University Hospital (CHUV) University of Lausanne (UNIL) Boston Children's Hospital Dana-Farber Cancer Institute |
| Thesis | (2009) |
| Doctoral advisor | William G. Wood Douglas R. Higgs |
| Other academic advisors | Alain Fischer David A. Williams |
Raffaele Renella is a Swiss pediatric hematologist and oncologist. He is an Associate Professor at the University of Lausanne (UNIL) and the Head of the Pediatric Hematology-Oncology Unit at the Lausanne University Hospital (CHUV).[1] His research focuses on anomalies of hematopoietic stem cell differentiation, bone marrow failure, and the development of gene and cell therapies for inherited blood disorders.[2] In 2026, he was appointed as the vice-director of the Swiss NCCR "Children & Cancer" funded by the SNSF.[3]
Career
Renella obtained his Medical Degree (MD) from the University of Geneva. He completed his residency in pediatrics at the Lausanne University Hospital (CHUV).[2] In 2004, he undertook specialized training in pediatric hematology, immunology, and stem cell transplantation at the Hôpital Necker-Enfants Malades in Paris, working in the unit led by Alain Fischer.[4]
From 2005 to 2009, Renella pursued a PhD with William G. Wood and Douglas R. Higgs in Molecular Hematology at the University of Oxford (Weatherall Institute of Molecular Medicine). As a Lord Florey Scholar, he conducted research on congenital dyserythropoietic anemia.[5] During this period, he also served as an Honorary Specialist Registrar at the John Radcliffe Hospital.[6]
In 2010, Renella relocated to the United States for a fellowship in Pediatric Hematology-Oncology and Stem Cell Transplantation at Boston Children's Hospital, the Dana-Farber Cancer Institute, and Harvard Medical School.[7] He conducted postdoctoral research in the laboratory of David A. Williams.[8] From 2013 to 2014, he served as an Instructor of Pediatrics at Harvard Medical School and an Attending Staff Physician at Boston Children's Hospital and Dana-Farber.[9]
Renella returned to Switzerland in 2015, assuming the role of Attending Physician-Consultant (Médecin-associé) and Head of the Pediatric Hematology-Oncology Research Laboratory (LHOP) at CHUV.[2] In August 2023, he was appointed Head of the Pediatric Hematology-Oncology Unit (Chef de service) at CHUV. Concurrently, he serves as the Pediatric Hematology Group Leader at the LHOP.[10] He holds board certifications from the Swiss Medical Association (FMH) in Pediatrics and Pediatric Hematology-Oncology, and is a Fellow of the Royal College of Paediatrics and Child Health (FRCPCH).[2]
In 2026, he was appointed as vice-director in the newly created National Centre of Competence in Research (NCCR) "Children & Cancer" project funded by the SNSF with a total funding of almost CHF 34 million over four years.[3]
Research
Renella leads a research group affiliated with the University of Lausanne and the Swiss Cancer Center Léman (SCCL).[11] His work investigates the molecular mechanisms underlying hematopoietic stem cell anomalies, with a focus on bone marrow failure, myelodysplastic syndromes,[12] and hemoglobinopathies such as sickle cell disease.[13] His laboratory is involved in translational research aimed at developing gene and cell therapy approaches, including hematopoietic stem cell transplantation and CAR-T cell immunotherapies.[14][15] Renella has contributed to research on lineage-specific BCL11A knockdown strategies to reverse the sickle phenotype and has studied the genetic basis of congenital dyserythropoietic anemias.[16] He also participates in the development of clinical guidelines, such as consensus recommendations for managing iron deficiency in children.[17] He is a member of the Swiss Pediatric Oncology Group (SPOG)[18] and the European Hematology Association.[19] He serves on the Medical & Scientific Advisory Board at the European Sickle Cell Federation.[20]
Distinctions
- Fellow of the Royal College of Paediatrics and Child Health (FRCPCH)[2]
- 2012: ASH Outstanding Abstract Achievement Awards[21]
- 2005: Lord Florey Scholarship (Berrow Foundation), University of Oxford[20]
Selected works
- Renella, R.; et al. (2020). "Diagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group". European Journal of Pediatrics. 179 (10): 1637–1646. doi:10.1007/s00431-020-03597-5.
- Brendel, C.; Renella, R.; et al. (2016). "Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype". Journal of Clinical Investigation. 126 (10): 3868–3878. doi:10.1172/JCI87323.
- Renella, R.; et al. (2011). "Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1alpha localization in erythroblasts". Blood. 117 (25): 6928–6935. doi:10.1182/blood-2010-11-316661.
- Groschel, S.; Renella, R.; et al. (2023). "Highly connected 3D chromatin networks established by an oncogenic fusion protein shape tumor cell identity". Science Advances. 9 (15): eabq7232. doi:10.1126/sciadv.abq7232.
{{cite journal}}: CS1 maint: article number as page number (link) - Renella, R.; et al. (2014). "Genetic deletion of the GATA1-regulated protein Alpha-Synuclein reduces oxidative stress and nitric oxide synthase levels in mature erythrocytes". American Journal of Hematology. 89 (7): 725–731. doi:10.1002/ajh.23722.
References
- ^ "Pediatric Hematology-Oncology Research Laboratory". UNIL. Retrieved 2026-02-13.
{{cite web}}: CS1 maint: url-status (link) - ^ a b c d e "Pr Raffaele Renella". CHUV (in French). Retrieved 2026-02-13.
- ^ a b Swiss State Secretariat of Education, Research and Innovation SERI. "National Centre of Competence in Research "Children & Cancer"" (PDF). SBFI. Retrieved 2026-02-12.
