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目前和新兴的预防移植物抗宿主病策略。

Current and emerging strategies for the prevention of graft-versus-host disease.

机构信息

Blood and Marrow Transplantation Program, University of Michigan, 1500 East Medical Center Drive, 3312 Cancer Center, Ann Arbor, MI 48109-5942, USA.

出版信息

Nat Rev Clin Oncol. 2014 Sep;11(9):536-47. doi: 10.1038/nrclinonc.2014.102. Epub 2014 Jun 24.

DOI:10.1038/nrclinonc.2014.102
PMID:24958183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4151470/
Abstract

Graft-versus-host disease (GVHD) represents the most serious and challenging complication of allogeneic haematopoietic stem-cell transplantation (HSCT). New insights on the role of regulatory T-cells, T cells, and antigen-presenting cells have led to an improved understanding of the pathophysiology of GVHD. However, little progress has been made since the introduction of calcineurin-inhibitor-based regimens in the mid-1980s. Despite standard prophylaxis with these regimens, GVHD still develops in approximately 40-60% of recipients. Thus, there is a need for developing newer approaches to mitigate GVHD, which may facilitate the use of allogeneic HSCT for the treatment of a wider range of haematological cancers. We discuss the rationale, clinical evidence, and outcomes of current (and widely employed) strategies for GVHD prophylaxis, namely calcineurin-inhibitor-based regimens (such as cyclosporine or tacrolimus) combined with methotrexate or mycophenolate mofetil. We assess the clinical evidence for emerging approaches in the prevention of GVHD, including therapies targeting T cells or B cells, the use of mesenchymal stem cells, chemo-cytokine antagonists (such as maraviroc, TNF-α inhibitor, IL-2 receptor antagonist, IL-6 inhibitor), and the use of novel molecular regulators that target multiple cell types simultaneously, including atorvastatin, bortezomib, and epigenetic modulators.

摘要

移植物抗宿主病(GVHD)是异基因造血干细胞移植(HSCT)最严重和最具挑战性的并发症。对调节性 T 细胞、T 细胞和抗原呈递细胞作用的新认识,导致对 GVHD 病理生理学的理解有所提高。然而,自 20 世纪 80 年代中期引入钙调神经磷酸酶抑制剂为基础的方案以来,几乎没有取得任何进展。尽管采用这些方案进行标准预防,但仍有约 40-60%的受者发生 GVHD。因此,需要开发新的方法来减轻 GVHD,这可能有助于将异基因 HSCT 用于治疗更广泛的血液系统癌症。我们讨论了当前(广泛应用的)GVHD 预防策略的原理、临床证据和结果,即钙调神经磷酸酶抑制剂为基础的方案(如环孢素或他克莫司)联合甲氨蝶呤或霉酚酸酯。我们评估了靶向 T 细胞或 B 细胞的疗法、间充质干细胞的应用、化学细胞因子拮抗剂(如马拉维若、TNF-α 抑制剂、IL-2 受体拮抗剂、IL-6 抑制剂)以及新型分子调节剂(如阿托伐他汀、硼替佐米和表观遗传调节剂)预防 GVHD 的临床证据。

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