首页> 外文期刊>Bone marrow transplantation >Donor CD4 T cells convert mixed to full donor T-cell chimerism and replenish the CD52-positive T-cell pool after alemtuzumab-based T-cell-depleted allo-transplantation.
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Donor CD4 T cells convert mixed to full donor T-cell chimerism and replenish the CD52-positive T-cell pool after alemtuzumab-based T-cell-depleted allo-transplantation.

机译:供体CD4 T细胞混合后可完全转化为供体T细胞嵌合体,并在基于阿仑单抗的T细胞贫化同种异体移植后补充CD52阳性T细胞池。

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摘要

Donor lymphocyte infusions (DLI) are used to resolve mixed T-cell chimerism (TCC) after allo-SCT despite a substantial risk of GVHD. We analyzed the impact of prophylactic CD8-depleted (CD8(depl)) DLI in 20 recipients of anti-CD52 alemtuzumab in vivo T-cell-depleted allografts with declining donor TCC after day +60. A total of 13 patients received CD8(depl) DLI and 7 patients did not. All but one of the DLI patients converted to complete donor T-cell chimeras, whereas only one non-DLI patient converted spontaneously. DLI induced transient acute GVHD in five and extensive chronic GVHD in two patients. These data suggest the use of CD8(depl) DLI as an effective treatment for mixed TCC, particularly in patients at high risk for GVHD. We also observed that the majority of reconstituting donor-derived T cells after alemtuzumab conditioning were CD52-negative. CD8(depl) DLI significantly increased the proportion of CD52-positive CD4 T cells, whereby their beneficial effect on reconstituting the post-transplant T-cell repertoire was shown.
机译:尽管有严重的GVHD风险,但在allo-SCT后使用供体淋巴细胞输注(DLI)解决混合的T细胞嵌合体(TCC)。我们分析了预防性的CD8耗竭(CD8(depl))DLI对抗CD52的alemtuzumab体内T细胞耗竭的同种异体移植患者的+20天后第60天TCC下降的影响。共有13例患者接受了CD8(depl)DLI,而7例患者未接受。除一名DLI患者外,所有患者均转化为完整的供体T细胞嵌合体,而只有一名非DLI患者自发转化。 DLI在5例患者中引起短暂的急性GVHD,在2例患者中引起广泛的慢性GVHD。这些数据表明使用CD8(depl)DLI作为混合TCC的有效治疗方法,尤其是在GVHD高危患者中。我们还观察到,Alemtuzumab调节后,大多数重组供体来源的T细胞均为CD52阴性。 CD8(depl)DLI显着增加了CD52阳性CD4 T细胞的比例,从而显示了它们对重建移植后T细胞库的有益作用。

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