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首页> 外文期刊>Cytotherapy >Improving immune reconstitution while preventing GvHD in allogeneic stem cell transplantation
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Improving immune reconstitution while preventing GvHD in allogeneic stem cell transplantation

机译:在异基因干细胞移植中改善免疫重建并预防GvHD

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摘要

Allogeneic hematopoietic stem cell transplantation (HSCT) is the treatment of choice for many hematologic malignancies and inherited disorders of the hematopoietic system. Ex vivo T-cell depletion (TCD) of the graft and post-transplantation immunosuppression efficiently prevents the development of GvHD in no-MHC-identical settings. However, the consequence of these non-specific strategies is a long-lasting immunodeficiency associated with increased incidence of disease relapse, graft rejection and reactivation of viral infections. Donor lymphocyte infusion, which is used for treating leukemic relapse after allogeneic HSCT, can result in severe GvHD. Several strategies are being optimized specifically to inactivate anti-host T cells while preserving anti-leukemic or anti-microbial immunocompetence. Based on the ex vivo or in vivo elimination of anti-host T cells, or on the modulation of their anti-host activity, these approaches, which have been explored extensively in pre-clinical studies and tested in some preliminary clinical trials, are discussed in this paper.
机译:同种异体造血干细胞移植(HSCT)是许多血液系统恶性肿瘤和造血系统遗传性疾病的首选治疗方法。移植物的离体T细胞耗竭(TCD)和移植后免疫抑制有效地阻止了在无MHC的相同环境下GvHD的发展。然而,这些非特异性策略的结果是长期的免疫缺陷,与疾病复发,移植排斥和病毒感染重新激活的发生率增加相关。供体淋巴细胞输注用于治疗同种异体造血干细胞移植术后的白血病复发,可导致严重的GvHD。目前正在优化几种策略,以在保留抗白血病或抗微生物免疫能力的同时灭活抗宿主T细胞。基于离体或体内消除抗宿主T细胞或调节其抗宿主活性的方法,讨论了在临床前研究中已广泛探索并在一些初步临床试验中进行测试的这些方法。在本文中。

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