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通过既定的酶联免疫吸附测定(ELISA)系统检测血清IgG4水平及其在自身免疫性疾病中的临床应用。

Measurement of serum IgG4 levels by an established ELISA system and its clinical applications in autoimmune diseases.

作者信息

Sun Wei, Gao Rong-Fen, Chen Yu, Su Yu-Ying, Dong Ling-Li

机构信息

Department of Stomatology, Union Hospital, Huazhong University of Science and Technology, Wuhan, 430022, China.

Department of Rheumatology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, 430030, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2013 Aug;33(4):611-614. doi: 10.1007/s11596-013-1167-y. Epub 2013 Aug 1.

Abstract

IgG4-related disease (IgG4-RD) is a novel and rare autoimmune disease entity. Elevated serum IgG4 level is strongly suggestive of IgG4-RD. But it is still unknown whether serum IgG4 elevation commonly occurs in other autoimmune diseases. In this study, the serum IgG4 levels were detected by an established enzyme-linked immunosorbent assay (ELISA) in a variety of autoimmune diseases including systemic lupus erythematosus (SLE), Sjogren's syndrome (SS), polymyositis or dermatomyositis (PM/DM) and IgG4-RD. To evaluate the reliability of this ELISA system, some of our samples were sent to a lab in Kanazawa Medical University, Japan, and detected by using the nephelometric assay. The results showed that our findings were consistent with theirs. Moreover, it was found that the serum IgG4 levels were 0.23±0.16 g/L in 53 healthy controls, 0.16±0.15 g/L in 103 SLE patients, 0.22±0.18 g/L in 41 SS patients and 0.40±0.32 g/L in 21 PM/DM patients. No significant difference in the serum IgG4 level was observed among these groups (P>0.05). The serum IgG4 levels of two cases of IgG4-RD were 1.63 and 4.65 g/L respectively, and both decreased markedly after treatment with glucocorticoids. These data indicated that this established ELISA system can be used for detecting serum IgG4 levels. Elevated serum IgG4 levels help diagnose IgG4-RD and evaluate the curative effect of this condition rather than other autoimmune diseases.

摘要

IgG4相关性疾病(IgG4-RD)是一种新型罕见的自身免疫性疾病实体。血清IgG4水平升高强烈提示IgG4-RD。但血清IgG4升高是否常见于其他自身免疫性疾病仍不清楚。在本研究中,采用已建立的酶联免疫吸附测定(ELISA)法检测了包括系统性红斑狼疮(SLE)、干燥综合征(SS)、多发性肌炎或皮肌炎(PM/DM)以及IgG4-RD在内的多种自身免疫性疾病患者的血清IgG4水平。为评估该ELISA系统的可靠性,我们将部分样本送至日本金泽医科大学的一个实验室,采用散射比浊法进行检测。结果显示我们的发现与他们的一致。此外,发现53名健康对照者的血清IgG4水平为0.23±0.16 g/L,103名SLE患者为0.16±0.15 g/L,41名SS患者为0.22±0.18 g/L,21名PM/DM患者为0.40±0.32 g/L。这些组间血清IgG4水平未观察到显著差异(P>0.05)。2例IgG4-RD患者的血清IgG4水平分别为1.63和4.65 g/L,经糖皮质激素治疗后均显著下降。这些数据表明该已建立的ELISA系统可用于检测血清IgG4水平。血清IgG4水平升高有助于诊断IgG4-RD并评估该病的治疗效果,而非用于其他自身免疫性疾病。

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