Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Biol Blood Marrow Transplant. 2011 Mar;17(3):374-83. doi: 10.1016/j.bbmt.2010.07.003. Epub 2010 Jul 15.
Donor lymphocyte infusions (DLIs) are used for adoptive immunotherapy to prevent or treat relapse and infectious complications after allogeneic hematopoietic stem cell transplantation (HSCT). Unmanipulated DLIs are associated with a risk of graft-versus-host disease (GVHD), probably related to CD8(+) T cell activity. We investigated an automated clinical-scale human-CD4(+)-cell purification method to deplete CD8(+) cells. Twenty-four stem cell recipients received a total of 24 leukapheresis products being enriched for CD4(+) cells using magnetic associated cell sorting (MACS) with an automated device (CliniMACS(®)) before DLIs. MACS resulted in a mean CD4(+) cell count of 16 × 10(6)/kg bw corresponding to 3.4-fold CD4(+) cell enrichment. Mean yield and purity of CD45(+)CD3(+)CD4(+)CD14(-)7AAD(-) were 74% ± 23% and 82% ± 11%, respectively. Median initial dose of DLIs was 1.1 × 10(6) CD4(+)/kg. During a median follow-up of 25 months, 7 (30%) patients experienced GVHD (acute II-IV: n = 4, 17%; acute III-IV: n = 2, 8%; chronic limited: n = 2, 8%; chronic extensive: n = 1, 4%). Thirteen of 21 further evaluable patients (62%) showed measurable clinical response, 2 patients with therapy refractory infectious complications (HSV) showed remarkable immunologic improvement. Automated enrichment of CD4(+) by magnetic cell sorting provides an efficient and rapid method for processing donor lymphocytes. Additional studies should further investigate this approach in terms of efficacy and the risk of GVHD.
供者淋巴细胞输注(DLI)用于过继免疫治疗,以预防或治疗异基因造血干细胞移植(HSCT)后的复发和感染并发症。未处理的 DLI 与移植物抗宿主病(GVHD)的风险相关,可能与 CD8+T 细胞活性有关。我们研究了一种自动化的临床规模的人 CD4+细胞纯化方法,以去除 CD8+细胞。24 名干细胞受者共接受了 24 次白细胞分离术产物,在输注 DLI 之前,使用磁性相关细胞分选(MACS)和自动化设备(CliniMACS®)对其进行 CD4+细胞富集。MACS 导致 CD4+细胞计数的平均值为 16×106/kg bw,对应于 CD4+细胞的 3.4 倍富集。CD45+CD3+CD4+CD14-CD7AAD-的平均产量和纯度分别为 74%±23%和 82%±11%。DLI 的初始剂量中位数为 1.1×106 CD4+/kg。在中位数为 25 个月的随访期间,7(30%)名患者发生 GVHD(急性 II-IV:n=4,17%;急性 III-IV:n=2,8%;慢性局限性:n=2,8%;慢性广泛性:n=1,4%)。21 名可进一步评估的患者中有 13 名(62%)出现可测量的临床反应,2 名因治疗难治性感染并发症(HSV)的患者出现明显的免疫改善。通过磁性细胞分选自动富集 CD4+提供了一种高效快速的方法来处理供者淋巴细胞。进一步的研究应该进一步探讨这种方法在疗效和 GVHD 风险方面的应用。