Immunopathogenic mechanisms and modulatory approaches to graft-versus-host disease prevention in acute myeloid leukaemia

IF 2.2 4区 医学 Q3 HEMATOLOGY
Yifan Pang , Noa G. Holtzman
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引用次数: 0

Abstract

Allogeneic haematopoietic stem cell transplantation (HSCT) remains the only potential cure for intermediate to high-risk acute myeloid leukaemia (AML). The therapeutic effect of HSCT is largely dependent on the powerful donor-derived immune response against recipient leukaemia cells, known as graft-versus-leukaemia effect (GvL). However, the donor-derived immune system can also cause acute or chronic damage to normal recipient organs and tissues, in a process known as graft-versus-host disease (GvHD). GvHD is a leading cause of non-relapse mortality in HSCT recipients. There are many similarities and cross talk between the immune pathways of GvL and GvHD. Studies have demonstrated that both processes require the presence of mismatched alloantigens between the donor and recipient, and activation of immune responses centered around donor T-cells, which can be further modulated by various recipient or donor factors. Dissecting GvL from GvHD to achieve more effective GvHD prevention and enhanced GvL has been the holy grail of HSCT research. In this review, we focused on the key factors that contribute to the immune responses of GvL and GvHD, the effect on GvL with different GvHD prophylactic strategies, and the potential impact of various AML relapse prevention therapy or treatments on GvHD.

急性髓性白血病移植物抗宿主病预防的免疫致病机制和调节途径
异基因造血干细胞移植(HSCT)仍然是中高风险急性髓细胞白血病(AML)的唯一潜在治疗方法。HSCT的治疗效果在很大程度上取决于供体对受体白血病细胞的强大免疫反应,即移植物抗白血病效应(GvL)。然而,供体来源的免疫系统也会对正常受体器官和组织造成急性或慢性损伤,这一过程被称为移植物抗宿主病(GvHD)。GvHD是造血干细胞移植受者非复发性死亡率的主要原因。GvL和GvHD的免疫途径之间有许多相似之处和相互作用。研究表明,这两个过程都需要供体和受体之间存在不匹配的同种抗原,并激活以供体T细胞为中心的免疫反应,这可以通过各种受体或供体因素进一步调节。从GvHD中分离GvL以实现更有效的GvHD预防和增强GvL一直是HSCT研究的圣杯。在这篇综述中,我们重点讨论了导致GvL和GvHD免疫反应的关键因素,不同的GvHD预防策略对GvL的影响,以及各种AML复发预防治疗或治疗对GvHD的潜在影响。
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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Best Practice & Research Clinical Haematology publishes review articles integrating the results from the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors.
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