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使用多模态学习进行细胞核亚型分类。

Nucleus subtype classification using inter-modality learning.

作者信息

Remedios Lucas W, Bao Shunxing, Remedios Samuel W, Lee Ho Hin, Cai Leon Y, Li Thomas, Deng Ruining, Cui Can, Li Jia, Liu Qi, Lau Ken S, Roland Joseph T, Washington Mary K, Coburn Lori A, Wilson Keith T, Huo Yuankai, Landman Bennett A

机构信息

Vanderbilt University, Department of Computer Science, Nashville, USA.

Vanderbilt University, Department of Electrical and Computer Engineering, Nashville, USA.

出版信息

Proc SPIE Int Soc Opt Eng. 2024 Feb;12933. doi: 10.1117/12.3006237. Epub 2024 Apr 3.

DOI:10.1117/12.3006237
PMID:39268202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11392413/
Abstract

Understanding the way cells communicate, co-locate, and interrelate is essential to understanding human physiology. Hematoxylin and eosin (H&E) staining is ubiquitously available both for clinical studies and research. The Colon Nucleus Identification and Classification (CoNIC) Challenge has recently innovated on robust artificial intelligence labeling of six cell types on H&E stains of the colon. However, this is a very small fraction of the number of potential cell classification types. Specifically, the CoNIC Challenge is unable to classify epithelial subtypes (progenitor, endocrine, goblet), lymphocyte subtypes (B, helper T, cytotoxic T), or connective subtypes (fibroblasts, stromal). In this paper, we propose to use inter-modality learning to label previously un-labelable cell types on virtual H&E. We leveraged multiplexed immunofluorescence (MxIF) histology imaging to identify 14 subclasses of cell types. We performed style transfer to synthesize virtual H&E from MxIF and transferred the higher density labels from MxIF to these virtual H&E images. We then evaluated the efficacy of learning in this approach. We identified helper T and progenitor nuclei with positive predictive values of 0.34 ± 0.15 (prevalence 0.03 ± 0.01) and 0.47 ± 0.1 (prevalence 0.07 ± 0.02) respectively on virtual H&E. This approach represents a promising step towards automating annotation in digital pathology.

摘要

了解细胞间如何进行通讯、共定位和相互关联对于理解人体生理学至关重要。苏木精和伊红(H&E)染色在临床研究和科研中广泛可用。结肠细胞核识别与分类(CoNIC)挑战赛最近在结肠H&E染色上对六种细胞类型进行强大的人工智能标记方面取得了创新。然而,这只是潜在细胞分类类型数量的极小一部分。具体而言,CoNIC挑战赛无法对上皮亚型(祖细胞、内分泌细胞、杯状细胞)、淋巴细胞亚型(B细胞、辅助性T细胞、细胞毒性T细胞)或结缔组织亚型(成纤维细胞、基质细胞)进行分类。在本文中,我们建议使用多模态学习来标记虚拟H&E上以前无法标记的细胞类型。我们利用多重免疫荧光(MxIF)组织学成像来识别14种细胞类型亚类。我们进行了风格迁移,从MxIF合成虚拟H&E,并将MxIF上更高密度的标签转移到这些虚拟H&E图像上。然后我们评估了这种方法中的学习效果。我们在虚拟H&E上分别识别出辅助性T细胞核和祖细胞核,其阳性预测值分别为0.34±0.15(患病率0.03±0.01)和0.47±0.1(患病率0.07±0.02)。这种方法代表了数字病理学中自动化注释的一个有前景的进展。

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引用本文的文献

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Data-driven nucleus subclassification on colon hematoxylin and eosin using style-transferred digital pathology.利用风格迁移数字病理学对结肠苏木精和伊红染色切片进行数据驱动的细胞核亚分类
J Med Imaging (Bellingham). 2024 Nov;11(6):067501. doi: 10.1117/1.JMI.11.6.067501. Epub 2024 Nov 5.

本文引用的文献

1
Alleviating tiling effect by random walk sliding window in high-resolution histological whole slide image synthesis.通过随机游走滑动窗口减轻高分辨率组织学全切片图像合成中的平铺效应。
Proc Mach Learn Res. 2024;227:1406-1422.
2
DeepCell Kiosk: scaling deep learning-enabled cellular image analysis with Kubernetes.DeepCell 自助服务亭:使用 Kubernetes 扩展支持深度学习的细胞图像分析。
Nat Methods. 2021 Jan;18(1):43-45. doi: 10.1038/s41592-020-01023-0. Epub 2021 Jan 4.
3
Tissue processing and hematoxylin and eosin staining.组织处理及苏木精-伊红染色
Methods Mol Biol. 2014;1180:31-43. doi: 10.1007/978-1-4939-1050-2_3.
4
Highly multiplexed single-cell analysis of formalin-fixed, paraffin-embedded cancer tissue.福尔马林固定石蜡包埋肿瘤组织的高多重化单细胞分析。
Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11982-7. doi: 10.1073/pnas.1300136110. Epub 2013 Jul 1.