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抗 DNA 拓扑异构酶 I 抗体 IgM、IgG 和 IgA 在系统性硬化症中的作用。

IgM, IgG, and IgA anti-DNA topoisomerase I antibodies in systemic sclerosis.

机构信息

Laboratory of Research in Autoimmunity, Mexico.

出版信息

J Clin Lab Anal. 2009;23(6):408-16. doi: 10.1002/jcla.20342.

Abstract

BACKGROUND

Anti-DNA topoisomerase I (anti-topo I) antibodies have been broadly studied in systemic sclerosis (SSc). The use of different native and molecularly cloned antigens has shown a predominant IgG response, and a variable frequency of positive IgM and IgA tests. We report herein the serological findings of SSc using a recombinant topo I obtained through a standard bacterial system.

METHODS

Anti-topo I antibodies were studied in 45 SSc patients and 85 healthy controls through ELISA and western blot. Escherichia coli XL1-blue strain and pT7-7 vector were used to amplify a DNA topo I cDNA clone, and to obtain the recombinant polypeptide. The latter was purified by affinity chromatography, and the enzymatic and antigenic properties were evaluated through specific tests. A native antigen was included for comparison.

RESULTS

The SSc group disclosed positive IgM (20%), IgG (86.6%), and IgA (26.6%) anti-topo I tests with the recombinant polypeptide, and a purified calf thymus antigen yielded similar results. IgG autoantibodies were frequently associated with skin involvement, esophageal dysfunction, and restrictive lung disease. The recombinant protein showed a molecular weight of 86.6 kDa, a positive topo I activity using a supercoiled pBR322 DNA relaxation test, and its carboxyl terminus region was recognized by specific antibodies.

CONCLUSION

This report confirms that different immunoglobulin classes with anti-topo I activity may occur in SSc. IgG was the predominant serological feature with both, the recombinant and native antigens. The study also demonstrates the association between high levels of these autoantibodies and some clinical manifestations of SSc.

摘要

背景

抗 DNA 拓扑异构酶 I(抗-topo I)抗体已广泛研究于系统性硬化症(SSc)。使用不同的天然和分子克隆抗原已显示出主要的 IgG 反应,以及可变频率的阳性 IgM 和 IgA 测试。我们在此报告使用通过标准细菌系统获得的重组 topo I 的 SSc 的血清学发现。

方法

通过 ELISA 和 Western blot 研究了 45 例 SSc 患者和 85 例健康对照者的抗-topo I 抗体。Escherichia coli XL1-blue 菌株和 pT7-7 载体用于扩增 DNA topo I cDNA 克隆,并获得重组多肽。后者通过亲和层析进行纯化,并通过特异性试验评估其酶和抗原特性。包括天然抗原进行比较。

结果

SSc 组与重组多肽显示阳性 IgM(20%)、IgG(86.6%)和 IgA(26.6%)抗-topo I 测试,并且纯化的小牛胸腺抗原产生相似的结果。IgG 自身抗体常与皮肤受累、食管功能障碍和限制性肺病有关。重组蛋白显示分子量为 86.6 kDa,使用超螺旋 pBR322 DNA 松弛试验具有阳性 topo I 活性,并且其羧基末端区域被特异性抗体识别。

结论

本报告证实,具有抗-topo I 活性的不同免疫球蛋白类可能发生于 SSc 中。IgG 是主要的血清学特征,与重组和天然抗原均相关。该研究还表明这些自身抗体的高水平与 SSc 的一些临床表现之间存在关联。

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