Therapeutic effect of low-dose IL-18 combined with IL-10 on collagen-induced arthritis by down-regulation of inflammatory and Th1 responses and induction of Th2 responses

被引:15
作者
Dai, Qiaomei [1 ,2 ]
Li, Yang [1 ]
Zhang, Fengshan [1 ]
Yu, Haiyue [1 ]
Wang, Xiaoyan [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Dept Rheumatol, Harbin 150081, Peoples R China
[2] Heilongjiang Univ Chinese Med, Dept Pathol, Harbin 150040, Peoples R China
基金
中国国家自然科学基金;
关键词
Interleukin-18; Collagen-induced arthritis; Interleukin-10; Th2; responses; RHEUMATOID-ARTHRITIS; IMMUNE-RESPONSES; SYNOVIAL TISSUE; INTERLEUKIN-18; EXPRESSION; CYTOKINES; ROLES; CELLS; MICE; IGE;
D O I
10.1007/s00296-008-0732-3
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
To investigate the anti-inflammatory or pleiotropic immunomodulatory role of interleukin-18 (IL-18), collagen-induced arthritis (CIA) mice were administrated with IL-18 along or in combination with IL-10, IL-4 or IL-12. IL-18 treatment along had no therapeutic effect on onset or established CIA mice. However, the combined treatment of low-dose IL-18 with IL-10 ameliorated the disease progression. Th1 cytokine expression was significantly inhibited, whereas Th2 cytokine expression was up-regulated in the synovial tissue by the IL-18/IL-10 treatment when compared with that in control group. Interestingly, IL-18 receptor (IL-18R) alpha expression was down-regulated by the treatment. According to the development of Th2 responses, GATA-3 mRNA expression was significantly increased in the treatment group. Our results indicated that combined treatment of low-dose IL-18 with IL-10 can prevent the development of CIA, which may be mediated not only by inhibiting Th1 responses through IL-18/IL-18R alpha signaling, but also by inducing anti-inflammatory mediators through a GATA-3-dependent mechanism.
引用
收藏
页码:615 / 622
页数:8
相关论文
共 30 条
[1]
Aita T, 2004, J RHEUMATOL, V31, P448
[2]
Interleukin-18 induces angiogenic factors in rheumatoid arthritis synovial tissue fibroblasts via distinct signaling pathways [J].
Amin, Mohammad A. ;
Mansfield, Pamela J. ;
Pakozdi, Angela ;
Campbell, Phillip L. ;
Ahmed, Salahuddin ;
Martinez, Rita J. ;
Koch, Alisa E. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (06) :1787-1797
[3]
Dysregulation of interleukin-10-dependent gene expression in rheumatoid arthritis synovial macrophages [J].
Antoniv, Taras T. ;
Ivashkiv, Lionel B. .
ARTHRITIS AND RHEUMATISM, 2006, 54 (09) :2711-2721
[4]
Prevention of collagen-induced arthritis in mice transgenic for the complement inhibitor complement receptor 1-related gene/protein y [J].
Banda, NK ;
Kraus, DM ;
Muggli, M ;
Bendele, A ;
Holers, VM ;
Arend, WP .
JOURNAL OF IMMUNOLOGY, 2003, 171 (04) :2109-2115
[5]
Role of GATA-3 in allergic diseases [J].
Barnes, Peter J. .
CURRENT MOLECULAR MEDICINE, 2008, 8 (05) :330-334
[6]
BRAND DD, 2007, IMMUNOLOGY, V122, P210, DOI DOI 10.1111/J.1365-2567.2007.02630.X
[7]
T-bet/GATA-3 ratio as a measure of the Th1/Th2 cytokine profile in mixed cell populations: predominant role of GATA-3 [J].
Chakir, H ;
Wang, HP ;
Lefebvre, DE ;
Webb, J ;
Scott, FW .
JOURNAL OF IMMUNOLOGICAL METHODS, 2003, 278 (1-2) :157-169
[8]
Cellular targets of interleukin-18 in rheumatoid arthritis [J].
Dai, Sheng-Ming ;
Shan, Zheng-Zheng ;
Xu, Huji ;
Nishioka, Kusuki .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (11) :1411-1418
[9]
Interleukin-18 enhances monocyte tumor necrosis factor α and interleukin-1β production induced by direct contact with T lymphocytes -: Implications in rheumatoid arthritis [J].
Dai, SM ;
Matsuno, H ;
Nakamura, H ;
Nishioka, K ;
Yudoh, K .
ARTHRITIS AND RHEUMATISM, 2004, 50 (02) :432-443
[10]
Role of cytokines in rheumatoid arthritis: an education in pathophysiology and therapeutics [J].
Feldmann, Marc ;
Maini, Ravinder N. .
IMMUNOLOGICAL REVIEWS, 2008, 223 :7-19