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Novel immunosuppression compounds and experimental therapies for chronic graft-versus-host disease

机译:慢性移植物抗宿主病的新型免疫抑制化合物和实验疗法

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摘要

Chronic graft-versus-host disease (GVHD) is a severe complication of allogeneic stem cell transplantation, with a substantial impact on the quality of life and survival, still lacking with regard to an optimal therapeutic strategy. Corticosteroids are considered the standard of care for first-line treatment of chronic GVHD, but only a minority of the patients responds to them durably. Management of steroid-refractory chronic GVHD is not well defined. This review surveys novel treatment strategies, such as therapies that expand regulatory T cells, target B cells or target the processes implicated in fibrosis that may allow more effective control of chronic GVHD in the future. Most therapies are based solely on phase II trials or on retrospective analyses with a wide range of overall responses. Large, well-designed prospective studies are eagerly needed to establish better treatments, as well as valid biomarkers to identify the likelihood of the response to a drug in advance.
机译:慢性移植物抗宿主病(GVHD)是同种异体干细胞移植的严重并发症,对生活质量和生存产生重大影响,但仍缺乏最佳治疗策略。皮质类固醇被认为是慢性GVHD一线治疗的护理标准,但是只有少数患者对它们有持久的反应。尚无明确的类固醇难治性慢性GVHD的治疗方法。这篇综述调查了新颖的治疗策略,例如扩大调节性T细胞,靶向B细胞或靶向与纤维化有关的过程的疗法,这些疗法可能在将来更有效地控制慢性GVHD。大多数疗法仅基于II期临床试验或具有广泛总体反应的回顾性分析。迫切需要进行大型,设计良好的前瞻性研究,以建立更好的治疗方法,以及有效的生物标记物,以预先确定对药物反应的可能性。

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