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通过光密度法测量血清IgM和IgA单克隆蛋白的准确性。

Accuracy of serum IgM and IgA monoclonal protein measurements by densitometry.

作者信息

Tseng C Howard, Chang Chin-Yung, Liu Kevin S, Liu Frank J

机构信息

Department of Pathology, Chung Shan Medical University Hospital, Taichung, Taiwan.

出版信息

Ann Clin Lab Sci. 2003 Spring;33(2):160-6.

Abstract

We previously reported that proper dilution of sera that contain IgG monoclonal proteins (M-proteins) is necessary for accurate quantitation of serum albumin and M-protein concentrations separated by serum protein electrophoresis (SPE) using the Beckman PARAGON agarose electrophoresis system. We now report the significance of pre-electrophoretic serum dilution for M-protein quantitation of sera from patients with IgA and IgM monoclonal gammopathy. We measured M-proteins by SPE in 82 serum samples from 29 patients with IgA and 72 samples from 23 patients with IgM monodonal gammopathy. The serum M-protein concentrations (mean +/- SD) at 1:5, 1:10, and 1:20 dilutions (v/v) for all samples of both types were 49.7 +/- 12.9, 49.1 +/- 13.1, and 47.8 +/- 13.0 g/L, respectively. Thirty-two (20.8%) of 154 sera showed varying degrees of increase in M-protein concentrations with serum dilutions higher than 1:5; only 8 (5.2%) showed an increase 3 SDs. By SPE, the M-protein concentration (mean +/- SD) of these 8 sera at 1:5, 1:10, and 1:20 dilutions were 52.6 +/- 7.8, 57.1 +/- 7.2, and 57.6 +/- 7.1 g/L, respectively; the albumin concentrations (mean +/- SD) were 41.4 +/- 4.4, 37.9 +/- 3.8, and 37.1 +/- 2.9 g/L, respectively. The corresponding albumin concentration (mean +/- SD) was 36.8 +/- 3.7 g/L, assayed by the bromcresol green dye-binding method. These 8 samples were obtained from 3 patients, 2 with IgM kappa and 1 with IgA lambda monoclonal gammopathy. On the electrophoresis membranes, the M-protein bands of these 8 samples were narrow, thin, and dense; upon scanning, they appeared taller and thinner than the corresponding albumin bands. The samples of this subset contained relatively high concentrations of M-protein and total serum protein. We conclude that a pre-electrophoretic dilution of 1:5 (v/v) is adequate for most sera with IgA or IgM M-proteins. However, 1:10 or 1:20 dilution is occasionally required for a subset of sera with IgA or IgM M-proteins that show an unusually thin, narrow, and dense M-protein band and have high total serum protein content.

摘要

我们之前报道过,对于使用贝克曼PARAGON琼脂糖电泳系统通过血清蛋白电泳(SPE)分离的血清白蛋白和M蛋白浓度进行准确定量而言,适当稀释含有IgG单克隆蛋白(M蛋白)的血清是必要的。我们现在报告电泳前血清稀释对IgA和IgM单克隆丙种球蛋白病患者血清M蛋白定量的意义。我们通过SPE测量了来自29例IgA患者的82份血清样本和来自23例IgM单克隆丙种球蛋白病患者的72份血清样本中的M蛋白。两种类型所有样本在1:5、1:10和1:20稀释度(v/v)下的血清M蛋白浓度(均值±标准差)分别为49.7±12.9、49.1±13.1和47.8±13.0g/L。154份血清中有32份(20.8%)显示,血清稀释度高于1:5时M蛋白浓度有不同程度的升高;只有8份(5.2%)升高超过3个标准差。通过SPE,这8份血清在1:5、1:10和1:20稀释度下的M蛋白浓度(均值±标准差)分别为52.6±7.8、57.1±7.2和57.6±7.1g/L;白蛋白浓度(均值±标准差)分别为41.4±4.4、37.9±3.8和37.1±2.9g/L。通过溴甲酚绿染料结合法测定的相应白蛋白浓度(均值±标准差)为36.8±3.7g/L。这8个样本来自3例患者,2例为IgM κ型,1例为IgA λ型单克隆丙种球蛋白病。在电泳膜上,这8个样本的M蛋白条带窄、细且浓密;扫描时,它们比相应的白蛋白条带显得更高更窄。该亚组样本含有相对较高浓度的M蛋白和总血清蛋白。我们得出结论,对于大多数含有IgA或IgM M蛋白的血清,电泳前1:5(v/v)的稀释度就足够了。然而,对于一部分含有IgA或IgM M蛋白、M蛋白条带异常细窄浓密且总血清蛋白含量高的血清,偶尔需要1:10或1:20的稀释度。

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