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移植物抗白血病活性可能克服免疫球蛋白可变重链基因未突变状态的慢性淋巴细胞白血病的治疗耐药性:定量PCR检测微小残留病的意义

Graft-versus-leukemia activity may overcome therapeutic resistance of chronic lymphocytic leukemia with unmutated immunoglobulin variable heavy-chain gene status: implications of minimal residual disease measurement with quantitative PCR.

作者信息

Ritgen Matthias, Stilgenbauer Stephan, von Neuhoff Nils, Humpe Andreas, Brüggemann Monika, Pott Christiane, Raff Thorsten, Kröber Alexander, Bunjes Donald, Schlenk Richard, Schmitz Norbert, Döhner Hartmut, Kneba Michael, Dreger Peter

机构信息

Second Department of Internal Medicine, Chemnitzstr 33, D-24116 Kiel, Germany.

出版信息

Blood. 2004 Oct 15;104(8):2600-2. doi: 10.1182/blood-2003-12-4321. Epub 2004 Jun 17.

Abstract

The aim of this study was to investigate if graft-versus-leukemia (GVL) activity conferred by allogeneic stem cell transplantation (allo-SCT) is effective in chronic lymphocytic leukemia (CLL) with unmutated V(H) gene status. The kinetics of residual disease (MRD) were measured by quantitative allele-specific immunoglobulin heavy chain (IgH) polymerase chain reaction (PCR) in 9 patients after nonmyeloablative allo-SCT for unmutated CLL. Despite an only modest decrease in the early posttransplantation phase, MRD became undetectable in 7 of 9 patients (78%) from day +100 onwards subsequent to chronic graft-versus-host disease or donor lymphocyte infusions. With a median follow-up of 25 months (range, 14-37 months), these 7 patients remain in continuous clinical and molecular remission. In contrast, PCR negativity was achieved in only 6 of 26 control patients (23%) after autologous SCT for unmutated CLL and it was not durable. Taken together, this study shows for the first time that GVL-mediated immunotherapy might be effective in CLL with unmutated V(H).

摘要

本研究的目的是调查异基因干细胞移植(allo-SCT)赋予的移植物抗白血病(GVL)活性在V(H)基因未突变的慢性淋巴细胞白血病(CLL)中是否有效。通过定量等位基因特异性免疫球蛋白重链(IgH)聚合酶链反应(PCR),对9例接受非清髓性allo-SCT治疗的V(H)基因未突变CLL患者的残留疾病(MRD)动力学进行了测量。尽管在移植后早期仅出现适度下降,但在慢性移植物抗宿主病或供体淋巴细胞输注后的第100天起,9例患者中有7例(78%)的MRD变得无法检测到。中位随访25个月(范围14 - 37个月),这7例患者仍处于持续的临床和分子缓解状态。相比之下,26例接受自体SCT治疗的V(H)基因未突变CLL对照患者中,只有6例(23%)实现了PCR阴性,且这种阴性并不持久。综上所述,本研究首次表明GVL介导的免疫疗法可能对V(H)基因未突变的CLL有效。

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