10 Congress of the French Society of Cell and Gene Therapy
Transcription
10 Congress of the French Society of Cell and Gene Therapy
10th Congress of the French Society of Cell and Gene Therapy Nantes, 6-8 June 2011 MONDAY 6 JUNE 10:30 –12:45 Vectors and tools “10 years on” Chairpersons: François-Loïc Cosset et Karim Benihoud Hildegard Büning, Department I of Internal Medicine and Center for Inv1 Molecular Medicine Cologne (ZMMK), University of Cologne, Germany Tailoring adeno-associated viral vectors for gene transfer and gene therapy Andrew Baker, Department of Molecular Medicine, University of Inv2 Glasgow, United Kingdom Adenovirus tropism: mechanisms and exploitation François-Loïc Cosset , 1INSERM U758, Ecole Normale Supérieure de Inv3 Lyon, France Stealth lentiviral vectors targeted to hematopoietic cells Selected Abstracts Madeleine Zerbato, Genethon, Evry, France Genomic targeting with group II introns: characterization of Pl.LSU/2 intron protein and evidence for intron splicing activity Mattias Lindberg, INSERM U613, Université de Bretagne Or1 Or2 Occidentale, Brest, France Gene therapy of cystic fibrosis : plasmid DNA contribution on in vivo lipid-based transfection efficacy Vanessa Gauttier, INSERM UMR948 , Nantes, France Evaluation of the tumorigenic potential of AAV transduction in the newborn rat liver 12:45–14:00 Lunch 14:00 –16:15 Imaging and Gene Transfer Chairpersons: G. Vassaux et Patrick Midoux Georges Vassaux, Inserm U948, CHU Hotel Dieu, Nantes, France Molecular imaging of genes expression using the Na/I, symporter: applications in gene therapy Andy Miller, Institute of Pharmaceutical Science,University College, Or3 Inv4 Inv5 London, UK Delivering on RNAi Therapeutics, Molecular Imaging and Theranostics; what do we think that we know? Veerle Baekelandt, Division of Molecular Medicine, University of Inv6 Leuven, Belgium In vivo gene transfer and non-invasive imaging in rodent brain with viral vectors: progress and challenges 1 06/04/2011 10th Congress of the French Society of Cell and Gene Therapy Nantes, 6-8 June 2011 Selected Abstracts Yuan Ping, Supramolecular Biomaterials Laboratory, National Or4 Univeristy of Singapore, Republic of Singapore PEG-detachable cationic polymer for FGFR-targeted delivery of p53 Thomas Bucher, INSERM UMR649, Nantes, France New AAV-based strategies for gene therapy of a feline SMA model Thi My Anh Neildez, Généthon, Evry, France Physiologic oxygen levels improve in-vitro generation of regulatory T Lymphocytes. 16:15 –16:45 Break 16:45 –18:45 Biotech Forum Or5 Or6 Chairpersons: Sophie Gomez et Sophie Lebel-Binay Introduction by Atlanpole Biotherapies - Olivier Boisteau, Clean Cells Local Companies Testimonies: In Cell Art, Bruno Pitard/Chloé Bellocq Affilogic, Olivier Kitten TcL Pharma, Maryvonne Hiance From Research to the Production of Therapies : -A new approach to Cell Therapy for the Heart, results of Bonami trials – Patricia Lemarchand -A production tool for Cells, the UTCG - Sylvain Bercegeay Development of Cell and Gene Therapies: Issues and perspectives Progress update « Cell therapy manufacturing: stem cells and immunobiotherapies » – Christophe Iochem, Clean Cells Presentation of the European Project TERM – Agnès Kammoun 18:45 –19:30 Opening Lecture Thierry VandenDriessche, Free University of Brussels (VUB), Brussels, Belgium. Cell and Gene Therapy, 10 years on. 19:45 –21:00 Welcome Reception (co-sponsored by Atlanpole Biotherapie) Brasserie Felix TUESDAY 7 JUNE 9:00 -10:45 Cell therapy and transplantation Chairpersons: Gilles Blancho et Michel Pucéat Gilles Blancho, INSERM UMR 643, CHU de Nantes, France Use of transgenic and cloned animals in xenotransplantation José V. Castell, Dep.de Bioquímica, Hospital Universitario La Fe, Valencia, Spain HEPATIC CELL THERAPY: WHEN?, WITH WHICH CELLS?, WHICH CLINICAL OUTCOME?. (THE EXPERIENCE OF VALENCIA). Inv7 Inv8 2 06/04/2011 10th Congress of the French Society of Cell and Gene Therapy Nantes, 6-8 June 2011 Selected Abstracts Elodie Fourquet, INSERM U1037 Toulouse, France Using engineered stromal cells for the targeted therapy of liver carinoma Wenwei Zhang, Inserm U972, Kremlin-Bicêtre, France Characterization at the clonal level of mesenchymal stem cells from human fetal liver Nicolas Petit, INSERM U95, Hôpital de la Pitié Salpêtrière, Paris, Or7 Or8 Or9 France Progress towards gene therapy of HIV infection in humanized mice 10:45 -11:15 Break 11:15 -12:45 Muscular and neuromuscular therapies Chairpersons: Luis Garcia et Anna Salvetti Karl Rouger, UMR 703 INRA, Ecole Nationale Vétérinaire, Nantes Inv9 Atlantique, France Long-term muscle repair