- ^ Renella, Raffaele; Picard, Capucine; Neven, Bénédicte; Ouachée‐Chardin, Marie; Casanova, Jean‐Laurent; Deist, Françoise Le; Cavazzana‐Calvo, Marina; Blanche, Stéphane; Fischer, Alain (2006-09-01). "Human leucocyte antigen‐identical haematopoietic stem cell transplantation in major histocompatiblity complex class II immunodeficiency: reduced survival correlates with an increased incidence of acute graft‐ versus ‐host disease and pre‐existing viral infections". British Journal of Haematology. 134 (5): 510–516. doi:10.1111/j.1365-2141.2006.06213.x. ISSN 0007-1048.
- ^ Renella, Raffaele; Roberts, Nigel; Brown, Jill M; De Gobbi, Marco; Bird, Louise; Hassanali, Tasneem; Sloane-Stanley, Jacqueline; Sharpe, Jacqueline A; Cordell, Jacqueline Loelia; Ferguson, David J.P.; Buckle, Veronica; Higgs, Douglas R.; Wood, William G (2010-11-19). "Codanin-1 Mutations In Congenital Dyserythropoietic Anemia Type 1 Affect HP1α Localization In Erythroblasts". Blood. 116 (21): 1003–1003. doi:10.1182/blood.V116.21.1003.1003. ISSN 0006-4971.
- ^ Renella, Raffaele; Wood, William G. (2009-04-01). "The Congenital Dyserythropoietic Anemias". Hematology/Oncology Clinics of North America. 23 (2): 283–306. doi:10.1016/j.hoc.2009.01.010.
- ^ "Potential gene therapy approach to sickle cell disease highlighted at national hematology meeting". www.dana-farber.org. Retrieved 2026-02-13.
- ^ Renella, Raffaele; Schlehe, Julia S.; Selkoe, Dennis J.; Williams, David A.; LaVoie, Matthew J. (2014-10-01). "Genetic deletion of the GATA1‐regulated protein α‐synuclein reduces oxidative stress and nitric oxide synthase levels in mature erythrocytes". American Journal of Hematology. 89 (10): 974–977. doi:10.1002/ajh.23796. ISSN 0361-8609.
- ^ Marchese, Halle (2022-04-27). "A mystery launched a decade-long quest, leading to a novel cause of bone marrow failure". Institute for Protein Innovation. Retrieved 2026-02-13.
- ^ "Laboratoire de recherche en hématologie-oncologie pédiatrique (LHOP) du CHUV". CHUV (in French). Retrieved 2026-02-13.
- ^ "Raffaele Renella Associate Professor - Pediatry - (UNIL)". applicationspub.unil.ch. Retrieved 2026-02-13.
- ^ Renella, Raffaele; Gagne, Katelyn; Beauchamp, Ellen; Schlaeger, Thorsten; Hofmann, Inga; Shimamura, Akiko; Fogel, Jonathan; Agarwal, Suneet; Ebert, Benjamin L.; Markianos, Kyriacos; Springer, Timothy A.; Fleming, Mark D.; Williams, David A. (2018-11-29). "Congenital X-Linked Myelodysplasia with Tetraploidy Is Associated with De Novo Germline C-Terminal Mutation of SEPT6, a Septin Filament Protein". Blood. 132 (Supplement 1): 644–644. doi:10.1182/blood-2018-99-114682. ISSN 0006-4971.
- ^ Renella, Raffaele (2021-09-01). "Biomarkers for the central nervous system complications of sickle cell disease: are we there yet?". PROTEOMICS – Clinical Applications. 15 (5). doi:10.1002/prca.202100026. ISSN 1862-8346.
- ^ De Vita, Serena; Harris, Chad E; Renella, Raffaele; Mathieu, Ronald; McGuinness, Meaghan; Williams, David A. (2012-11-16). "Vav1 Deficiency Differentially Affects Engraftment of Fetal Hematopoietic Organs During Development Compared with Adult Marrow After Transplantation". Blood. 120 (21): 1212–1212. doi:10.1182/blood.V120.21.1212.1212. ISSN 0006-4971.
- ^ "Science". AAAS. doi:10.1126/sciadv.adu5754. PMC 12204177. PMID 40577481. Retrieved 2026-02-13.
- ^ Brendel, Christian; Guda, Swaroopa; Renella, Raffaele; Bauer, Daniel E.; Canver, Matthew C.; Kim, Young-Jo; Heeney, Matthew M.; Klatt, Denise; Fogel, Jonathan; Milsom, Michael D.; Orkin, Stuart H.; Gregory, Richard I.; Williams, David A. (2016-10-03). "Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype". The Journal of Clinical Investigation. 126 (10): 3868–3878. doi:10.1172/JCI87885. ISSN 0021-9738.
- ^ Mattiello, Veneranda; Schmugge, Markus; Hengartner, Heinz; von der Weid, Nicolas; Renella, Raffaele; on behalf of the SPOG Pediatric Hematology Working Group (2020-04-01). "Diagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group". European Journal of Pediatrics. 179 (4): 527–545. doi:10.1007/s00431-020-03597-5. ISSN 1432-1076.
- ^ "Jahresbericht 2020" (PDF). SPOG. Retrieved 2026-02-13.
- ^ "Chairs and members". The European Hematology Association (EHA). Retrieved 2026-02-13.
- ^ a b "Medical & Scientific Advisory Board". escfederation.eu. Archived from the original on 2025-12-10. Retrieved 2026-02-13.
- ^ "Outstanding Abstract Achievement Awards". www.hematology.org. Retrieved 2026-02-13.