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使用红外荧光成像系统(IFIS)建立一种简单的定量免疫斑点分析方法来检测抗II型胶原抗体。

Establishment of a simple and quantitative immunospot assay for detecting anti-type II collagen antibody using an infrared fluorescence imaging system (IFIS).

作者信息

Ota Shusuke, Kanazawa Satoshi, Kobayashi Masaaki, Otsuka Takanobu, Okamoto Takashi

机构信息

Department of Molecular and Cellular Biology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.

出版信息

J Immunol Methods. 2005 Apr;299(1-2):189-98. doi: 10.1016/j.jim.2005.03.002. Epub 2005 Apr 7.

Abstract

Antibodies to type II collagen (col II) have been detected in patients with rheumatoid arthritis and in animal models of collagen induced arthritis. Here, we describe a novel method to detect anti-col II antibodies using an immunospot assay with an infrared fluorescence imaging system. This method showed very high sensitivity and specificity, and was simple, with low background levels. It also showed higher reproducibility and linearity, with a dynamic range of approximately 500-fold, than the conventional immunospot assay with enhanced chemiluminescence detection. Using this method we were able to demonstrate the antibody affinity maturation process in mice immunized with col II. In these immunized mice, although cross-reactive antibodies reacting with other collagen species were detected in earlier stages of immunization, the titers of cross-reactive antibodies rapidly diminished after the antigen boost, concomitantly with the elevation of the anti-col II antibody. The method and its possible applications are discussed.

摘要

在类风湿性关节炎患者及胶原诱导性关节炎动物模型中已检测到抗II型胶原(col II)抗体。在此,我们描述了一种使用红外荧光成像系统的免疫斑点分析法来检测抗col II抗体的新方法。该方法显示出非常高的灵敏度和特异性,操作简单,背景水平低。与传统的增强化学发光检测免疫斑点分析法相比,它还具有更高的重现性和线性,动态范围约为500倍。使用该方法,我们能够证明用col II免疫的小鼠体内抗体亲和力成熟过程。在这些免疫小鼠中,尽管在免疫早期检测到了与其他胶原种类发生交叉反应的抗体,但在抗原增强后,交叉反应抗体的滴度迅速下降,同时抗col II抗体升高。本文讨论了该方法及其可能的应用。

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