β‐glucan triggers spondylarthritis and Crohn's disease–like ileitis in SKG mice

医学 指炎 关节炎 免疫学 柯德兰 回肠炎 末端炎 银屑病性关节炎 强直性脊柱炎 脊柱炎 炎性关节炎 克罗恩病 病理 疾病 生物 多糖 生物化学
作者
Merja Ruutu,Gethin Thomas,Roland Steck,Mariapia A. Degli‐Esposti,Martin S. Zinkernagel,Kylie A. Alexander,Jared Velasco,Geoffrey Strutton,Ai Tran,Helen Benham,Linda M. Rehaume,Robert J. Wilson,Kristine Kikly,Julian Davies,Allison R. Pettit,Matthew A. Brown,Michael A. McGuckin,Ranjeny Thomas
出处
期刊:Arthritis & Rheumatism [Wiley]
卷期号:64 (7): 2211-2222 被引量:252
标识
DOI:10.1002/art.34423
摘要

OBJECTIVE: The spondylarthritides (SpA), including ankylosing spondylitis (AS), psoriatic arthritis (PsA), reactive arthritis, and arthritis associated with inflammatory bowel disease, cause chronic inflammation of the large peripheral and axial joints, eyes, skin, ileum, and colon. Genetic studies reveal common candidate genes for AS, PsA, and Crohn's disease, including IL23R, IL12B, STAT3, and CARD9, all of which are associated with interleukin-23 (IL-23) signaling downstream of the dectin 1 β-glucan receptor. In autoimmune-prone SKG mice with mutated ZAP-70, which attenuates T cell receptor signaling and increases the autoreactivity of T cells in the peripheral repertoire, IL-17-dependent inflammatory arthritis developed after dectin 1-mediated fungal infection. This study was undertaken to determine whether SKG mice injected with 1,3-β-glucan (curdlan) develop evidence of SpA, and the relationship of innate and adaptive autoimmunity to this process. METHODS: SKG mice and control BALB/c mice were injected once with curdlan or mannan. Arthritis was scored weekly, and organs were assessed for pathologic features. Anti-IL-23 monoclonal antibodies were injected into curdlan-treated SKG mice. CD4+ T cells were transferred from curdlan-treated mice to SCID mice, and sera were analyzed for autoantibodies. RESULTS: After systemic injection of curdlan, SKG mice developed enthesitis, wrist, ankle, and sacroiliac joint arthritis, dactylitis, plantar fasciitis, vertebral inflammation, ileitis resembling Crohn's disease, and unilateral uveitis. Mannan triggered spondylitis and arthritis. Arthritis and spondylitis were T cell- and IL-23-dependent and were transferable to SCID recipients with CD4+ T cells. SpA was associated with collagen- and proteoglycan-specific autoantibodies. CONCLUSION: Our findings indicate that the SKG ZAP-70W163C mutation predisposes BALB/c mice to SpA, resulting from innate and adaptive autoimmunity, after systemic β-glucan or mannan exposure.
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