McMaster Mary L, Csako Gyorgy
Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD MD 20892-7236, USA.
Int J Cancer. 2008 Mar 1;122(5):1183-8. doi: 10.1002/ijc.23229.
Protein electrophoresis is used for the detection, evaluation and follow-up of monoclonal gammopathy (MG) conditions such as Waldenström macroglobulinemia (WM). Immunofixation electrophoresis (IFE) is currently the most common method for isotyping of monoclonal gammopathy because of its superior sensitivity relative to immunoelectrophoresis (IEP). We designed a study to evaluate the clinicobiological relevance of small monoclonal bands detected by serum protein electrophoresis, IEP, and IFE. Serum protein electrophoresis, IEP, and IFE were used to evaluate possible monoclonal gammopathy in 46 members (29 relatives and 17 nonbloodline spouses) from 3 families with multiple cases of WM. IFE identified small monoclonal bands initially missed by IEP in 5 individuals (2 blood relatives, 3 spouses) among 46 study participants. All bands were IgM type. Twenty-three individuals, including the 2 blood relatives and 2 of 3 spouses with monoclonal gammopathy, were then followed for a median of 17 years (range, 13-25). The monoclonal gammopathy progressed in the 2 relatives but disappeared in the spouses, and new IgM MG developed in 2 additional relatives with a prior history of IgM polyclonal gammopathy. Small monoclonal bands detected by IFE in a familial context may be biologically meaningful, both as phenotypic biomarkers and possibly as predictors of high risk for WM. Polyclonal IgM may also be a marker of genetic susceptibility in WM families. Larger studies are needed to confirm these observations.
蛋白质电泳用于检测、评估和随访单克隆丙种球蛋白病(MG),如华氏巨球蛋白血症(WM)等情况。免疫固定电泳(IFE)因其相对于免疫电泳(IEP)具有更高的灵敏度,目前是单克隆丙种球蛋白病分型的最常用方法。我们设计了一项研究,以评估血清蛋白电泳、IEP和IFE检测到的小单克隆条带的临床生物学相关性。使用血清蛋白电泳、IEP和IFE对来自3个有多例WM患者的家庭的46名成员(29名亲属和17名非血缘配偶)进行可能的单克隆丙种球蛋白病评估。IFE在46名研究参与者中的5人(2名血亲、3名配偶)中识别出了最初被IEP遗漏的小单克隆条带。所有条带均为IgM型。然后对23人进行了随访,其中包括2名血亲以及3名患有单克隆丙种球蛋白病的配偶中的2名,随访时间中位数为17年(范围13 - 25年)。单克隆丙种球蛋白病在2名亲属中进展,但在配偶中消失,另外2名有IgM多克隆丙种球蛋白病病史的亲属出现了新的IgM MG。在家族背景下通过IFE检测到的小单克隆条带可能具有生物学意义,既作为表型生物标志物,也可能作为WM高风险的预测指标。多克隆IgM也可能是WM家族遗传易感性的标志物。需要更大规模的研究来证实这些观察结果。