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采用来自具有一个完全错配HLA单倍型的相关供体的T细胞去除干细胞治疗高危急性白血病。

Treatment of high-risk acute leukemia with T-cell-depleted stem cells from related donors with one fully mismatched HLA haplotype.

作者信息

Aversa F, Tabilio A, Velardi A, Cunningham I, Terenzi A, Falzetti F, Ruggeri L, Barbabietola G, Aristei C, Latini P, Reisner Y, Martelli M F

机构信息

Department of Internal and Experimental Medicine, University of Perugia, Italy.

出版信息

N Engl J Med. 1998 Oct 22;339(17):1186-93. doi: 10.1056/NEJM199810223391702.

Abstract

BACKGROUND

In this study we tried to achieve successful transplantation in patients with acute leukemia with the use of hematopoietic stem cells from donors who shared only one HLA haplotype with the recipient (a "full-haplotype mismatch"). To prevent graft failure, large doses of T-cell-depleted hematopoietic stem cells were transplanted after a conditioning regimen of enhanced myeloablation and immunosuppression was administered to the recipient.

METHODS

Forty-three patients with high-risk acute leukemia who were scheduled for transplantation received total-body irradiation, thiotepa, fludarabine, and antithymocyte globulin. The graft consisted of peripheral-blood progenitor cells that had been mobilized in the donor with recombinant granulocyte colony-stimulating factor and also, in 28 cases, bone marrow. Bone marrow from the donor was depleted of T lymphocytes by processing with soybean agglutinin and E-rosetting. T-cell depletion of peripheral-blood mononuclear cells was achieved by E-rosetting followed by positive selection of CD34+ cells. No post-transplantation prophylaxis against graft-versus-host disease (GVHD) was administered.

RESULTS

In all the patients, full donor-type engraftment was achieved. In none of the patients who could be evaluated did acute or chronic GVHD develop. Regimen-related toxicity was minimal. Eleven of the 23 patients with acute lymphoblastic leukemia had a relapse, as did 2 of the 20 patients with acute myeloid leukemia. Transplantation-related mortality was 40 percent. After a median follow-up of 18 months (range, 8 to 30), 12 of the 43 patients were alive and free of disease. All surviving patients had a good quality of life.

CONCLUSIONS

The main limitations of transplantation of bone marrow from donors who are matched with the recipient for only one HLA haplotype GVHD and graft failure - can be overcome. Since most patients have a relative with one haplotype mismatch, advances in this method will increase the availability of hematopoietic-cell transplantation as curative therapy for acute leukemia.

摘要

背景

在本研究中,我们尝试利用与受者仅共享一个HLA单倍型(“完全单倍型错配”)的供者的造血干细胞,在急性白血病患者中实现成功移植。为防止移植失败,在对受者进行强化骨髓清除和免疫抑制预处理方案后,移植大剂量去除T细胞的造血干细胞。

方法

43例计划进行移植的高危急性白血病患者接受了全身照射、噻替派、氟达拉滨和抗胸腺细胞球蛋白治疗。移植物包括用重组粒细胞集落刺激因子动员供者的外周血祖细胞,28例还包括骨髓。供者骨髓经大豆凝集素和E花环处理去除T淋巴细胞。外周血单个核细胞通过E花环然后阳性选择CD34+细胞实现T细胞清除。未进行移植后移植物抗宿主病(GVHD)预防。

结果

所有患者均实现完全供者型植入。在所有可评估的患者中均未发生急性或慢性GVHD。方案相关毒性最小。23例急性淋巴细胞白血病患者中有11例复发,20例急性髓细胞白血病患者中有2例复发。移植相关死亡率为40%。中位随访18个月(范围8至30个月)后,43例患者中有12例存活且无疾病。所有存活患者生活质量良好。

结论

仅与受者匹配一个HLA单倍型的供者骨髓移植的主要局限性——GVHD和移植失败——可以克服。由于大多数患者有一个单倍型错配的亲属,该方法的进展将增加造血细胞移植作为急性白血病治愈性治疗的可及性。

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