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改变的肽配体调节小鼠II型胶原诱导的关节炎。

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

作者信息

Wakamatsu Ei, Matsumoto Isao, Yoshiga Yohei, Hayashi Taichi, Goto Daisuke, Ito Satoshi, Sumida Takayuki

机构信息

Division of Clinical Immunology, Doctoral Programs in Medical Sciences, Major of Advanced Biomedical Applications, Graduate School Comprehensive Human Science, University of Tsukuba, 1-1-1 Tenodai, Tsukuba, Ibaraki 305-8575, Japan.

出版信息

Mod Rheumatol. 2009;19(4):366-71. doi: 10.1007/s10165-009-0174-0. Epub 2009 May 12.

Abstract

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.

摘要

我们报道,来自携带HLA - DRB1*0101的日本类风湿关节炎(RA)患者的外周血单个核细胞对II型胶原(CII)的256 - 271肽具有高度反应性。与RA相似,对CII(AA256 - 271)反应的T细胞在CII诱导的关节炎小鼠(I - A(q))的关节炎发生中起关键作用。在本研究中,我们通过改变肽配体(APL)来调节来自I - A(q)的CIA小鼠T细胞的CII反应性。设计了八种不同的APL,并使用CII反应性细胞因子产生测定法筛选它们的拮抗活性。四种CII 256 - 271的APL在CII反应性T细胞中表现出拮抗活性。此外,腹腔注射APL - 5(G262A)显著抑制小鼠CII诱导的关节炎,而其他三种APL则没有。与对照组相比,APL - 5抑制了CII诱导关节炎小鼠T细胞产生白细胞介素(IL)-17。这些结果表明,CII APL是控制RA的一种潜在合适的治疗策略。

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