Interleukin-1β and Interleukin-6 in Arthritis Animal Models: Roles in the Early Phase of Transition from Acute to Chronic Inflammation and Relevance for Human Rheumatoid Arthritis

被引:104
作者
Ferraccioli, Gianfranco [1 ]
Bracci-Laudiero, Luisa [2 ,3 ]
Alivernini, Stefano
Gremese, Elisa
Tolusso, Barbara
De Benedetti, Fabrizio [2 ]
机构
[1] Univ Cattolica Sacro Cuore, Div Rheumatol, Sch Med, CIC, I-00168 Rome, Italy
[2] Osped Pediat Bambin Gesu, Rome, Italy
[3] CNR, Inst Neurobiol & Mol Med, Rome, Italy
关键词
ANTIGEN-INDUCED ARTHRITIS; CYTOKINE MESSENGER-RNA; TUMOR-NECROSIS-FACTOR; T-CELL; LEUKOCYTE RECRUITMENT; AUTOIMMUNE ARTHRITIS; ADJUVANT ARTHRITIS; SOLUBLE RECEPTOR; GENE-EXPRESSION; SYNOVIAL-FLUID;
D O I
10.2119/molmed.2010.00067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Tumor necrosis factor-alpha (TNF-alpha) is the major target of the therapeutic approach in rheumatoid arthritis, A key issue in the approach to chronic arthritis is the understanding of the crucial molecules driving the transition from the acute phase to the chronic irreversible phase of the disease. In this review we analyzed five experimental arthritis animal models (antigen-induced arthritis, adjuvant-induced arthritis, streptococcal cell wall arthritis, collagen-induced arthritis and SKG) considered as possible scenarios to facilitate interpretation of the biology of human rheumatoid arthritis. The SKG model is strictly dependent on interleukin (IL)-6. In the other models, IL-1 beta and IL-6, more than TNF-alpha, appear to be relevant in driving the transition, which suggests that these should be the targets of an early intervention to stop the course toward the chronic form of the disease. (C) 2010 The Feinstein Institute for Medical Research, www.feinsteininstitute.org
引用
收藏
页码:552 / 557
页数:6
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