FSGS复发合作:研讨会报告

Debbie S. Gipson, Chia-shi Wang, Eloise Salmon, Rasheed Gbadegesin, Abhijit Naik, Simone Sanna-Cherchi, Alessia Fornoni, Matthias Kretzler, Sandra Merscher, Paul Hoover, Kelley Kidwell, Moin Saleem, Leonardo Riella, Lawrence Holzman, Annette Jackson, Opeyemi Olabisi, Paolo Cravedi, Benjamin Solomon Freedman, Jonathan Himmelfarb, Marina Vivarelli, Jennifer Harder, Jon Klein, George Burke, Michelle Rheault, Cathie Spino, Hailey E. Desmond, Howard Trachtman
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引用次数: 0

摘要

自50多年前首次被描述以来,同种异体肾脏移植中FSGS的复发一直令移植界感到沮丧。这种罕见的情况与相当高的发病率相关,并且是由于FSGS导致CKD 5期患者移植物丢失的最常见原因。然而,这个问题仍然没有得到充分的研究。这是一种罕见的疾病,个别中心的发病率通常很低,而且难以预测。已发表的文献在基本流行病学数据中包含相互矛盾的报告。在确定疾病机制和推进治疗方案方面的进展有限。目前可用的治疗方案有限,而且大多无效。复发的时间范围和对治疗反应的可变性表明,复发不是一个单一的实体,而是由不同的发病机制引起的多种表型,在一个更大的保护伞下。迫切需要创新的基础科学和转化研究[1],以便从机制角度更好地理解FSGS复发;[2]改善风险分层以预测这一结果;并[3]开发有效的治疗方法。在这份会议报告中,我们描述了研究人员的工作,他们最先进的研究为诊断和治疗问题的创新方法铺平了道路,并为受影响的患者实现这些目标提供了希望。
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FSGS Recurrence Collaboration: Report of a symposium
Since it was first described more than 50 years ago, recurrence of FSGS in kidney allografts has frustrated the transplant community. This rare condition is associated with considerable morbidity, and it is the most common cause of graft loss in patients with CKD stage 5 due to FSGS. However, the problem remains insufficiently studied. It is an ultra-orphan disease and incidence rates at individual centers are often very low and unpredictable. The published literature contains conflicting reports in basic epidemiologic data. Progress in defining the mechanisms of disease and advancing therapeutic options has been limited. The treatment options that are currently available are limited and largely ineffective. The range in time to recurrence and variability in responsiveness to treatment suggest that recurrence is not a single entity, but rather multiple phenotypes resulting from diverse pathogenetic mechanisms grouped under a larger umbrella. There is an urgent need for innovative basic science and translational research to [1] better understand FSGS recurrence from a mechanistic perspective; [2] improve risk stratification to predict this outcome; and [3] develop effective therapies. In this conference report, we describe the work of investigators whose state-of-the-art research paves the way for innovative approaches to diagnosis and treatment of the problem and provides hope that we can achieve these objectives for affected patients.
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