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水溶性非变性 II 型胶原蛋白可改善胶原诱导的关节炎小鼠的病情。

Water-soluble undenatured type II collagen ameliorates collagen-induced arthritis in mice.

机构信息

1 Development Division, Ryusendo Co. Ltd. , Toshimaku, Tokyo, Japan .

出版信息

J Med Food. 2013 Nov;16(11):1039-45. doi: 10.1089/jmf.2013.2911. Epub 2013 Oct 31.

Abstract

Earlier studies have reported the efficacy of type II collagen (C II) in treating rheumatoid arthritis (RA). However, a few studies have investigated the ability of the antigenic collagen to induce oral tolerance, which is defined as active nonresponse to an orally administered antigen. We hypothesized that water-soluble undenatured C II had a similar effect as C II in RA. The present study was designed to examine the oral administration of a novel, water-soluble, undenatured C II (commercially known as NEXT-II) on collagen-induced arthritis (CIA) in mice. In addition, the underlying mechanism of NEXT-II was also identified. After a booster dose (collagen-Freund's complete adjuvant), mice were assigned to control CIA group, or NEXT-II treatment group, to which saline and NEXT-II were administered, respectively. The arthritis index in the NEXT-II group was significantly lower compared with the CIA group. Serum IL-6 levels in the NEXT-II group were significantly lower compared with the CIA group, while serum IL-2 level was higher. Furthermore, oral administration of NEXT-II enhanced the proportion of CD4+CD25+T (Treg) cells, and gene expressions of stimulated dendritic cells induced markers for regulatory T cells such as forkhead box p3 (Foxp3), transforming growth factor (TGF)-β1, and CD25. These results demonstrated that orally administered water-soluble undenatured C II (NEXT-II) is highly efficacious in the suppression of CIA by inducing CD4+CD25+ Treg cells.

摘要

早期研究报告了 II 型胶原蛋白(C II)在治疗类风湿关节炎(RA)方面的疗效。然而,少数研究调查了抗原胶原蛋白诱导口服耐受的能力,口服耐受定义为对口服给予的抗原的主动无反应。我们假设水溶性未变性 C II 具有与 RA 中 C II 相似的作用。本研究旨在研究新型水溶性未变性 C II(商业上称为 NEXT-II)对胶原诱导性关节炎(CIA)小鼠的口服给药作用。此外,还确定了 NEXT-II 的潜在机制。在加强剂量(胶原-Freund 完全佐剂)后,将小鼠分为对照 CIA 组或 NEXT-II 治疗组,分别给予生理盐水和 NEXT-II。与 CIA 组相比,NEXT-II 组的关节炎指数明显降低。NEXT-II 组的血清 IL-6 水平明显低于 CIA 组,而血清 IL-2 水平升高。此外,口服 NEXT-II 增强了 CD4+CD25+T(Treg)细胞的比例,并且刺激树突状细胞的基因表达诱导了调节性 T 细胞的标志物,如叉头框 p3(Foxp3)、转化生长因子(TGF)-β1 和 CD25。这些结果表明,口服给予水溶性未变性 C II(NEXT-II)通过诱导 CD4+CD25+Treg 细胞在抑制 CIA 方面非常有效。

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