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1型糖尿病进展各阶段人类胰腺的综合组织病理学研究

Integrated histopathology of the human pancreas throughout stages of type 1 diabetes progression.

作者信息

van der Heide Verena, McArdle Sara, Nelson Michael S, Cerosaletti Karen, Gnjatic Sacha, Mikulski Zbigniew, Posgai Amanda L, Kusmartseva Irina, Atkinson Mark, Homann Dirk

机构信息

Marc and Jennifer Lipschultz Precision Immunology Institute, Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai (ISMMS), New York, NY 10029, USA.

These authors contributed equally.

出版信息

bioRxiv. 2025 Mar 19:2025.03.18.644000. doi: 10.1101/2025.03.18.644000.

Abstract

Type 1 diabetes (T1D) is a progressive autoimmune condition that culminates in the loss of insulin-producing beta cells. Pancreatic histopathology provides essential insights into disease initiation and progression yet an integrated perspective of pathogenic processes is lacking due to limited sample availability, the dispersed nature of anatomical lesions, and often restricted analytical dimensionality. Here, we combined multiplexed immunostaining, high-magnification whole-slide imaging, digital pathology, and semi-automated image analysis strategies to interrogate pancreatic tail and head regions obtained from organ donors 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 revealed a series of novel histopathological correlates especially in the prodromal disease stage preceding clinical T1D. Altogether, our comprehensive "single-islet" analyses permit the reconstruction of a revised natural T1D history with implications for further histopathological investigations, considerations of pathogenetic modalities, and therapeutic interventions.

摘要

1型糖尿病(T1D)是一种渐进性自身免疫性疾病,最终导致产生胰岛素的β细胞丧失。胰腺组织病理学为疾病的起始和进展提供了重要见解,但由于样本可用性有限、解剖病变的分散性质以及通常受限的分析维度,缺乏对致病过程的综合观点。在此,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策略,以研究从处于T1D各个阶段(包括高危和发病期病例)的器官捐赠者获得的胰腺尾部和头部区域。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解卷积分析,揭示了一系列新的组织病理学相关性,尤其是在临床T1D之前的前驱疾病阶段。总之,我们全面的“单胰岛”分析允许重建修订后的T1D自然病程,这对进一步的组织病理学研究、致病模式的考量以及治疗干预具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d2b/11956956/52386c58fb0f/nihpp-2025.03.18.644000v1-f0001.jpg

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