Altered peptide ligands regulate type II collagen-induced arthritis in mice

被引:13
|
作者
Wakamatsu, Ei [1 ]
Matsumoto, Isao [1 ]
Yoshiga, Yohei [1 ]
Hayashi, Taichi [1 ]
Goto, Daisuke [1 ]
Ito, Satoshi [1 ]
Sumida, Takayuki [1 ]
机构
[1] Univ Tsukuba, Grad Sch Comprehens Human Sci, Doctoral Programs Med Sci, Div Clin Immunol, Tsukuba, Ibaraki 3058575, Japan
关键词
Altered peptide ligand; Antagonist; Type II collagen-induced arthritis; T cells; RHEUMATOID-ARTHRITIS; T-CELLS; IN-VIVO; SUPPRESSION; DETERMINANT; EXPANSION; ANALOG;
D O I
10.1007/s10165-009-0174-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We reported that peripheral blood mononuclear cells from HLA-DRB1*0101 Japanese patients with rheumatoid arthritis (RA) were highly reactive to 256-271 peptide of type II collagen (CII). Similar to RA, T cells reactive to CII (AA256-271) play a crucial role in the generation of arthritis in CII-induced arthritis mouse (I-A(q)). In the present study, we regulated the CII reactivity of T cells from CIA mouse with I-A(q) by altered peptide ligand (APL). Eight different APLs were designed and screened for their antagonistic activity using CII reactive cytokine production assay. Four APLs of CII 256-271 exhibited antagonistic activity in CII-reactive T cells. Moreover, intraperitoneally injected APL-5 (G262A) significantly suppressed CII-induced arthritis in mice, whereas the other three APLs did not. Compared with the control, APL-5 suppressed interleukin (IL)-17 production by T cells from CII-induced arthritis mice. These results suggest that CII APL is a potentially suitable therapeutic strategy for the control of RA.
引用
收藏
页码:366 / 371
页数:6
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