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[慢性移植物抗宿主病:诊断与治疗]

[Chronic graft-versus-host disease: diagnosis and treatment].

作者信息

Inamoto Yoshihiro

机构信息

Division of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital.

出版信息

Rinsho Ketsueki. 2018;59(5):549-556. doi: 10.11406/rinketsu.59.549.

Abstract

Chronic graft-versus-host disease (cGVHD) occurs in approximately 40% of patients who undergo allogeneic hematopoietic cell transplantation. It affects various organs and causes significant morbidity and mortality. The manifestations of cGVHD resemble those of autoimmune diseases. Inflammation, cellular immunity, humoral immunity, and fibrosis are implicated in cGVHD pathogenesis. The 2005 NIH consensus criteria for cGVHD have set standards for designing and reporting clinical trials, and the criteria were revised in 2014 to incorporate accumulated evidence and questions. The criteria are ready to be applied to design clinical trials aimed at identifying drugs for the treatment of cGVHD. Recent preclinical cGVHD trials have revealed the central roles of regulatory T cells, Th17 cells, Tc17 cells, follicular helper T cells, and follicular regulatory T cells as well as B cell signaling and fibrosis-promoting factors. Based on these advances, clinical trials targeting the specific pathogenic pathways of cGVHD are rapidly emerging, awaiting the approval of effective drugs to improve patient outcomes.

摘要

慢性移植物抗宿主病(cGVHD)发生于约40%接受异基因造血细胞移植的患者中。它会影响多个器官,并导致显著的发病率和死亡率。cGVHD的表现类似于自身免疫性疾病。炎症、细胞免疫、体液免疫和纤维化都与cGVHD的发病机制有关。2005年美国国立卫生研究院(NIH)关于cGVHD的共识标准为设计和报告临床试验设定了标准,2014年对该标准进行了修订,以纳入积累的证据和问题。这些标准已准备好应用于设计旨在识别治疗cGVHD药物的临床试验。最近的临床前cGVHD试验揭示了调节性T细胞、Th17细胞、Tc17细胞、滤泡辅助性T细胞和滤泡调节性T细胞以及B细胞信号传导和纤维化促进因子的核心作用。基于这些进展,针对cGVHD特定致病途径的临床试验正在迅速涌现,等待有效药物的获批以改善患者预后。

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