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ME 375

Molecular characterization of autoimmune polyglandular syndromes

Project goals

It is the goal of the submitted project to investigate a possible link of genetic predisposition and immunological features in autoimmune polyglandular syndromes (APS). One important question is whether or not clinically silent and overt forms of APS canbe differentiated by their genetic predisposition. The immunological studies will focus on both B- and T-cell mediated autoimmune responses. A broad range of recombinant antigens that were generated at IPM, Hamburg, can be used for a sensitive and specific diagnosis of APS. Because the T-cell mediated autoimmune response is crucial for the pathogenesis of APS the recombinant proteins also can be used for detection of autoreactive T-cells and the Th1/Th2-balance can be determined by ultrasensitive RT-PCR. Eventually, the specific detection of autoreactive T cells might have a great impact on future treatment of the autoimmune disease already in the subclinical state.

Keywords

autoimmune polyglandular syndromgenetic predispositionTh1/Th2-balance

Public support

  • Provider

    Ministry of Education, Youth and Sports

  • Programme

    KONTAKT

  • Call for proposals

    KONTAKT 1 (SMSM200132001)

  • Main participants

    Endokrinologický ústav

  • Contest type

    VS - Public tender

  • Contract ID

Alternative language

  • Project name in Czech

    Molekulární charakteristika autoimunitního poplyglandulálního syndromu

  • Annotation in Czech

    Cílem předloženého projektu je zjistit možnou vazbu mezi genedickou predizpozicí a rozvojem imunopatologických znaků u autoimunitního polyglandulárního syndromu (APS). Jednou z hlavních otázek je zda klinicky rozvinutý a nerozvinutý APS může mít odlišnosti v genetické predizpozici. Imunologické studie se zaměří na význam B a T lymfocytů v autoimunitním procesu.

Scientific branches

  • R&D category

  • CEP classification - main branch

    FB - Endocrinology, diabetology, metabolism, nutrition

  • CEP - secondary branch

    FN - Epidemiology, infection diseases and clinical immunology

  • CEP - another secondary branch

    FF - ENT (ie. ear, nose, throat), ophthalmology, dentistry

  • 30202 - Endocrinology and metabolism (including diabetes, hormones)
    30206 - Otorhinolaryngology
    30207 - Ophthalmology
    30208 - Dentistry, oral surgery and medicine
    30302 - Epidemiology
    30303 - Infectious Diseases

Completed project evaluation

  • Provider evaluation

    V - Vynikající výsledky projektu (s mezinárodním významem atd.)

  • Project results evaluation

    Exprese HLA antigenů ukazuje na genetickou rozdílnost mezi izolovanou autoimunitní tyreoiditidou a oběma skupinami s polyglandulárními projevy.

Solution timeline

  • Realization period - beginning

    Jan 1, 2000

  • Realization period - end

    Jan 1, 2002

  • Project status

    U - Finished project

  • Latest support payment

Data delivery to CEP

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

  • Data delivery code

    CEP/2003/MSM/MSM3ME/U/N/8:4

  • Data delivery date

    May 22, 2009

Finance

  • Total approved costs

    1,510 thou. CZK

  • Public financial support

    880 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    750 thou. CZK

Recognised costs

1 510 CZK thou.

Public support

880 CZK thou.

0%


Provider

Ministry of Education, Youth and Sports

CEP

FB - Endocrinology, diabetology, metabolism, nutrition

Solution period

01. 01. 2000 - 01. 01. 2002