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用于多发性骨髓瘤的供体淋巴细胞输注:临床结果与新观点

Donor lymphocyte infusions for multiple myeloma: clinical results and novel perspectives.

作者信息

Zeiser R, Bertz H, Spyridonidis A, Houet L, Finke J

机构信息

Department of Hematology and Oncology, Albert Ludwigs University Medical Center Freiburg, Freiburg, Germany.

出版信息

Bone Marrow Transplant. 2004 Dec;34(11):923-8. doi: 10.1038/sj.bmt.1704670.

Abstract

Donor lymphocyte infusions (DLIs) provide effective therapy for patients with various hematological malignancies who have relapsed after allogeneic hematopoietic stem cell transplantation (HSCT). In patients with multiple myeloma (MM), DLIs can induce response rates of 40-52%. DLIs were employed as treatment for MM relapse or as prophylaxis for relapse in MM patients undergoing allo-HSCT. The clinically most relevant treatment-related morbidity with DLIs is the occurrence of graft-versus-host disease (GVHD). Secondly, graft failure and the immune escape of extramedullary plasmocytoma have been reported. The fact that previous clinical reports have documented graft-versus-myeloma (GVM) activity without GVHD suggests that at least two distinct immunocompetent cell populations mediating GVHD and/or GVM may exist. Further characterization of the effector cells such as T cells and/or NK cells and their targets may help to clarify the immune response that mediates the GVM effect. This review considers the results of clinical approaches with DLI for MM, with emphasis on strategies to prevent GVHD while preserving the GVM effect. Furthermore, currently investigated molecular antigenic targets for the GVM effect such as MM-specific idiotypic determinant of immunoglobulin variable regions, several PRAME epitopes and antigenic structures encoded by cancer germline-specific genes as candidates for immunotherapy trials are discussed.

摘要

供体淋巴细胞输注(DLI)为异基因造血干细胞移植(HSCT)后复发的各种血液系统恶性肿瘤患者提供了有效的治疗方法。在多发性骨髓瘤(MM)患者中,DLI可诱导40%-52%的缓解率。DLI被用于治疗MM复发或作为接受异基因HSCT的MM患者复发的预防措施。DLI临床上最相关的治疗相关发病率是移植物抗宿主病(GVHD)的发生。其次,有报道称存在移植物失败和髓外浆细胞瘤的免疫逃逸。先前的临床报告记录了无GVHD的移植物抗骨髓瘤(GVM)活性,这一事实表明可能存在至少两种介导GVHD和/或GVM的不同免疫活性细胞群。对效应细胞如T细胞和/或NK细胞及其靶标的进一步表征可能有助于阐明介导GVM效应的免疫反应。本综述考虑了DLI治疗MM的临床方法的结果,重点是在保留GVM效应的同时预防GVHD的策略。此外,还讨论了目前正在研究的GVM效应的分子抗原靶点,如免疫球蛋白可变区的MM特异性独特型决定簇、几个PRAME表位以及癌胚特异性基因编码的抗原结构,作为免疫治疗试验的候选靶点。

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