iNFLAMMATION iMMUNOPATHOLOGY BIOTHERAPY
Transcription
iNFLAMMATION iMMUNOPATHOLOGY BIOTHERAPY
iNFLAMMATION iMMUNOPATHOLOGY BIOTHERAPY U N I V E R S I T Y H O S P I TA L D E PA RT M E N T - D H U The i2B Department has 32 médical and research teams working together to improve the management of inflammatory and autoimmune diseases. C O O R D I N AT O R S : P r o f . S e r g e A m s e l e m & P r o f . D a v i d K l a t z m a n n T E N O N - S A I N T-A N TO I N E - A R M A N D -T R O U S S E AU - P I T I É-S A L P Ê T R I È R E - I N R A J O U Y- E N -J O S A S CONTEXT C hronic inflammation, a condition present in various diseases including those with an immune component, is an important cause of morbidity/ mortality in the developed world. Recent advances on the pathophysiology of autoinflammatory/autoimmune diseases have led to a re-examination of their nosology. It now appears that autoinflammatory and autoimmune diseases do not represent two distinct categories of disorders. Rather, they form a disease continuum ranging from pure autoinflammatory disorders to pure autoimmune diseases, encompassing a large panel of inflammatory diseases with some autoimmune component, and vice versa. A wide range of disorders fall into this disease category. These are rare or common disorders, whose management requires an integrated approach in which clinicians from internal medicine or medical specialities and research teams collaborate closely in translational research programs. RATIONALE OBJECTIVE The rationale of i2B is based on : Our general objective is to study and improve management of inflammatory and autoimmune diseases by integrating translational information. • The concept of autoinflammatory/autoimmune disease continuum (AADC) • The expected benefits of managing rare disorders together with common diseases • The importance of transition from pediatric to adult healthcare departments i2B disease CONTINUUM AUTOINFLAMMATION RARE MONOGENIC AUTOINFLAMMATORY DISEASES POLYGENIC AUTOINFLAMMATORY DISEASES MIXED PATTERN DISEASES CLASSIC POLYGENIC AUTOIMMUNE DISEASES (ORGAN SPECIFIC AND NONSPECIFIC) RARE MONOGENIC AUTOIMMUNE DISEASES FMF, TRAPS, HIDS, CAPS, PAPA Blau Syndrome Crohn’s disease, ulcerative colitis Degenerative diseases, e.g.osteoarthritis Gout/pseudogout/other crystal arthropathies Some categories of reactive arthritis and psoriasis/psoriatic arthritis Congenital diseases with associated tissue inflammation Non-antibody associated vasculitis including giant cell and Takayasu arteritis Idiopathic uveitis Erythma nodosum associated disease, including sarcoidosis Ankylosing spondylitis Reactive arthritis; psoriasis/psoriatic arthritis Behcet’s syndrome Uveitis (HLA-B27 associated) Rheumatoid arthritis Autoimmune uveitis (sympathetic ophthalmia) Myasthenia gravis Dermatomyositis, scleroderma Goodpasture syndrome ANCA-associated vasculitis Type 1 diabetes Sjogren’s syndrome Systemic lupus erythematosus Membranous nephropathy ALPS IPEX Adapted from D. Mc Gonagle & M. McDermott PLoS Medicine August 2006 AUTOIMMUNITY ALPS: Autoimmune Lymphoproliferative Syndrome, ANCA: Antineutrophil Cytoplasmic Antibodies, CAPS: Cryopyrin-Associated Periodic Syndrome; IPEX: Immune dysregulation, Polyendocrinopathy, Enteropathy, X-linked, FMF: Familial Mediterranean Fever, HIDS: Hyperimmunoglobulinemia D with periodic fever syndrome, HLA: Human Leukocyte Antigen, PAPA: Pyogenic Arthritis, Pyoderma gangrenosum, and severe cystic Acne, TRAPS: Tumour Necrosis Factor Receptor– Associated Periodic fever Syndrome. STRATEGY I2B is a collegial network to strengthen the links between patient care, research, and teaching in the field of autoimmune/autoinflammatory diseases. For this purpose, i2B projects are structured in four complementary workpackages. © INSERM/ Patrice Latron 1 Patient Care, Cohorts, Deep phenotyping & Clinical trials © INSERM/ Patrick Delapierre 2 Basic and translational research Cross-analyse phenomic data from cohorts of patients with selected inflammatory and autoimmune diseases. Identify new/common molecular pathways in several diseases and validate pronostic and diagnostic biomarkers. © INSERM/ François Guenet 3 Translational medicine and biotherapy © INSERM/ Etienne Begouen 4 Teaching and dissemination EXPECTED IMPACT Develop and evaluate biotherapies and novel therapeutic targets. Implement high-level teaching and training activities for healthcare professionals and patients. We aim to improve the classification, diagnosis, treatment and management of autoimmune/ autoinflammatory diseases so as to offer a better quality of life to patients. High-level teaching and dissemination activities will spread knowledge and expertise in this cutting-edge field of medical science. i2B TEAMS Clinical Teams Team Leader Department Hospital F. Berenbaum Rheumatology Saint-Antoine L. Baud Department of Physiology Tenon J. Cabane Internal Medecine Saint-Antoine P. Cacoub Internal Medecine 2 Pitié-Salpêtrière J. Cadranel Department of Pneumology and Intensive Care Medecine Tenon A. Clement