尿蛋白免疫固定电泳:游离轻链尿免疫固定电泳比常规检测单克隆轻链更敏感,可作为微量残留疾病的标志物。

Gurmukh Singh, Nkechi Arinze, David M Manthei, Frederick V Plapp, Roni J Bollag
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引用次数: 0

摘要

背景:血清和尿液中的免疫球蛋白单克隆轻链(MLCs)是单克隆γ -病变的标志物,可以作为多发性骨髓瘤(MM)最小残留病(MRD)的标志物。在以lc为主的mm患者中,尿中排出MLCs可导致肾脏损害和缩短生存期。方法:回顾性分析3个医疗中心的1738例尿液免疫固定标本,以评估尿液分析在单克隆γ病诊断和监测中的应用。我们采用改良的尿液免疫固定法检测了228份储存的尿液标本,使用抗血清检测游离lc (FLCs)。结果:我们对尿液免疫固定结果和医疗记录的回顾验证了唯一有意义的增值发现是检测单克隆自由轻链的理论。采用新方法检测的228份尿样,阳性结果增加18.4%。lambda LCs的增量发现率几乎是kappa LCs的3倍。结论:尿免疫固定法检测尿中MLCs的灵敏度和效率明显高于常规方法。新的分析似乎足够敏感,可以证明MLCs作为MM中MRD的标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Urine Protein Immunofixation Electrophoresis: Free Light Chain Urine Immunofixation Electrophoresis Is More Sensitive than Conventional Assays for Detecting Monoclonal Light Chains and Could Serve as a Marker of Minimal Residual Disease.

Background: Immunoglobulin monoclonal light chains (MLCs) in serum and urine are markers for monoclonal gammopathy and could serve as markers of minimal residual disease (MRD) in multiple myeloma (MM). Excretion of MLCs in urine is known to result in renal damage and shorter survival in patients with LC-predominant MM.

Methods: Retrospective review of urine immunofixation in 1738 specimens at 3 medical centers was conducted to assess the utility of urinalysis for diagnosis and monitoring of monoclonal gammopathy. We tested 228 stored urine specimens via the modified urine immunofixation method, using antisera to assay free LCs (FLCs).

Results: Our review of urine immunofixation results and medical records validated the theory that the only meaningful value-added finding was detection of monoclonal free light chains. Examination of 228 urine specimens using our novel method revealed 18.4% additional positive results. The rate of incremental findings for lambda LCs was nearly 3-fold higher than for kappa LCs.

Conclusions: The new method of urine immunofixation is significantly more sensitive and more efficient than the conventional method for detecting MLCs in urine. The new assay appears to be sensitive enough to prove that MLCs serve as a marker of MRD in MM.

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