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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.
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页码:366 / 371
页数:6
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