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高危急性白血病替代供者造血干细胞移植:单倍体相合供者选择

Hematopoietic stem cell transplantation from alternative donors for high-risk acute leukemia: the haploidentical option.

作者信息

Aversa Franco, Tabilio Antonio, Velardi Andrea, Terenzi Adelmo, Falzetti Franca, Carotti Alessandra, Aloisi Teresa, Liga Maria, Di Ianni Mauro, Zei Tiziana, Santucci Antonella, Martelli Massimo F

机构信息

Hematopoietic Stem Cell Transplant Unit, Section of Hematology and Immunology, Department of Clinical and Experimental Medicine, University of Perugia, Perugia 06100, Italy.

出版信息

Curr Stem Cell Res Ther. 2007 Jan;2(1):105-12. doi: 10.2174/157488807779316973.

Abstract

Much progress has been made in the clinical, biological and technical aspects of the T-cell-depleted full-haplotype mismatched transplants for acute leukemia. Our experience demonstrates that infusing a megadose of extensively T-cell-depleted hematopoietic peripheral blood stem cells after an immuno-myeloablative conditioning regimen in acute leukemia patients ensures sustained engraftment with minimal graft-vs-host disease (GvHD) without the need of any post-transplant immunosuppressive treatment. Since our first successful pilot study, our efforts have concentrated on developing new conditioning regimens, optimizing the graft processing and improving the post-transplant immunological recovery. The results we have so far achieved in more than 200 high-risk acute leukemia patients show that haploidentical transplantation is now a clinical reality. Because virtually all patients in need of a hematopoietic stem cell transplant have a full-haplotype mismatched donor, who is immediately available, a T-cell depleted mismatched transplant should be offered, not as a last resort, but as a viable option to high risk acute leukemia patients who do not have, or cannot find, a matched donor.

摘要

在急性白血病的T细胞去除全单倍型不匹配移植的临床、生物学和技术方面已经取得了很大进展。我们的经验表明,在急性白血病患者接受免疫清髓预处理方案后,输注大剂量的广泛T细胞去除的造血外周血干细胞,可确保持续植入,且移植物抗宿主病(GvHD)最小,无需任何移植后免疫抑制治疗。自我们首次成功的试点研究以来,我们一直致力于开发新的预处理方案、优化移植物处理并改善移植后的免疫恢复。我们迄今在200多名高危急性白血病患者中取得的结果表明,单倍型相合移植现已成为临床现实。由于几乎所有需要造血干细胞移植的患者都有全单倍型不匹配的供体,且该供体可立即获得,因此应向没有或无法找到匹配供体的高危急性白血病患者提供T细胞去除的不匹配移植,这不应作为最后的手段,而应作为一种可行的选择。

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