The Transformative Role of Mass Spectrometry in Diagnosing and Monitoring Monoclonal Gammopathies and Plasma Cell Disorders.

IF 1.9 Q3 MEDICAL LABORATORY TECHNOLOGY
Gema García de la Rosa, Silvia de Las Heras Flórez, Mercedes Carretero Pérez, Jorge Nuevo García
{"title":"The Transformative Role of Mass Spectrometry in Diagnosing and Monitoring Monoclonal Gammopathies and Plasma Cell Disorders.","authors":"Gema García de la Rosa, Silvia de Las Heras Flórez, Mercedes Carretero Pérez, Jorge Nuevo García","doi":"10.1093/jalm/jfaf133","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Mass spectrometry (MS) is emerging as a transformative diagnostic tool for plasma cell disorders, including multiple myeloma, Waldenström macroglobulinemia, and light chain amyloidosis. Traditional diagnostic methods such as serum protein electrophoresis, immunofixation electrophoresis, and serum free light chain assays, though effective, have limitations in sensitivity and specificity. These techniques may miss small monoclonal proteins or be affected by therapeutic antibody interference.</p><p><strong>Content: </strong>Recent advances focus on top-down MS techniques, particularly matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) and monoclonal immunoglobulin rapid accurate mass measurement (miRAMM). These methods analyze intact monoclonal proteins to enhance detection sensitivity and specificity. MALDI-TOF offers a streamlined workflow suitable for clinical laboratories, while miRAMM provides highly precise mass measurements, albeit requiring more sophisticated instrumentation.MS has demonstrated superior capabilities in detecting monoclonal proteins, including the ability to distinguish them from therapeutic antibodies. Additionally, MS enables structural characterization of monoclonal proteins, such as glycosylation patterns linked to amyloidosis. Notably, emerging evidence indicates that MS may match or surpass the sensitivity of molecular techniques. These include next-generation sequencing and next-generation flow cytometry, which are commonly applied to bone marrow biopsy for minimal residual disease detection, providing a less invasive alternative for disease monitoring.</p><p><strong>Summary: </strong>MS, particularly MALDI-TOF and miRAMM, represents a promising advancement in the diagnosis and monitoring of plasma cell disorders. Its high sensitivity, efficiency, and noninvasive nature support its potential to complement or replace existing diagnostic methods, improving patient care and clinical outcomes as the technology continues to evolve.</p>","PeriodicalId":46361,"journal":{"name":"Journal of Applied Laboratory Medicine","volume":" ","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Laboratory Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/jalm/jfaf133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Mass spectrometry (MS) is emerging as a transformative diagnostic tool for plasma cell disorders, including multiple myeloma, Waldenström macroglobulinemia, and light chain amyloidosis. Traditional diagnostic methods such as serum protein electrophoresis, immunofixation electrophoresis, and serum free light chain assays, though effective, have limitations in sensitivity and specificity. These techniques may miss small monoclonal proteins or be affected by therapeutic antibody interference.

Content: Recent advances focus on top-down MS techniques, particularly matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) and monoclonal immunoglobulin rapid accurate mass measurement (miRAMM). These methods analyze intact monoclonal proteins to enhance detection sensitivity and specificity. MALDI-TOF offers a streamlined workflow suitable for clinical laboratories, while miRAMM provides highly precise mass measurements, albeit requiring more sophisticated instrumentation.MS has demonstrated superior capabilities in detecting monoclonal proteins, including the ability to distinguish them from therapeutic antibodies. Additionally, MS enables structural characterization of monoclonal proteins, such as glycosylation patterns linked to amyloidosis. Notably, emerging evidence indicates that MS may match or surpass the sensitivity of molecular techniques. These include next-generation sequencing and next-generation flow cytometry, which are commonly applied to bone marrow biopsy for minimal residual disease detection, providing a less invasive alternative for disease monitoring.

Summary: MS, particularly MALDI-TOF and miRAMM, represents a promising advancement in the diagnosis and monitoring of plasma cell disorders. Its high sensitivity, efficiency, and noninvasive nature support its potential to complement or replace existing diagnostic methods, improving patient care and clinical outcomes as the technology continues to evolve.

质谱在诊断和监测单克隆伽玛病和浆细胞疾病中的变革作用。
背景:质谱(MS)正在成为一种变革性的浆细胞疾病诊断工具,包括多发性骨髓瘤、Waldenström巨球蛋白血症和轻链淀粉样变性。传统的诊断方法,如血清蛋白电泳、免疫固定电泳和血清游离轻链测定,虽然有效,但在敏感性和特异性方面存在局限性。这些技术可能会遗漏小的单克隆蛋白或受到治疗性抗体干扰的影响。内容:最近的进展集中在自上而下的质谱技术,特别是基质辅助激光解吸/电离飞行时间(MALDI-TOF)和单克隆免疫球蛋白快速精确质量测量(miRAMM)。这些方法分析完整的单克隆蛋白,提高了检测的灵敏度和特异性。MALDI-TOF提供了适合临床实验室的简化工作流程,而miRAMM提供了高度精确的质量测量,尽管需要更复杂的仪器。MS在检测单克隆蛋白方面表现出了卓越的能力,包括将它们与治疗性抗体区分开来的能力。此外,质谱能够对单克隆蛋白进行结构表征,例如与淀粉样变性相关的糖基化模式。值得注意的是,新出现的证据表明,质谱可能匹配或超过分子技术的灵敏度。其中包括下一代测序和下一代流式细胞术,它们通常应用于骨髓活检以检测最小残留疾病,为疾病监测提供了一种侵入性较小的替代方法。摘要:质谱,特别是MALDI-TOF和miRAMM,在浆细胞疾病的诊断和监测方面代表了一个有希望的进步。随着技术的不断发展,其高灵敏度、高效率和非侵入性支持了其补充或取代现有诊断方法的潜力,改善了患者护理和临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Applied Laboratory Medicine
Journal of Applied Laboratory Medicine MEDICAL LABORATORY TECHNOLOGY-
CiteScore
3.70
自引率
5.00%
发文量
137
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信