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Immune Reconstitution after Haploidentical Donor and Umbilical Cord Blood Allogeneic Hematopoietic Cell Transplantation

机译:Haploidentical供体和脐带血异种造血细胞移植免疫重建

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摘要

Allogeneic hematopoietic cell transplantation (HCT) is the only potentially curative therapy for a variety of hematologic diseases. However, this therapeutic platform is limited by an initial period when patients are profoundly immunocompromised. There is gradual immune recovery over time, that varies by transplant platform. Here, we review immune reconstitution after allogeneic HCT with a specific focus on two alternative donor platforms that have dramatically improved access to allogeneic HCT for patients who lack an HLA-matched related or unrelated donor: haploidentical and umbilical cord blood HCT. Despite challenges, interventions are available to mitigate the risks during the immunocompromised period including antimicrobial prophylaxis, modified immune suppression strategies, graft manipulation, and emerging adoptive cell therapies. Such interventions can improve the potential for long-term overall survival after allogeneic HCT.
机译:同种异体造血细胞移植(HCT)是各种血液学疾病的唯一潜在的治疗疗法。然而,这种治疗平台受到患者的初始时期的限制,患者可能是深受免疫造成的。随着时间的推移,存在逐渐免疫恢复,这因移植平台而变化。在这里,我们在同种异体HCT后,对两种替代供体平台的特定重点进行了两项替代的免疫重建,这对缺乏HLA匹配相关或无关的供体的患者进行了显着改善对同种异体HCT的患者:HAPLoIdentical和脐带血HCT。尽管存在挑战,但干预措施可用于减轻免疫激素施用期间的风险,包括抗微生物预防,修饰的免疫抑制策略,接枝操纵和新出现的养殖细胞疗法。这种干预措施可以改善同种异体HCT后长期整体存活的潜力。

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