ESID Prague Spring Meeting 2008 – programme:
Monday morning , May 19: optional programme - UniversityHospital Motol
10am-10.30amRegistration
10.30am-10.45amOpening welcome speech
10.45am-11.15amPresentation of sponsors
11.15am-11.45amOptional visit of departments - Institute of Immunology, laboratory
settings, Department of Pediatrics, newly opened facilities, transplantation unit
12am-12.30pmTransportation to Olympus, official venue site
Monday afternoon, May 19: scientific programme - Olympus
12.30pm-1.30pmRegistration, lunch in Olympus, official venue site
1.30pm-3pmManagement of PIDs
Andrew Cant (invited speaker):BMT in PIDs, cord blood transplants (40 min).
Peter Čižnár: BMT in SCID patients in Slovakia (10 min).
Renata Formánková: Stem Cell Transplantation for Chronic Granulomatous Disease in Czech Republic – First Experience (10 min).
Svetlana Shchebet: Development of immunological and genetic diagnostic in patients with primary immunodeficiency in Belarus (15min).
Radana Zachová: Patiens with primary immunodeficiencies in Prague (5 min).
Vilma Mulaosmanovic: The situation in PID in Bosnia and Herzegovina (5 min).
Mariela Milla Pimentel: The situation in PID in Lima, Peru (5 min).
3.15pm-4.30pmT cells and severe immunodeficiences
Graham Davies (invited speaker): Di George syndrome (45min).
Olesya Shvets: Revealing Children with Di George syndrome (15min).
Anna Šedivá: T-reg in patients with Di George syndrome (10min).
Tuesday morning, May 20:
9am-10.30amB cells, other immunodeficiences
Alison Jones (invited speaker): Immunoglobulin replacement therapy in PIDs (40min).
Jiří Litzman: Mannose-binding lectin (MBL) variants in CVID (15min).
Christian Forster: Calcium signaling in B and T lymphocytes of patients with CVID (15min).
Lucie Grodecká, Hana Grombiříková, Jiří Litzman, Tomáš Freiberger: C1 inhibitor gene promoter mutations: potential role in hereditary angioedema development (15min).
10.30am10.45amCoffee Break
10.45am-12amB cells, other immunodeficiences
Tomáš Freiberger: Spectrum of the BTK gene mutations inCzech XLA patiens (10 min).
Baerbel Keller: CD21low B cells – an activated B cell population exposed to type I interferon (15min)
Zita Trávníčková: Functional testing of antibody production on the B cell level (10 min).
Vojtěch Thon: The European study of distinct clinical phenotypes of Common Variable Immunodeficiency Disorders (15 min).
12am-1pmLunch
1pm-3pmInnate immunity and regulatory defects
Eleonora Gambinieri (ESID Juniors): IPEX – genotype/phenotype correlation, hints for the diagnosis and overview on therapeutic approaches (45min)
Marco Gattorno: Diagnosis and Management of Autoinflammatory Diseases in Childhood (45min).
Andrea Poloučková: Early onset sarcoidosis – case report (10 min).
Nadine Voelxen: Defective activation and signaling of B cells in persistent polyclonal B cell lymphocytosis (PPBL) (10min)
Jeannet Botros: Pattern of Chediak Higashi Syndrome in Egyptian Children: A variant with Hyperpigmentation of the skin and a subtle clinical course (10min)
3pm-3.15pm Coffee Break
3.15pm-4.30pmCase reports and Varia
Mariela Milla Pimentel: Atopic Dermatitis vs Hyper IgE syndrome (15 min).
Filomeen Haerynck: Disseminated Mycobacterium avium infection in a patient with a novel mutation in the interleukin 12RB1 chain (20min)
Hana Kayserová.: Ourexperiences with the interferon-gama treatment in patients with Chronic granulomatous disease (10min)
Pařízková, Rozsíval: A boy with chronic EBV disease and hypogammaglobulinaemia - suspected XLP-ID disease (10 min).
Aleš Janda: Intractable colitis with immunodeficiency of unknown cause in an infant (15min)