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Inscription statutaire congrès 2010
Inscription non statutaire congrès 2010
Inscription industriel congrès 2010
| SUNDAY JUNE 13 | |
| 13h45 | Opening ceremony Chairpersons : Nathalie Cartier and François Lemoine |
| 14h00- 14h45 | Special lecture : Thierry HEIDMANN (UMR-8122, IGR, France) Endogenous retroviruses and the placental "syncytins": natural history of reiterated and successful retroviral gene transfers in the course of mammal evolution |
| 14h45- 16h45 | Gene therapy for the central nervous system Chairpersons: David Klatzmann and Alberto Epstein
Brain gene therapy for metachromatic leucodystrophy: towards clinical trial.
Targeted gene-based strategies for control of spinal cord glial signaling pathways : impact on local neuroinflammation and pathological pain. |
| 16h45- 17h15 |
Coffee break |
| 17h15- 19h15 | David FINK (Dpt of Neurology, University of Michigan, USA)
A phase I clinical trial of gene transfer for the treatment of intractable pain Patrick AUBOURG (UMR-745, Hôpital St Vincent de Paul, Paris)
Prevention of the development of glycogen storage disease in a mouse model of liver-specific deletion of glucose-6 phosphatase, by in vivo lentiviral gene therapy
Optimization of Integration-Defective Lentiviral Vectors production and sustained production of erythropoietin after lentiviral administration to the liver
Muscle-specific expression of myotubularin corrects the phenotype of targeted muscles in mouse models of X-linked myotubular myopathy |
| 19h15-21h00 |
Poster session (viewing) & welcome reception |
| MONDAY JUNE 14 | |
| 8h30-10h45 |
Non-viral Gene Therapy Session Functional dissection of mosquito immune responses by RNAi - opportunities and limitations Gilles DIVITA (UMR-5237, Centre de Recherches de Biochimie Macromoléculaire, Montpellier) Peptide-based nanoparticles for in vivo delivery of siRNA Virginie ESCRIOU (UMR-8151, Inserm U1022, Fac pharma, Paris) Efficient lipoplexes for administration of siRNA Selected oral presentations
Modulation of gene expression in the lung using ARN interference
Targeting oncogenic microRNAs using lentiviral vectors for the gene therapy of pancreatic cancer.
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| 10h45-11h15 | Coffee Break |
| 11h15-13h00 |
Vaccinology – Immunotherapy – Infectious diseases Powerful cellular immunity to two sand fly salivary proteins in dogs: could this set the stage for a superior anti-Leishmania vaccine? Wei- Zen WEI (Wayne State University, Detroit, MI, USA) DNA vaccines in cancer therapy Selected oral presentations
Control of the anti-transgene immune responses with miRNA142.3p-regulated rAAV2/1 vectors is not as efficient in dystrophic as in normal mice
Pre-existing anti-adenovirus immune responses control the efficacy of vaccines based on epitope display on adenovirus capsid
Regulatory pro-B cell progenitors for cell therapy of type 1 diabetes |
| 13h00- 15h00 | LUNCH |
|
POSTER SESSION I |
|
| 15h00-16h00 |
General Assembly of SFTCG |
| 16h00-18h30 | Cell Therapy Session CD4+CD25+ regulatory T-cell depletion improves the graft-versus-tumor effect of donor lymphocytes after allogeneic hematopoietic stem cell transplantation François PATTOU (U857, CHR de Lille) Cell therapy for diabetEs: Where ? Human embryonic stem-cell derivatives for full reconstruction of the pluristratified epidermis: a preclinical study
Following telomeres after cell reprogramming and differentiation of iPS cells
Modelling Familial Hypercholesterolemia by hepatic differentiation of patient specific hiPS cells.
Intramuscular transplantation of human postnatal myoblasts in immunodeficient mice produces functional graft-derived satellite cells. |
| TUESDAY JUNE 15 | |
| Special thematic session: “Targeted integration, epigenetic and chromatin regulation” | |
| 8h30-10h15 | Homologous Recombination Meganucleases and gene therapy: different strategies
The Rous Sarcoma Virus promoter carried by a rAAV vector is resistant to DNA methylation in primate muscle and liver
Stochastic epigenetic fluctuations of transgene expression
Epigenetic changes induced in human hematopoietic progenitor/stem cells following ex vivo lentiviral transduction |
| 10h15-10h45 | Coffee Break |
| 10h45-11h45 |
Homologous Recombination: applications Combining Site-Specific Integration and Cassette Design to Achieve Robust Expression without Impacting Endogenous Gene Expression Ignacio ANEGON (UMR-643, Nantes, France) Zinc-finger nucleases: a powerful tool for genetic engineering of animals |
| 11h45-13h00 | POSTER SESSION II |
| 13h00-14h00 | LUNCH |
| 14h00-15h30 |
Epigenetics, chromatin and nuclear organization Gene regulation: from chromatin structure to nuclear compartmentalization Chromatin marks and subnuclear positioning at lineage-affiliated genetic programs to predict differentiation potential of multipotent hematopoietic progenitors Manuel GREZ (Institute for Biomedical Research, Frankfurt, Germany) A lentiviral vector for the correction of Chronic Granulomatous Disease containing a chromatin opening element provides copy-dependent expression and resistance to CpG methylation. |
| 15h30-16h00 | Best oral presentation and best poster awards |
| Closure | |