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Hematopoietic Stem Cell Transplantation—50 Years of Evolution and Future Perspectives

机译:造血干细胞移植— 50年的发展和未来展望

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摘要

Hematopoietic stem cell transplantation is a highly specialized and unique medical procedure. Autologous transplantation allows the administration of high-dose chemotherapy without prolonged bone marrow aplasia. In allogeneic transplantation, donor-derived stem cells provide alloimmunity that enables a graft-versus-tumor effect to eradicate residual disease and prevent relapse. The first allogeneic transplantation was performed by E. Donnall Thomas in 1957. Since then the field has evolved and expanded worldwide. New indications beside acute leukemia and aplastic anemia have been constantly explored and now include congenital disorders of the hematopoietic system, metabolic disorders, and autoimmune disease. The use of matched unrelated donors, umbilical cord blood units, and partially matched related donors has dramatically extended the availability of allogeneic transplantation. Transplant-related mortality has decreased due to improved supportive care, including better strategies to prevent severe infections and with the incorporation of reduced-intensity conditioning protocols that lowered the toxicity and allowed for transplantation in older patients. However, disease relapse and graft-versus-host disease remain the two major causes of mortality with unsatisfactory progress. Intense research aiming to improve adoptive immunotherapy and increase graft-versus-leukemia response while decreasing graft-versus-host response might bring the next breakthrough in allogeneic transplantation. Strategies of graft manipulation, tumor-associated antigen vaccinations, monoclonal antibodies, and adoptive cellular immunotherapy have already proved clinically efficient. In the following years, allogeneic transplantation is likely to become more complex, more individualized, and more efficient.
机译:造血干细胞移植是高度专业化和独特的医学程序。自体移植可以进行大剂量化疗,而无需延长骨髓发育不良。在同种异体移植中,供体来源的干细胞提供同种免疫,使移植物抗肿瘤效应得以根除残留疾病并防止复发。 E. Donnall Thomas在1957年进行了第一次同种异体移植。此后,该领域得到了发展和扩展。除了急性白血病和再生障碍性贫血以外,新的适应症也在不断探索,现在包括造血系统的先天性疾病,代谢性疾病和自身免疫性疾病。匹配的无关供体,脐带血单位和部分匹配的相关供体的使用极大地扩展了同种异体移植的可用性。由于改善了支持治疗,包括更好的预防严重感染的策略以及降低强度的调理方案可以降低毒性并允许在老年患者中进行移植,因此与移植相关的死亡率已经降低。然而,疾病复发和移植物抗宿主病仍然是导致死亡的两个主要原因,并且进展不尽人意。旨在改善过继免疫疗法并增加移植物抗白血病反应,同时降低移植物抗宿主反应的大量研究可能会带来同种异体移植的下一个突破。移植物操纵,肿瘤相关抗原疫苗接种,单克隆抗体和过继细胞免疫疗法的策略已被证明在临床上有效。在接下来的几年中,同种异体移植可能会变得更加复杂,更加个性化和更有效率。

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