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Serum cytokine and chemokine profiles in patients with myasthenia gravis
Author(s) -
Uzawa A.,
Kawaguchi N.,
Himuro K.,
Kanai T.,
Kuwabara S.
Publication year - 2014
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12272
Subject(s) - myasthenia gravis , chemokine , immunology , medicine , cytokine , immune system
Summary Myasthenia gravis ( MG ) is an autoimmune‐mediated inflammatory disease of the neuromuscular junction. Previous studies of animal MG models have suggested important roles of cytokines in MG pathogenesis, but adequate studies on cytokines in human MG are lacking. Using a multiplex suspension array system, we measured the serum levels of 27 cytokines/chemokines in 47 anti‐acetylcholine receptor antibody‐positive patients with MG and 20 normal controls ( NC ) to investigate the contribution of cytokines/chemokines toward MG pathogenesis. Correlations between clinical parameters and cytokine/chemokine levels in patients with MG were also examined. The serum levels of interleukin ( IL )‐15 (mean ± standard deviation: 6·85 ± 6·97 pg/ml) and vascular endothelial growth factor ( VEGF ) (96·21 ± 71·60 pg/ml) significantly increased, whereas IL ‐4 levels (3·57 ± 0·86 pg/ml) decreased in patients with MG compared with NC ( IL ‐15: 4·42 ± 1·55 pg/ml; VEGF : 63·51 ± 32·95 pg/ml; IL ‐4: 4·15 ± 0·81 pg/ml, P  < 0·05). In addition, eight cytokines ( IL ‐4, IL ‐8, IL ‐15, eotaxin, macrophage inflammatory protein‐1α, macrophage inflammatory protein‐1β, VEGF and IL ‐1b) were significantly changed among MG patients with thymoma, MG patients without thymoma and NC ( P  < 0·05). Some cytokines, such as IL ‐4, IL ‐15, and VEGF , may play roles in the pathogenesis of MG .

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