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在费城染色体阳性急性淋巴细胞白血病患者中,通过诱导异基因干细胞移植后的移植物抗宿主病来清除残留的bcr-abl阳性克隆。

Eradication of residual bcr-abl-positive clones by inducing graft-versus-host disease after allogeneic stem cell transplantation in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.

作者信息

Matsue K, Tabayashi T, Yamada K, Takeuchi M

机构信息

Division of Hematology/Oncology, Department of Medicine, Kameda General Hospital, Kamogawa, Chiba, Japan.

出版信息

Bone Marrow Transplant. 2002 Jan;29(1):63-6. doi: 10.1038/sj.bmt.1703318.

Abstract

Persistence of bcr-abl transcripts after marrow grafting is thought to convey a high risk for relapse in patients with Philadelphia chromosome (Ph)-positive acute lymphoblastic leukemia (ALL). Donor leukocyte infusion (DLI) is closely associated with development of graft-versus-host disease (GVHD) and has well-defined activity against relapsed chronic myelogenous leukemia (CML) but not ALL. We report two patients with Ph-positive ALL who remained bcr-abl positive by reverse transcriptase polymerase chain reaction (RT-PCR) after marrow grafting. Residual bcr-abl transcripts in both patients were eliminated following acute GVHD, which was induced by either DLI or rapid reduction of immunosuppression. Both patients have continued in complete molecular remission for 18 months and 8 months following transplantation, respectively. Our observation suggests that induction of GVHD may eliminate minimal residual disease, thereby preventing leukemia relapse in patients transplanted for Ph-positive ALL.

摘要

骨髓移植后bcr-abl转录本的持续存在被认为与费城染色体(Ph)阳性急性淋巴细胞白血病(ALL)患者的高复发风险相关。供体白细胞输注(DLI)与移植物抗宿主病(GVHD)的发生密切相关,并且对复发的慢性粒细胞白血病(CML)具有明确的活性,但对ALL无效。我们报告了两名Ph阳性ALL患者,他们在骨髓移植后通过逆转录酶聚合酶链反应(RT-PCR)检测仍为bcr-abl阳性。两名患者残留的bcr-abl转录本在由DLI或快速降低免疫抑制诱导的急性GVHD后均被清除。两名患者分别在移植后18个月和8个月持续处于完全分子缓解状态。我们的观察表明,诱导GVHD可能消除微小残留病,从而预防接受Ph阳性ALL移植患者的白血病复发。

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