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Optimal Tolerogenic Dendritic Cells in Type 1 Diabetes (T1D) Therapy: What Can We Learn From Non-obese Diabetic (NOD) Mouse Models?

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    SYSNO ASEP0505825
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleOptimal Tolerogenic Dendritic Cells in Type 1 Diabetes (T1D) Therapy: What Can We Learn From Non-obese Diabetic (NOD) Mouse Models?
    Author(s) Funda, David P. (MBU-M) RID, ORCID
    Palová-Jelinková, L. (CZ)
    Goliáš, Jaroslav (MBU-M) RID
    Kroulíková, Zuzana (MBU-M)
    Fajstová, Alena (MBU-M) ORCID
    Hudcovic, Tomáš (MBU-M) RID, ORCID
    Spíšek, R. (CZ)
    Article number967
    Source TitleFrontiers in Immunology. - : Frontiers Media - ISSN 1664-3224
    Roč. 10, MAY 14 (2019)
    Number of pages14 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordstype 1 diabetes ; cell therapy ; animal models
    Subject RIVEE - Microbiology, Virology
    OECD categoryMicrobiology
    R&D ProjectsNV16-27994A GA MZd - Ministry of Health (MZ)
    Method of publishingOpen access
    Institutional supportMBU-M - RVO:61388971
    UT WOS000467844100001
    EID SCOPUS85067271405
    DOI10.3389/fimmu.2019.00967
    AnnotationTolerogenic dendritic cells (tolDCs) are explored as a promising standalone or combination therapy in type 1 diabetes (T1D). The therapeutic application of tolDCs, including in human trials, has been tested also in other autoimmune diseases, however, T1D displays some unique features. In addition, unlike in several disease-induced animal models of autoimmune diseases, the prevalent animal model for T1D, the NOD mouse, develops diabetes spontaneously. This review compares evidence of various tolDCs approaches obtained from animal (mainly NOD) models of T1D with a focus on parameters of this cell-based therapy such as protocols of tolDC preparation, antigen-specific vs. unspecific approaches, doses of tolDCs and/or autoantigens, application schemes, application routes, the migration of tolDCs as well as their preventive, early pre-onset intervention or curative effects. This review also discusses perspectives of tolDC therapy and areas of preclinical research that are in need of better clarification in animal models in a quest for effective and optimal tolDC therapies of T1D in humans.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2020
    Electronic addresshttps://www.frontiersin.org/articles/10.3389/fimmu.2019.00967/full
Number of the records: 1  

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