McMaster Mary L, Kristinsson Sigurdur Y, Turesson Ingemar, Björkholm Magnus, Landgren Ola
Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Clin Lymphoma Myeloma. 2009 Mar;9(1):19-22. doi: 10.3816/CLM.2009.n.003.
Waldenström's macroglobulinemia (WM) is associated with a precursor condition, monoclonal gammopathy of undetermined significance (MGUS) of immunoglobulin-M (IgM) type. The etiology of these conditions is unknown. Recent studies at the population level have provided new data regarding familial aggregation of these disorders and other B-cell malignancies. Studies of familial clusters of WM have demonstrated an increased frequency of IgM MGUS compared with the general population and have provided new data suggesting that the phenotypic spectrum might also include polyclonal gammopathy and hypoglobulinemia. While the preponderance of immunoglobulin abnormalities in relatives of WM cases involves IgM, other immunoglobulin types (IgG and IgA) might also be affected. Large collaborative studies are needed to confirm these findings, which present an opportunity to define the earliest lesion(s) in the WM oncogenic pathway.
华氏巨球蛋白血症(WM)与一种前驱疾病相关,即免疫球蛋白M(IgM)型意义未明的单克隆丙种球蛋白病(MGUS)。这些疾病的病因尚不清楚。近期在人群层面的研究提供了关于这些疾病以及其他B细胞恶性肿瘤家族聚集性的新数据。对华氏巨球蛋白血症家族聚集情况的研究表明,与普通人群相比,IgM MGUS的发生率有所增加,并提供了新数据表明表型谱可能还包括多克隆丙种球蛋白病和低球蛋白血症。虽然华氏巨球蛋白血症病例亲属中免疫球蛋白异常大多涉及IgM,但其他免疫球蛋白类型(IgG和IgA)也可能受到影响。需要开展大型合作研究来证实这些发现,这为确定华氏巨球蛋白血症致癌途径中最早的病变提供了契机。