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

被引:208
作者
Ruutu, Merja
Thomas, Gethin
Steck, Roland [2 ]
Degli-Esposti, Mariapia A. [4 ]
Zinkernagel, Martin S. [4 ]
Alexander, Kylie [3 ]
Velasco, Jared
Strutton, Geoffrey
Ai Tran
Benham, Helen
Rehaume, Linda
Wilson, Robert J. [3 ]
Kikly, Kristine [5 ]
Davies, Julian [6 ]
Pettit, Allison R. [3 ]
Brown, Matthew A.
McGuckin, Michael A. [7 ]
Thomas, Ranjeny [1 ]
机构
[1] Univ Queensland, Diamantina Inst, Princess Alexandra Hosp, Brisbane, Qld 4102, Australia
[2] Queensland Univ Technol, Brisbane, Qld 4001, Australia
[3] Royal Brisbane & Womens Hosp, Brisbane, Qld, Australia
[4] Lions Eye Inst, Nedlands, WA, Australia
[5] Eli Lilly & Co, Indianapolis, IN 46285 USA
[6] Eli Lilly, Lilly Biotechnol Ctr San Diego, San Diego, CA USA
[7] Mater Med Res Inst, Brisbane, Qld, Australia
来源
ARTHRITIS AND RHEUMATISM | 2012年 / 64卷 / 07期
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
T-CELL SELECTION; ANKYLOSING-SPONDYLITIS; AUTOIMMUNE ARTHRITIS; INFLAMMATORY DISEASE; DENDRITIC CELLS; TH17; CELLS; HLA-B27; ANTIBODIES; RELEVANCE; RECEPTOR;
D O I
10.1002/art.34423
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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 beta-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-17dependent inflammatory arthritis developed after dectin 1mediated fungal infection. This study was undertaken to determine whether SKG mice injected with 1,3-beta-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. AntiIL-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-23dependent 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 beta-glucan or mannan exposure.
引用
收藏
页码:2211 / 2222
页数:12
相关论文
共 49 条
[1]   IgG antibodies against common gut bacteria are more diagnostic for Crohn's disease than IgG against mannan or flagellin [J].
Adams, Rachel J. ;
Heazlewood, Sharise P. ;
Gilshenan, Kristen S. ;
O'Brien, Mark ;
McGuckin, Michael A. ;
Florin, Timothy H. J. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (02) :386-396
[2]   Analysis of IL-17+ cells in facet joints of patients with spondyloarthritis suggests that the innate immune pathway might be of greater relevance than the Th17-mediated adaptive immune response [J].
Appel, Heiner ;
Maier, Rene ;
Wu, Peihua ;
Scheer, Rebecca ;
Hempfing, Axel ;
Kayser, Ralph ;
Thiel, Andreas ;
Radbruch, Andreas ;
Loddenkemper, Christoph ;
Sieper, Joachim .
ARTHRITIS RESEARCH & THERAPY, 2011, 13 (03)
[3]   Mesenchymal cell targeting by TNF as a common pathogenic principle in chronic inflammatory joint and intestinal diseases [J].
Armaka, Maria ;
Apostolaki, Maria ;
Jacques, Peggy ;
Kontoyiannis, Dimitris L. ;
Elewaut, Dirk ;
Kollias, George .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (02) :331-337
[4]   Anti-Saccharomyces cerevisiae antibodies (ASCA) in spondyloarthropathies:: a reassessment [J].
Aydin, S. Z. ;
Atagunduz, P. ;
Temel, M. ;
Bicakcigil, M. ;
Tasan, D. ;
Direskeneli, H. .
RHEUMATOLOGY, 2008, 47 (02) :142-144
[5]  
Benjamin M, 2009, ADV EXP MED BIOL, V649, P57
[6]   Th1/Th17 polarization and acquisition of an arthritogenic phenotype in arthritis-susceptible BALB/c, but not in MHC-matched, arthritis-resistant DBA/2 mice [J].
Boldizsar, Ferenc ;
Tarjanyi, Oktavia ;
Nemeth, Peter ;
Mikecz, Katalin ;
Glant, Tibor T. .
INTERNATIONAL IMMUNOLOGY, 2009, 21 (05) :511-522
[7]   Balancing inflammation and tolerance in vivo through dendritic cells by the commensal Candida albicans [J].
Bonifazi, P. ;
Zelante, T. ;
D'Angelo, C. ;
De Luca, A. ;
Moretti, S. ;
Bozza, S. ;
Perruccio, K. ;
Iannitti, R. G. ;
Giovannini, G. ;
Volpi, C. ;
Fallarino, F. ;
Puccetti, P. ;
Romani, L. .
MUCOSAL IMMUNOLOGY, 2009, 2 (04) :362-374
[8]   Susceptibility to ankylosing spondylitis in twins - The role of genes, HLA, and the environment [J].
Brown, MA ;
Kennedy, LG ;
MacGregor, AJ ;
Darke, C ;
Duncan, E ;
Shatford, JL ;
Taylor, A ;
Calin, A ;
Wordsworth, P .
ARTHRITIS AND RHEUMATISM, 1997, 40 (10) :1823-1828
[9]   Autoimmune Regulator Controls T Cell Help for Pathogenetic Autoantibody Production in Collagen-Induced Arthritis [J].
Campbell, Ian K. ;
Kinkel, Sarah A. ;
Drake, Sarah F. ;
van Nieuwenhuijze, Annemarie ;
Hubert, Francois-Xavier ;
Tarlinton, David M. ;
Heath, William R. ;
Scott, Hamish S. ;
Wicks, Ian P. .
ARTHRITIS AND RHEUMATISM, 2009, 60 (06) :1683-1693
[10]   HLA-B27 positive patients differ from HLA-B27 negative patients in clinical presentation and imaging: results from the DESIR cohort of patients with recent onset axial spondyloarthritis [J].
Chung, Ho Yin ;
Machado, Pedro ;
van der Heijde, Desiree ;
D'Agostino, Maria-Antonietta ;
Dougados, Maxime .
ANNALS OF THE RHEUMATIC DISEASES, 2011, 70 (11) :1930-1936