人类胰腺在1型糖尿病进展阶段的综合组织病理学。

Dirk Homann, Verena van der Heide, Sara McArdle, Michael Nelson, Karen Cerosaletti, Sacha Gnjatic, Zbigniew Mikulski, Amanda Posgai, Irina Kusmartseva, Mark Atkinson
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引用次数: 0

摘要

1型糖尿病(T1D)是一种进行性自身免疫性疾病,最终导致产生胰岛素的β细胞的损失。胰腺组织病理学为疾病的发生和进展提供了必要的见解,但缺乏对原位致病过程的综合观点。在这里,我们结合了多重免疫染色、高倍全切片成像、数字病理学和半自动图像分析,对T1D分期的胰腺尾部和头部切片进行了研究,包括高危和发病病例。对约25,000个胰岛的结构特征、内分泌细胞组成、免疫细胞负荷和空间关系进行反卷积,有效地将健康和T1D疾病中已建立的和新的胰腺特征置于背景下。我们的研究结果揭示了内分泌胰腺的空间同质和胰岛大小偶然的建筑组织,全器官致病过程的显着协调,以及多种组织病理学相关性,预示着已经在临床前阶段的独特T1D组织病理学。总之,我们提出了一个修订的T1D的自然史,对进一步的组织病理学调查和病理模式的考虑的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated histopathology of the human pancreas throughout stages of type 1 diabetes progression.

Type 1 diabetes (T1D) is a progressive autoimmune condition that culminates in loss of insulin-producing beta cells. Pancreatic histopathology provides essential insights into disease initiation and progression yet an integrated perspective onto in situ pathogenic processes is lacking. Here, we combined multiplexed immunostaining, high-magnification whole-slide imaging, digital pathology, and semi-automated image analyses to interrogate pancreatic tail and head sections across T1D stages, including at-risk and at-onset cases. Deconvolution of architectural features, endocrine cell composition, immune cell burden, and spatial relations of ~ 25,000 islets effectively contextualizes established and novel pancreatic hallmarks in health and T1D disease. Our results reveal a spatially homogenous and islet size-contingent architectural organization of the endocrine pancreas, a notable coordination of organ-wide pathogenic processes, and multiple histopathological correlates that foreshadow distinctive T1D histopathology already at the preclinical stage. Altogether, we propose a revised natural history of T1D with implications for further histopathological investigations and considerations of pathogenetic modalities.

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