Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue

Abstract The availability of target cells expressing the HIV receptors CD4 and CCR5 in genital tissue is a critical determinant of HIV susceptibility during sexual transmission. Quantification of immune cells in genital tissue is therefore an important outcome for studies on HIV susceptibility and p...

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Published in:Scientific Reports
Main Authors: Zhongtian Shao, Lane B. Buchanan, David Zuanazzi, Yazan N. Khan, Ali R. Khan, Jessica L. Prodger
Format: Article
Language:English
Published: Nature Portfolio 2024-01-01
Online Access:https://doi.org/10.1038/s41598-024-52613-3
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author Zhongtian Shao
Lane B. Buchanan
David Zuanazzi
Yazan N. Khan
Ali R. Khan
Jessica L. Prodger
author_facet Zhongtian Shao
Lane B. Buchanan
David Zuanazzi
Yazan N. Khan
Ali R. Khan
Jessica L. Prodger
author_sort Zhongtian Shao
collection DOAJ
container_title Scientific Reports
description Abstract The availability of target cells expressing the HIV receptors CD4 and CCR5 in genital tissue is a critical determinant of HIV susceptibility during sexual transmission. Quantification of immune cells in genital tissue is therefore an important outcome for studies on HIV susceptibility and prevention. Immunofluorescence microscopy allows for precise visualization of immune cells in mucosal tissues; however, this technique is limited in clinical studies by the lack of an accurate, unbiased, high-throughput image analysis method. Current pixel-based thresholding methods for cell counting struggle in tissue regions with high cell density and autofluorescence, both of which are common features in genital tissue. We describe a deep-learning approach using the publicly available StarDist method to count cells in immunofluorescence microscopy images of foreskin stained for nuclei, CD3, CD4, and CCR5. The accuracy of the model was comparable to manual counting (gold standard) and surpassed the capability of a previously described pixel-based cell counting method. We show that the performance of our deep-learning model is robust in tissue regions with high cell density and high autofluorescence. Moreover, we show that this deep-learning analysis method is both easy to implement and to adapt for the identification of other cell types in genital mucosal tissue.
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spelling doaj-art-6bc01dc45f5f4cd6b8b18481ae4de7db2025-08-19T22:58:55ZengNature PortfolioScientific Reports2045-23222024-01-0114111310.1038/s41598-024-52613-3Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissueZhongtian Shao0Lane B. Buchanan1David Zuanazzi2Yazan N. Khan3Ali R. Khan4Jessica L. Prodger5Department of Microbiology and Immunology, The University of Western OntarioDepartment of Microbiology and Immunology, The University of Western OntarioDepartment of Microbiology and Immunology, The University of Western OntarioDepartment of Microbiology and Immunology, The University of Western OntarioDepartment of Medical Biophysics, The University of Western OntarioDepartment of Microbiology and Immunology, The University of Western OntarioAbstract The availability of target cells expressing the HIV receptors CD4 and CCR5 in genital tissue is a critical determinant of HIV susceptibility during sexual transmission. Quantification of immune cells in genital tissue is therefore an important outcome for studies on HIV susceptibility and prevention. Immunofluorescence microscopy allows for precise visualization of immune cells in mucosal tissues; however, this technique is limited in clinical studies by the lack of an accurate, unbiased, high-throughput image analysis method. Current pixel-based thresholding methods for cell counting struggle in tissue regions with high cell density and autofluorescence, both of which are common features in genital tissue. We describe a deep-learning approach using the publicly available StarDist method to count cells in immunofluorescence microscopy images of foreskin stained for nuclei, CD3, CD4, and CCR5. The accuracy of the model was comparable to manual counting (gold standard) and surpassed the capability of a previously described pixel-based cell counting method. We show that the performance of our deep-learning model is robust in tissue regions with high cell density and high autofluorescence. Moreover, we show that this deep-learning analysis method is both easy to implement and to adapt for the identification of other cell types in genital mucosal tissue.https://doi.org/10.1038/s41598-024-52613-3
spellingShingle Zhongtian Shao
Lane B. Buchanan
David Zuanazzi
Yazan N. Khan
Ali R. Khan
Jessica L. Prodger
Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue
title Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue
title_full Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue
title_fullStr Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue
title_full_unstemmed Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue
title_short Comparison between a deep-learning and a pixel-based approach for the automated quantification of HIV target cells in foreskin tissue
title_sort comparison between a deep learning and a pixel based approach for the automated quantification of hiv target cells in foreskin tissue
url https://doi.org/10.1038/s41598-024-52613-3
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