TY - JOUR
T1 - Deep Learning–Based H-Score Quantification of Immunohistochemistry-Stained Images
AU - Wen, Zhuoyu
AU - Luo, Danni
AU - Wang, Shidan
AU - Rong, Ruichen
AU - Evers, Bret M.
AU - Jia, Liwei
AU - Fang, Yisheng
AU - Daoud, Elena V.
AU - Yang, Shengjie
AU - Gu, Zifan
AU - Arner, Emily N.
AU - Lewis, Cheryl M.
AU - Solis Soto, Luisa M.
AU - Fujimoto, Junya
AU - Behrens, Carmen
AU - Wistuba, Ignacio I.
AU - Yang, Donghan M.
AU - Brekken, Rolf A.
AU - O'Donnell, Kathryn A.
AU - Xie, Yang
AU - Xiao, Guanghua
N1 - Publisher Copyright:
© 2023 United States & Canadian Academy of Pathology
PY - 2024/2
Y1 - 2024/2
N2 - 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.
AB - 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.
KW - H-score
KW - deep learning
KW - immunohistochemistry image
KW - pathology image analysis
KW - protein expression quantification
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U2 - 10.1016/j.modpat.2023.100398
DO - 10.1016/j.modpat.2023.100398
M3 - Article
C2 - 38043788
AN - SCOPUS:85182899392
SN - 0893-3952
VL - 37
JO - Modern Pathology
JF - Modern Pathology
IS - 2
M1 - 100398
ER -