Počet záznamů: 1  

Collagen-induced arthritis: severity and immune response attenuation using multivalent N-acetyl glucosamine

  1. 1.
    0435665 - MBÚ 2015 RIV GB eng J - Článek v odborném periodiku
    Richter, Jan - Čapková, Katarína - Hříbalová, Věra - Vannucci, Luca - Dányi, István - Malý, M. - Fišerová, Anna
    Collagen-induced arthritis: severity and immune response attenuation using multivalent N-acetyl glucosamine.
    Clinical and Experimental Immunology. Roč. 177, č. 1 (2014), s. 121-133. ISSN 0009-9104. E-ISSN 1365-2249
    Grant CEP: GA ČR GA310/06/0477; GA ČR GD310/08/H077
    Institucionální podpora: RVO:61388971
    Klíčová slova: CIA * clinical scoring * cytokines
    Kód oboru RIV: EC - Imunologie
    Impakt faktor: 3.037, rok: 2014

    Rheumatoid arthritis is an autoimmunity leading to considerable impairment of quality of life. N-acetyl glucosamine (GlcNAc) has been described previously as a potent modulator of experimental arthritis in animal models and is used for osteoarthritis treatment in humans, praised for its lack of adverse effects. In this study we present a comprehensive immunological analysis of multivalent GlcNAc-terminated glycoconjugate (GC) application in the treatment of collagen-induced arthritis (CIA) and its clinical outcome. We used immunohistochemistry and FACS to describe conditions on the inflammation site. Systemic and clinical effects were evaluated by FACS, cytotoxicity assay, ELISA, cytometric bead array (CBA), RT-PCR and clinical scoring. We found reduced inflammatory infiltration, NKG2D expression on NK and suppression of T, B and antigen-presenting cells (APC) in the synovia. On the systemic level, GCs prevented the activation of monocyte- and B cell-derived APCs, the rise of TNF- and IFN- levels, and subsequent type II collagen (CII)-specific IgG2a formation. Moreover, we detected an increase of anti-inflammatory IL-4 mRNA in the spleen. Similar to the synovia, the GCs caused a significant reduction of NKG2D-expressing NK cells in the spleen without influencing their lytic function.
    Trvalý link: http://hdl.handle.net/11104/0239621

     
     
Počet záznamů: 1  

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