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完全弗氏佐剂可在MRL-lpr小鼠中诱发更早且更严重的关节炎。

Complete Freund's adjuvant induces an earlier and more severe arthritis in MRL-lpr mice.

作者信息

Ratkay L G, Zhang L, Tonzetich J, Waterfield J D

机构信息

Department of Oral Biology, Faculty of Dentistry, University of British Columbia, Vancouver, Canada.

出版信息

J Immunol. 1993 Nov 1;151(9):5081-7.

PMID:8409458
Abstract

A study was performed on the effect of CFA on the spontaneous arthritis of MRL-lpr mice. The development of swelling and erythema was monitored for 1 mo after injecting 13- to 14-wk-old mice intradermally with CFA, at which time the histopathology of the joints and serologic responses to extracellular matrix proteins were investigated. In a series of six experiments, 67 to 82% of mice showed early clinical evidence of arthritis in contrast to the low percentage observed in control animals. Similarly, the histopathologic analyses on the CFA-injected mice indicated a significantly higher frequency of advanced histopathologic alterations, characterized by cartilage erosion and pannus formation. The serologic evaluation of the adjuvant-injected mice demonstrated a significant enhanced antibody production to type I and type II collagens, DNA, and the Mycobacterium tuberculosis-positive control. This reproducible adjuvant-enhanced model of murine arthritis will be extremely useful in evaluating experimental therapeutic regimes as the arthritis is initiated earlier and exhibits an enhanced frequency and severity compared with the spontaneous arthritis seen in MRL-lpr mice.

摘要

开展了一项关于弗氏完全佐剂(CFA)对MRL - lpr小鼠自发性关节炎影响的研究。给13至14周龄的小鼠皮内注射CFA后,监测肿胀和红斑的发展情况1个月,此时对关节进行组织病理学检查,并研究对细胞外基质蛋白的血清学反应。在一系列六个实验中,67%至82%的小鼠出现了关节炎的早期临床证据,相比之下,在对照动物中观察到的比例较低。同样,对注射CFA小鼠的组织病理学分析表明,以软骨侵蚀和血管翳形成为特征的晚期组织病理学改变的频率显著更高。对注射佐剂小鼠的血清学评估显示,针对I型和II型胶原蛋白、DNA以及结核分枝杆菌阳性对照的抗体产生显著增强。这种可重复的佐剂增强型小鼠关节炎模型在评估实验性治疗方案方面将非常有用,因为与MRL - lpr小鼠中出现的自发性关节炎相比,该模型引发关节炎的时间更早,且频率和严重程度更高。

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