Quantitative Biomedical Research Center, Peter O'Donnell Jr School of Public Health, The University of Texas Southwestern Medical Center, Dallas, Texas.
Department of Pathology, The University of Texas Southwestern Medical Center, Dallas, Texas.
Mod Pathol. 2024 Feb;37(2):100398. doi: 10.1016/j.modpat.2023.100398. Epub 2023 Dec 1.
Immunohistochemistry (IHC) is a well-established and commonly used staining method for clinical diagnosis and biomedical research. In most IHC images, the target protein is conjugated with a specific antibody and stained using diaminobenzidine (DAB), resulting in a brown coloration, whereas hematoxylin serves as a blue counterstain for cell nuclei. The protein expression level is quantified through the H-score, calculated from DAB staining intensity within the target cell region. Traditionally, this process requires evaluation by 2 expert pathologists, which is both time consuming and subjective. To enhance the efficiency and accuracy of this process, we have developed an automatic algorithm for quantifying the H-score of IHC images. To characterize protein expression in specific cell regions, a deep learning model for region recognition was trained based on hematoxylin staining only, achieving pixel accuracy for each class ranging from 0.92 to 0.99. Within the desired area, the algorithm categorizes DAB intensity of each pixel as negative, weak, moderate, or strong staining and calculates the final H-score based on the percentage of each intensity category. Overall, this algorithm takes an IHC image as input and directly outputs the H-score within a few seconds, significantly enhancing the speed of IHC image analysis. This automated tool provides H-score quantification with precision and consistency comparable to experienced pathologists but at a significantly reduced cost during IHC diagnostic workups. It holds significant potential to advance biomedical research reliant on IHC staining for protein expression quantification.
免疫组织化学(IHC)是一种成熟且常用的临床诊断和生物医学研究染色方法。在大多数 IHC 图像中,目标蛋白与特定抗体结合,并使用二氨基联苯胺(DAB)进行染色,产生棕色着色,而苏木精则作为细胞核的蓝色对照染色。通过 H 评分对蛋白表达水平进行量化,该评分是通过目标细胞区域内 DAB 染色强度计算得出的。传统上,这一过程需要两位专家病理学家进行评估,既耗时又主观。为了提高这一过程的效率和准确性,我们开发了一种用于量化 IHC 图像 H 评分的自动算法。为了对特定细胞区域的蛋白表达进行特征化,我们仅基于苏木精染色训练了一个用于区域识别的深度学习模型,每个类别的像素准确率在 0.92 到 0.99 之间。在所需区域内,该算法将每个像素的 DAB 强度分类为阴性、弱阳性、中度阳性或强阳性,并根据每个强度类别的百分比计算最终 H 评分。总的来说,该算法以 IHC 图像作为输入,几秒钟内即可直接输出 H 评分,显著提高了 IHC 图像分析的速度。与经验丰富的病理学家相比,这种自动化工具在 IHC 诊断工作中提供了具有可比性的 H 评分定量精度和一致性,但成本却大大降低。它在依赖 IHC 染色进行蛋白表达定量的生物医学研究中具有重要的应用潜力。