Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, Minnesota, USA.
Biol Blood Marrow Transplant. 2010 May;16(5):565-86. doi: 10.1016/j.bbmt.2010.02.005. Epub 2010 Feb 10.
The success of allogeneic hematopoietic stem cell transplantation (HSCT) depends on the infusion of benign stem cells as well as lymphocytes capable of participating in a graft-versus-tumor/leukemia (GVL) reaction. Clinical proof of concept is derived from studies showing increased relapse after the infusion of lymphocyte depleted hematopoietic grafts as well as the therapeutic efficacy of donor lymphocyte infusions without chemotherapy to treat relapse in some diseases. Despite this knowledge, relapse after allogeneic HSCT is common with rates approaching 40% in those with high-risk disease. In this review, we cover the basic biology and potential application to exploit adaptive T cell responses, minor histocompatibility antigens, contraction and suppression mechanisms that hinder immune responses, adaptive B cell responses and innate NK cell responses, all orchestrated in a GVL reaction. Optimal strategies to precisely balance immune responses to favor GVL without harmful graft-versus-host disease (GVHD) are needed to protect against relapse, treat persistent disease and improve disease-free survival after HSCT.
异基因造血干细胞移植(HSCT)的成功依赖于输注良性干细胞以及能够参与移植物抗宿主病/白血病(GVL)反应的淋巴细胞。临床概念验证源自于研究表明,输注淋巴细胞耗竭的造血移植物后复发率增加,以及在某些疾病中无需化疗即可通过供者淋巴细胞输注治疗复发的治疗效果。尽管有这些认识,但异基因 HSCT 后仍会发生复发,高危疾病患者的复发率接近 40%。在这篇综述中,我们涵盖了基础生物学和潜在应用,以利用适应性 T 细胞反应、次要组织相容性抗原、限制免疫反应的收缩和抑制机制、适应性 B 细胞反应和先天 NK 细胞反应,所有这些都在 GVL 反应中进行协调。需要制定最佳策略来精确平衡免疫反应,以有利于 GVL 而不产生有害的移植物抗宿主病(GVHD),从而防止复发、治疗持续性疾病并改善 HSCT 后的无病生存。