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急性淋巴细胞白血病的细胞疗法

Cellular therapies in acute lymphoblastic leukemia.

作者信息

Brentjens Renier J

机构信息

Memorial Sloan Kettering Cancer Center, Department of Medicine, Leukemia Service, New York, NY 10065, USA.

出版信息

Curr Opin Mol Ther. 2009 Aug;11(4):375-82.

Abstract

The majority of adult patients with acute lymphoblastic leukemia (ALL) will die from the disease. Although the prognosis for pediatric patients is significantly better than for adult patients with ALL, the prognosis for patients with relapsed or refractory disease is poor in all cases. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) from a related donor offers a significant therapeutic benefit for pediatric patients, although the benefit of this therapy to adults with ALL is less established. Because most patients lack a suitable related donor, alternative approaches to allo-HSCT, including umbilical cord blood, and unrelated and haploidentical allo-HSCT, have been investigated in the clinical setting. Although treatment with donor-derived T-cells, so-called 'donor lymphocyte infusion', has demonstrated poor outcomes in patients with relapsed ALL following HSCT, modified adoptive T-cell regimens, including the infusion of enriched tumor-targeted donor T-cells and genetically targeted T-cells, are currently under clinical investigation. In addition, the resistance of ALL tumor cell lines to NK-cell-mediated lysis may be overcome by the genetic modification of NK cells to target ALL tumor cell antigens, and this approach will be evaluated in an upcoming clinical trial. Whether these novel adoptive cell therapies will ultimately result in improved clinical outcomes remains to be determined.

摘要

大多数成年急性淋巴细胞白血病(ALL)患者会死于该疾病。尽管儿科患者的预后明显优于成年ALL患者,但复发或难治性疾病患者的预后在所有情况下都很差。来自相关供体的异基因造血干细胞移植(allo-HSCT)对儿科患者具有显著的治疗益处,尽管这种疗法对成年ALL患者的益处尚不明确。由于大多数患者缺乏合适的相关供体,因此在临床环境中对allo-HSCT的替代方法进行了研究,包括脐带血、无关供体和单倍体相合allo-HSCT。尽管供体来源的T细胞治疗(即所谓的“供体淋巴细胞输注”)在HSCT后复发的ALL患者中显示出较差的结果,但目前正在对改良的过继性T细胞方案进行临床研究,包括输注富集的肿瘤靶向供体T细胞和基因靶向T细胞。此外,通过对NK细胞进行基因改造以靶向ALL肿瘤细胞抗原,可能会克服ALL肿瘤细胞系对NK细胞介导的裂解的抗性,并且这种方法将在即将进行的临床试验中进行评估。这些新型过继性细胞疗法最终是否会改善临床结果仍有待确定。

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