首页> 外文期刊>Bone marrow transplantation >Long term disease-free survival in acute leukemia patients recovering with increased gammadelta T cells after partially mismatched related donor bone marrow transplantation.
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Long term disease-free survival in acute leukemia patients recovering with increased gammadelta T cells after partially mismatched related donor bone marrow transplantation.

机译:急性白血病患者的长期无病生存率是在部分不匹配的相关供体骨髓移植后因γ-T细胞增加而恢复。

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Allogeneic stem cell transplantation (ASCT) has improved leukemia-free survival (LFS) in many but not all patients with acute leukemia. This is an eight-year follow-up to our previous study showing a survival advantage to patients with an increased gammadelta T cells following ASCT. gammadelta T cell levels were collected prospectively in 153 patients (acute lymphoblastic leukemia (ALL) n = 77; acute myelogenous leukemia (AML) n = 76) undergoing partially mismatched related donor ASCT. Median age was 22 years (1-59), and 62% of the patients were in relapse at transplant. Patient-donor human leukocyte antigen (HLA) disparity of three antigens was 37% in the graft-versus-host disease (GvHD) and 29% in the rejection directions. All patients received a partially T cell-depleted graft using T10B9 (n = 46) or OKT3 (n = 107). Five years LFS and overall survival (OS) of patients with increased gammadelta compared to those with normal/decreased numbers were 54.4 vs 19.1%; P < 0.0003, and 70.8 vs 19.6% P < 0.0001, respectively, with no difference in GvHD (P = 0.96). In a Cox multivariate analysis, normal/decreased gammadelta (hazard ratio (HR) 4.26, P = 0.0002) and sex mismatch (HR 1.45 P=0.049) were associated with inferior LFS. In conclusion, gammadelta T cells may facilitate a graft-versus-leukemia (GvL) effect, without causing GvHD. Further evaluations of this effect may lead to specific immunotherapy for patients with refractory leukemia.
机译:同种异体干细胞移植(ASCT)在许多但并非所有急性白血病患者中均改善了无白血病生存期(LFS)。这是对我们先前研究的八年跟踪研究,显示了ASCT后具有增加的Gammadelta T细胞的患者的生存优势。前瞻性收集了153例接受部分不匹配的相关供体ASCT的患者(急性淋巴细胞白血病(ALL)n = 77;急性骨髓性白血病(AML)n = 76)中的γT细胞水平。中位年龄为22岁(1-59),其中62%的患者在移植时复发。在移植物抗宿主病(GvHD)中,三种抗原的患者-供体人类白细胞抗原(HLA)差异为37%,在排斥方向上为29%。所有患者均使用T10B9(n = 46)或OKT3(n = 107)接受了部分T细胞缺失的移植物。与正常/下降人数相比,伽玛三角洲增加的患者的五年LFS和总生存(OS)分别为54.4和19.1%; P <0.0003,分别为70.8和19.6%P <0.0001,而GvHD无差异(P = 0.96)。在Cox多变量分析中,正常/降低的伽玛三角洲(危险比(HR)4.26,P = 0.0002)和性别不匹配(HR 1.45 P = 0.049)与低位LFS相关。总之,γT细胞可能促进移植物抗白血病(GvL)效应,而不会引起GvHD。对该效果的进一步评估可能会导致难治性白血病患者进行特异性免疫治疗。

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