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Neutrophil Extracellular Traps (NETs): An unexplored territory in renal pathobiology, a pilot computational study

机译:中性粒细胞外细胞疏水阀(网):肾病学的未开发领土,试点计算研究

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In the age of modern medicine and artificial intelligence, image analysis and machine learning have revolutionizeddiagnostic pathology, facilitating the development of computer aided diagnostics (CADs) which circumvent prevalentdiagnostic challenges. Although CADs will expedite and improve the precision of clinical workflow, their prognosticpotential, when paired with clinical outcome data, remains indeterminate. In high impact renal diseases, such asdiabetic nephropathy and lupus nephritis (LN), progression often occurs rapidly and without immediate detection, dueto the subtlety of structural changes in transient disease states. In such states, exploration of quantifiable imagebiomarkers, such as Neutrophil Extracellular Traps (NETs), may reveal alternative progression measures whichcorrelate with clinical data. NETs have been implicated in LN as immunogenic cellular structures, whose occurrenceand dysregulation results in excessive tissue damage and lesion manifestation. We propose that renal biopsy NETdistribution will function as a discriminate, predictive biomarker in LN, and will supplement existing classificationschemes. We have developed a computational pipeline for segmenting NET-like structures in LN biopsies. NET-likestructures segmented from our biopsies warrant further study as they appear pathologically distinct, and resemble nonlytic,vital NETs. Examination of corresponding H&E regions predominantly placed NET-like structures in glomeruli,including globally and segmentally sclerosed glomeruli, and tubule lumina. Our work continues to explore NET-likestructures in LN biopsies by: 1.) revising detection and analytical methods based on evolving NETs definitions, and2.) cataloguing NET morphology in order to implement supervised classification of NET-like structures inhistopathology images.
机译:在现代医学和人工智能的时代,图像分析和机器学习已经彻底改变了诊断病理学,促进计算机辅助诊断(CADS)的发展,这是普遍存在的诊断挑战。虽然CADS将加快并提高临床工作流程的精度,但其预后当与临床结果数据配对时,潜力仍然不确定。在高抗冲肾疾病中,如糖尿病肾病和狼疮肾炎(LN),往往会迅速发生,而无需立即检测,到期瞬态疾病状态结构变化的细节。在这些状态下,探索量化图像诸如中性粒细胞面细胞疏水阀(网)的生物标志物可以揭示替代进展措施与临床数据相关。网的蚊帐是免疫原性细胞结构的含义,其发生并且失调导致组织损伤过度和病变表现。我们提出肾活检网分布将作为LN中的区分,预测生物标志物起作用,并将补充现有的分类方案。我们开发了一种用于在LN活组织检查中分割网状结构的计算管道。网从我们的活组织检查分割的结构需要进一步研究,因为它们显得明显,并且类似于非赖赖特,重要网。检查相应的H&E区域主要放置在Glomeruli中的网状结构,包括全球和分段型硬化的肾小球和小管菌丝。我们的工作继续探索网状LN活组织检查中的结构通过:1。)根据不断发展的网络定义进行修改检测和分析方法2.)目录净形态,以实施网络状结构的监督分类组织病理学图像。

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