Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Front Immunol. 2022 Sep 2;13:935321. doi: 10.3389/fimmu.2022.935321. eCollection 2022.
In this article, we will share lessons that patients with gain-of-function defects in Toll-like receptor 8 (TLR8-GOF) can teach us about the interface between bone marrow failure (BMF) disorders and inborn errors of immunity (IEI), subsequently referred to as "Interface Disorders". TLR8-GOF is a relatively young entity (from a discovery standpoint) that-through both similar and dissimilar disease characteristics-can increase our understanding of interface disorders, for example, as it pertains to pathophysiology, the genetic mechanism of disease, and related diagnostics and therapeutics. From a genetics point of view, TLR8-GOF joins a growing list of (interface) disorders that can cause disease both with germline and somatic (mosaic) genetic variants. This not only has repercussions for the diagnostic workup of these disorders, inasmuch that routine genetic testing may miss somatic variants, but has therapeutic implications as well, for example, with the approach to curative treatment, such as hematopoietic stem cell transplantation. Following an introduction and schematic rendering of the interface, we will review the salient features of TLR8-GOF, with the understanding that the phenotype of this new disorder is likely not written in stone yet. In keeping with the principle of "Form Follows Function", we will discuss specific immunological biomarkers that can be measured in clinical laboratories and highlight key disease features that pertain to TLR8-GOF, and can be found in several interface disorders. As can be seen from a schematic representation, the interface provides not only opportunities for learning and collaboration with respect to shared diagnostics but also the potential for drug repurposing and precision therapeutics. Ideally, collaboration also focuses on education and teaching, such that cross-fertilization and collaboration across these disciplines can create a framework for complementary research.
在本文中,我们将分享 Toll 样受体 8(TLR8-GOF)功能获得性缺陷患者可以教给我们的关于骨髓衰竭(BMF)疾病和先天性免疫缺陷(IEI)之间界面的经验,此后将其称为“界面疾病”。TLR8-GOF 是一个相对较新的实体(从发现的角度来看),通过相似和不同的疾病特征,可以增加我们对界面疾病的理解,例如,就发病机制、疾病的遗传机制以及相关诊断和治疗而言。从遗传学的角度来看,TLR8-GOF 加入了一系列(界面)疾病,这些疾病既可以由种系遗传变异,也可以由体细胞(嵌合体)遗传变异引起疾病。这不仅对这些疾病的诊断有影响,因为常规基因检测可能会遗漏体细胞变异,而且还会对治疗产生影响,例如,在造血干细胞移植等根治性治疗方法上。在介绍和界面示意图之后,我们将回顾 TLR8-GOF 的显著特征,我们理解这种新疾病的表型可能尚未确定。根据“形式服从功能”的原则,我们将讨论可以在临床实验室中测量的特定免疫学生物标志物,并强调与 TLR8-GOF 相关的关键疾病特征,这些特征在几种界面疾病中都可以找到。从示意图中可以看出,界面不仅为共享诊断提供了学习和合作的机会,而且还为药物再利用和精准治疗提供了潜力。理想情况下,合作还侧重于教育和教学,以便这些学科之间的交叉授粉和合作可以为互补研究创造框架。