同种异体干细胞移植的研究进展:移植物对抗白血病治疗实体瘤

R. Childs, R. Srinivasan
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引用次数: 36

摘要

同种异体干细胞移植最初是作为高剂量“清髓”治疗血液系统恶性肿瘤后恢复造血功能的一种方法而发展起来的。在最初的20年里,剂量强化化疗被认为可以治愈那些在此过程中获得持续缓解的患者。然而,最近研究人员已经认识到,通过移植同种异体干细胞的免疫能力供体t细胞介导的抗肿瘤作用可以诱导对抗血液系统恶性肿瘤。事实上,这种移植物抗白血病(GVL)或移植物抗肿瘤(GVT)效应现在被认为是维持这种方法后血液系统恶性肿瘤持久缓解所需的主要模式。GVT在血液学癌症中的强大和潜在的治疗性质最近吸引了肿瘤学家探索异体干细胞移植作为治疗难治性实体肿瘤的研究方法的治疗潜力。我们在此回顾异体干细胞移植作为潜在的实体瘤免疫疗法的发展和早期临床结果。
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Advances in Allogeneic Stem Cell Transplantation: Directing Graft‐Versus‐Leukemia at Solid Tumors
Allogeneic stem cell transplantation was originally developed as a method to rescue hematopoietic function following high dose “myeloablative” therapy in the treatment of hematological malignancies. In the first two decades of its use, dose-intensive chemotherapy alone was credited with curing those patients who achieved sustained remission following this procedure. However, more recently investigators have come to recognize that antineoplastic effects mediated by immunocompetent donor T-cells transplanted with the stem cell allograft can be induced against hematological malignancies. Indeed, this graft-vs-leukemia (GVL) or graft-vs-tumor (GVT) effect is now felt to represent the principal modality required to sustain durable remissions of hematological malignancies following this approach. The powerful and potentially curative nature of the GVT effect in hematological cancers has recently lured oncologists into exploring the therapeutic potential of allogeneic stem cell transplantation as an investigational approach for treatment-refractory solid tumors. We review here the development and early clinical results of allogeneic stem cell transplantation as potential immunotherapy for solid tumors.
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