Hospital Universitario de Salamanca, Salamanca, Spain.
Haematologica. 2013 Jan;98(1):79-86. doi: 10.3324/haematol.2012.067272. Epub 2012 Jul 6.
Multiple myeloma remains largely incurable. However, a few patients experience more than 10 years of relapse-free survival and can be considered as operationally cured. Interestingly, long-term disease control in multiple myeloma is not restricted to patients with a complete response, since some patients revert to having a profile of monoclonal gammopathy of undetermined significance. We compared the distribution of multiple compartments of lymphocytes and dendritic cells in the bone marrow and peripheral blood of multiple myeloma patients with long-term disease control (n=28), patients with newly diagnosed monoclonal gammopathy of undetermined significance (n=23), patients with symptomatic multiple myeloma (n=23), and age-matched healthy adults (n=10). Similarly to the patients with monoclonal gammopathy of undetermined significance and symptomatic multiple myeloma, patients with long-term disease control showed an expansion of cytotoxic CD8(+) T cells and natural killer cells. However, the numbers of bone marrow T-regulatory cells were lower in patients with long-term disease control than in those with symptomatic multiple myeloma. It is noteworthy that B cells were depleted in patients with monoclonal gammopathy of undetermined significance and in those with symptomatic multiple myeloma, but recovered in both the bone marrow and peripheral blood of patients with long-term disease control, due to an increase in normal bone marrow B-cell precursors and plasma cells, as well as pre-germinal center peripheral blood B cells. The number of bone marrow dendritic cells and tissue macrophages differed significantly between patients with long-term disease control and those with symptomatic multiple myeloma, with a trend to cell count recovering in the former group of patients towards levels similar to those found in healthy adults. In summary, our results indicate that multiple myeloma patients with long-term disease control have a constellation of unique immune changes favoring both immune cytotoxicity and recovery of B-cell production and homing, suggesting improved immune surveillance.
多发性骨髓瘤在很大程度上仍然无法治愈。然而,少数患者经历了 10 年以上的无复发生存时间,可以被认为是临床治愈。有趣的是,多发性骨髓瘤的长期疾病控制并不仅限于完全缓解的患者,因为一些患者会恢复到单克隆丙种球蛋白血症的意义不明的表现。我们比较了长期疾病控制(n=28)、新诊断的意义不明的单克隆丙种球蛋白血症(n=23)、有症状的多发性骨髓瘤(n=23)和年龄匹配的健康成年人(n=10)患者骨髓和外周血中多个淋巴细胞和树突状细胞隔室的分布。与意义不明的单克隆丙种球蛋白血症和有症状的多发性骨髓瘤患者相似,长期疾病控制的患者表现出细胞毒性 CD8+T 细胞和自然杀伤细胞的扩增。然而,长期疾病控制患者的骨髓 T 调节细胞数量低于有症状的多发性骨髓瘤患者。值得注意的是,意义不明的单克隆丙种球蛋白血症和有症状的多发性骨髓瘤患者的 B 细胞耗竭,但在长期疾病控制患者的骨髓和外周血中都恢复了,这是由于正常骨髓 B 细胞前体和浆细胞以及生发中心前体外周血 B 细胞的增加。长期疾病控制患者的骨髓树突状细胞和组织巨噬细胞数量与有症状的多发性骨髓瘤患者有显著差异,前者的细胞计数有向健康成年人相似水平恢复的趋势。总之,我们的结果表明,长期疾病控制的多发性骨髓瘤患者具有独特的免疫变化组合,有利于免疫细胞毒性和 B 细胞生成和归巢的恢复,提示免疫监测得到改善。