Pediatric Pneumology Trousseau J. Cosnes Gastroenterology and Nutrition Saint-Antoine B. Fautrel Rheumatology Pitié-Salpêtrière G. Grateau Internal Medecine Tenon P. Le Hoang Ophthalmology Pitié-Salpêtrière S. Herson Internal Medecine 1 and Integrated Gene Therapy Center Pitié-Salpêtrière M. Mayer Neuropediatrics Trousseau P. Ronco Nephrology and Dialysis Tenon E. Rondeau Intensive care nephrology and Transplantation department Tenon T. Ulinski Pediatric Nephrology Trousseau Clinical laboratory teams Team Leader Department Hospital S. Amselem Molecular Genetics Unit Trousseau I. Brocheriou Department of Pathology Tenon J. Capeau Department of Biochemistry Tenon D. Klatzmann Clinical Investigation Center for Biotherapies (CIC-BTi) Pitié-Salpêtrière D. Klatzmann Biotherapy Unit Pitié-Salpêtrière G. Trugnan Platform for Peptidomic, Metabolomic and drug Measurements (Mass Spectrometry) Saint-Antoine Unit Hospital Research teams Team Leader S. Amselem P. Aucouturier O. Benveniste Pathophysiology of Pediatric Genetic Diseases / UMRS 933 INSERM/ UPMC Neuroimmunology / UMRS 938 INSERM / UPMC Inflamed muscle and Innovative Targeted Therapies / U974 / UM76, INSERM / UPMC Trousseau Saint-Antoine Pitié-Salpêtrière F. Berenbaum Metabolism and age-related joint diseases / UMRS 938/INSERM / UPMC Saint-Antoine C. Chatziantoniou From Kidney Phenotypic Alterations to Novel Diagnostic Markers and Targets of Therapy of CKD / UMRS1155 INSERM / UPMC Tenon A. Clément Pediatric Pneumology / UMRS 938 INSERM / UPMC Trousseau D. Klatzmann P. Langella P. Ronco P. Seksik A. Six Immunology-Immunopathology-Immunotherapy / UMR 7211 - UMRS 959 UPMC / INSERM / CNRS Commensal and Probiotics-Host Interactions Laboratory / UMR1319 Micalis INRA From rare to common kidney diseases, remodeling and repair / UMRS1155 INSERM / UPMC Micro-organisms and Intestinal Physiopathology / ERL INSERM U1157 / UMR7203 UPMC / INSERM / CNRS / ENS Immunology-Immunopathology-Immunotherapy / UMR 7211 - UMRS 959 UPMC / INSERM / CNRS Pitié-Salpêtrière INRA Tenon Saint-Antoine Pitié-Salpêtrière i2B CONSORTIUM Multidisciplinary and complementary teams of excellence Within i2B, 21 medical teams and 11 research teams share and provide expertise in biological and clinical aspects of inflammation, immunology, genetics, microbiota and biotherapies. These teams are located in four university hospitals, (Pitié-Salpêtrière, Trousseau, Tenon and SaintAntoine) linked to Pierre and Marie Curie University (UPMC), and one team is located at the Institut National de la Recherche Agronomique (INRA). The complementary expertise of i2B teams covers the entire spectrum of the autoimmune/ autoinflammatory diseases. I2B has exclusive clinical resources comprising more than 25 cohorts and one Clinical Investigation Center specialized in biotherapies (CIC-BT). In addition, i2B collaborates closely with 5 National Reference Centers for Rare Diseases, the laboratory of excellence Transimmunom and 14 patient groups. 15 Clinical Teams (adult and pediatric) 6 Clinical Laboratory Research Teams Internal medecine, rheumatology, gastroenterology, nephrology, ophthalmology, pneumology, neurology > 25 cohorts Labex Transimmunom 3 academic laboratories and 3 biotech companies (INSERM, CNRS, INRA, UPMC) H O S P I TA L U N I V E R S I T Y D E PA•RT MENT - DHU Autoimmune/Inflammatory Pitié–Salpêtrière, Saint-Antoine, Tenon and Trousseau hospitals 1 Research Teams iNFLAMMATION 5 iMMUNOPATHOLOGY National Reference BIOTHERAPY Centers for Rare Diseases 1 Clinical Investigation Center in Biotherapy 11 Systemic Rare Diseases • Pediatric Lung Diseases • Secondary Amyloidosis and Familial Mediterranean Fever • Rare Hereditary Renal Diseases • Neuromuscular Diseases 14 Patient groups ANDAR, AFPric, AFA, AFLAR, AFS, AFFMF, Association contre l’amylose, AFM, Respirer C’est Grandir, FNAIR, AIRG, Fondation du Rein, RENIF, VLM ANDAR : Association Nationale de Défense Contre l’Arthrite Rhumatoide, AFPric : Association Française des Polyarthritiques, AFLAR, AFS : Association Française des Spondylarthritiques, AFM : Association Française Contre les Myopathies, AFFMF : Association Française de la Fièvre Méditéranéenne Familiale, FNAIR : Fédération Nationale Des Insuffisants Rénaux, RENIF : Réseaux de Néphrologie d’Ile de France, AFA : Association François Aupetit; VLM : Vaincre la Mucoviscidose. CO O RD INATOR S Prof. Serge Amselem Hôpital Armand Trousseau Service de génétique 26 avenue du Dr Arnold Netter 75012 Paris Prof. David Klatzmann Hôpital Pitié-Salpêtrière CIC Biothérapie 47-83 boulevard de l’hôpital 75013 Paris [email protected] Tél. 01 44 73 52 95 [email protected] Tél. 01 42 17 74 61 PARIS Tenon Saint-Antoine Armand-Trousseau Pitié-Salpêtrière INRA Jouy en Josas PA R T NE R S CON TACT Dr Caroline Aheng - Project Manager Mail : caroline. [email protected] Tél. : 01 42 17 74 67 iNFLAMMATION iMMUNOPATHOLOGY BIOTHERAPY U N I V E R S I T Y H O S P I TA L D E PA RT M E N T - D H U http://www.dhu-i2b.fr Création : i-breed.com Crédits photo © INSERM/ Banque Serimidis PU BL IC