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改变的胶原蛋白II 263 - 272肽免疫通过向Th2型反应转变诱导对胶原诱导性关节炎的抑制。

Altered collagen II 263-272 peptide immunization induces inhibition of collagen-induced arthritis through a shift toward Th2-type response.

作者信息

Li R, Li X, Li Z

机构信息

Department of Rheumatology and Immunology, Peking University People's Hospital, 11 Xizhimen South Street, Beijing, China.

出版信息

Tissue Antigens. 2009 Apr;73(4):341-7. doi: 10.1111/j.1399-0039.2009.01223.x.

Abstract

To investigate the effects of altered collagen II (CII) peptide ligands in collagen-induced arthritis (CIA), CIA rats were subcutaneously injected with an altered CII263-272 peptide ligand (APL, 100, 10, and 1 microg/dose, six dose each, twice a week), which had been identified by us as an inhibitory effect on CII-specific T-cell activation in vitro in rheumatoid arthritis (RA). Clinical, radiographic, and histologic scores were evaluated. Serum level of interferon (IFN)-gamma was assessed by enzyme-linked immunosorbent assay, and the numbers of interleukin (IL)-4-producing cells in vitro in memory responses to the APL were determined by enzyme-linked immunospot. The results showed significantly reduced arthritis scores in CIA rats treated with 100 microg/dose of APL compared with those treated with phosphate buffered solution (PBS) and control peptide. The mean radiographic and histologic scores were also markedly lower in APL-treated CIA rats. On day 35 after immunization, a significantly lower level of IFN-gamma in serum was found in APL-treated rats, accompanied by increased numbers of IL-4-producing cells, indicating that APL treatment skewed the T helper (Th)1/Th2 balance toward Th2-type response in vivo. Altered CII263-272 peptide ligand immunization induces inhibition of CIA through a shift toward Th2-type response, suggesting that altered CII peptide might be a potential therapeutic target for RA.

摘要

为研究改变的胶原蛋白II(CII)肽配体在胶原诱导的关节炎(CIA)中的作用,给CIA大鼠皮下注射改变的CII263 - 272肽配体(APL,剂量分别为100、10和1微克/剂量,每种剂量6次,每周两次),我们已确定其在体外对类风湿关节炎(RA)中CII特异性T细胞活化具有抑制作用。评估临床、影像学和组织学评分。通过酶联免疫吸附测定法评估血清干扰素(IFN)-γ水平,并通过酶联免疫斑点法测定体外对APL记忆反应中产生白细胞介素(IL)-4的细胞数量。结果显示,与用磷酸盐缓冲溶液(PBS)和对照肽处理的大鼠相比,用100微克/剂量APL处理的CIA大鼠的关节炎评分显著降低。APL处理的CIA大鼠的平均影像学和组织学评分也明显较低。免疫后第35天,在APL处理的大鼠中发现血清中IFN-γ水平显著降低,同时产生IL-4的细胞数量增加,表明APL处理使体内辅助性T(Th)1/Th2平衡向Th2型反应倾斜。改变的CII263 - 272肽配体免疫通过向Th2型反应转变诱导对CIA的抑制,提示改变的CII肽可能是RA的潜在治疗靶点。

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