and clinical efficacy in Duchenne Muscular Dystrophy dogs after systemic delivery of allogenic Muscle Stem (MuStem) cells Luis Garcia, Biothéraphies des maladies du système neuromusculaire, Inv10 UMRS 974/Institut de myologie, Paris, France Antisense delivery for mRNA-based therapeutics for neuromuscular diseases. Selected Abstracts Alberto Epstein, CGphiMC - UMR5534 CNRS - Université Lyon 1, Or10 France Silencing of NMDA receptor NR1 subunit using HSV-1-derived amplicon vectors impairs cognitive functions in rats and reduces amyloid-beta oligomers binding and toxicity in cultured neurons. Caroline Sevin , INSERM U745, Paris, France Brain gene therapy for Metachromatic Leukodystrophy using AAVrh10 vector : optimized clinical protocol 12:45 -14:30 Lunch Sponsored by THERMOFISHER Thermo Prize Awards Ceremony 14:30 -15:15 SFTCG ASSEMBLEE GENERALE DES MEMBRES Or11 3 06/04/2011 10th Congress of the French Society of Cell and Gene Therapy Nantes, 6-8 June 2011 15:15 -17:30 Vectors and immune response Chairpersons: François Lemoine et Anne Galy Bernhard Ryffel, Labo d'immunologie et embryologie moléculaire, Inv11 UMR 6218 CNRS, Université d'Orléans, France Innate immune response: Mechanisms and pathways Anne Galy, Genethon, Evry, France Mechanisms of immunization by gene transfer Jennifer Richardson, UMR 1161 Virologie Inra, Anses, ENVA, Inv12 Inv13 Maisons-Alfort, France Antigen encoded by vaccine vectors derived from human adenovirus serotype 5 is preferentially presented to CD8+ T lymphocytes by the CD8alpha+ dendritic cell subset Selected Abstracts Aurelie Ploquin, INSERM U758, ENS Lyon, France Recombinant AAV vectors as genetic vaccines to induce a neutralising humoral response against nipah virus Geraldine Lescaille, UPMC Paris 06 & UMR CNRS 7211/INSERM Or12 Or13 U959,Paris, France Vaccine strategy based on DNA vaccines forming E7 recombinant retrovirus-like particles for the treatment of HPV-induced head and neck cancers Christine Chauveau, INSERM U649, Nantes, France Impact of the immune system on rAAV2/4.hRPE65 mediated gene delivery in retina: Efficacy of sequential subretinal readministration of rAAV2/4.hRPE65 in RPE65-/- dogs. 17:30 -19:00 POSTERS 19:30 -22:00 Gala Dinner (Invitations or Pre-booking only) Or14 MERCREDI 8 JUIN 8:30-10:45 Innovative cell and gene therapies in cancer Chairpersons: Daniel Scherman et Pierre Cordelier Inv14 Daniel Scherman, Laboratory of Chemical and Genetic Pharmacology Inv15 and of Imaging - UMR 8151 CNRS - U1022 Inserm - Paris Recent progress in non viral gene delivery and therapy Jean Rommelaere, DKFZ Dept. F010 and INSERM Unit 701, Inv16 Deutsches Krebsforschungszentrum, Heidelberg, Germany Virotherapy of glioblastoma 4 06/04/2011 10th Congress of the French Society of Cell and Gene Therapy Nantes, 6-8 June 2011 Selected Abstracts Joe-Marc Chauvin, INSERM U892 F-44093, Nantes, France The cross-priming of tumor reactive cytotoxic T cells by synthetic long peptides depends on a sufficient HLA binding of the CD8 epitope. Valerie Trichet, INSERM UMR957 Faculté de médecine, Nantes, Or15 Or16 France Therapeutic interest of RNA interference molecules in two rare bone diseases Flavie Sicard, INSERM UMR1037, Toulouse, France In vivo targeting of microRNA 21 using lentiviral vectors for the gene therapy of pancreatic cancer 10:45-11:15 Break 11:15-13:00 POSTERS 13:00-14:00 LUNCH 14:00-16:30 Clinical trials « 10 years on » Chairpersons: Odile Cohen Hagenhauer et Nathalie Cartier Salima Hacein-Bey, Département de biothérapies, Hôpital Necker Or17 Inv17 Enfants-Malades, Paris, France Ten years of gene therapy for SCID-X1 Amit Nathwani, Departmentof Haematology, University College Inv18 London ,KD Haemophilia Centre and Thrombosis Unit, Royal Free NHS Trust, NHS Blood and Transplant, U.K A phase I/II clinical trial entailing peripheral vein administration of a novel self complementary adeno-associated viral vector encoding human FIX for haemophilia B gene therapy Graziella Pellegrini, Centre for Regenerative Medicine "Stefano Inv19 Ferrari", Modena, Italy Limbal stem-cell therapy and long-term corneal regeneration Selected Abstracts Marie-Anne Burlot, U745 INSERM, Faculté de Pharmacie, Paris, Or18 France Evaluation of cholesterol 24S-hydroxylase overexpression by AAV-gene transfer as a potential therapeutic target for Alzheimer’s Disease-Like Tau Neuropathology Caroline Le Guiner, GENETHON, Evry, France Effective limb transduction and phenotypic correction after injection of rAAV8-U7snRNA in GRMD dogs Or19 Closing David Klatzmann, UPMC CNRS UMR 7211 / INSERM U959,Groupe Hospitalier Pitié Salpêtrière, Paris, France 5 06/04/2011