José-Carreras-Center for Immuno- and Gene Therapy, Department Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Blood. 2011 Jul 21;118(3):635-7. doi: 10.1182/blood-2011-01-331454. Epub 2011 May 17.
Paratarg-7 (P-7) is a frequent paraprotein target in monoclonal gammopathy of undetermined significance (MGUS), multiple myeloma (MM), and Waldenström macroglobulinemia. Patients with P-7-specific paraproteins carry a hyperphosphorylated paratarg-7 (pP-7). Because pP-7 carrier state is dominantly inherited, we determined the paraprotein targets in 4 families with familial MGUS/MM. No antigenic target was identified for the paraproteins from 2 members of one family. Paraproteins from affected members of 2 other families targeted P-7, and paraproteins from 4 affected members of a fourth family targeted P-8, which is encoded by the ATG13 gene. P-8 was hyperphosphorylated in the affected family members (pP-8) and pP-8 carrier state is inherited in a dominant fashion. Six additional autoantigenic nonfamilial paraprotein targets were also hyperphosphorylated in the respective patients compared with normal controls. We conclude that paraproteins of affected members with familial MGUS/MM share family-typical hyperphosphorylated antigens and hyperphosphorylation of paraprotein targets might be a general mechanism underlying the pathogenesis of MGUS/MM.
ParaTarg-7 (P-7) 是单克隆丙种球蛋白病(MGUS)、多发性骨髓瘤(MM)和瓦尔登斯特伦巨球蛋白血症中常见的异常单克隆免疫球蛋白的靶标。具有 P-7 特异性副蛋白的患者携带高度磷酸化的 paraTarg-7 (pP-7)。由于 pP-7 携带状态是显性遗传的,我们确定了 4 个家族性 MGUS/MM 患者的副蛋白靶标。一个家族的 2 名成员的副蛋白没有确定抗原靶标。来自另外两个家族受影响成员的副蛋白靶向 P-7,来自第四个家族的 4 名受影响成员的副蛋白靶向由 ATG13 基因编码的 P-8。受影响的家族成员中的 P-8 被高度磷酸化(pP-8),并且 pP-8 携带状态以显性方式遗传。与正常对照相比,另外 6 个自身抗原性非家族性副蛋白靶标在各自的患者中也被高度磷酸化。我们得出结论,家族性 MGUS/MM 受影响成员的副蛋白具有家族典型的高度磷酸化抗原,并且副蛋白靶标的高度磷酸化可能是 MGUS/MM 发病机制的一般机制。