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      Integrated workflow for analysis of immune enriched spatial proteomic data with IMmuneCite

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          Abstract

          Spatial proteomics enable detailed analysis of tissue at single cell resolution. However, creating reliable segmentation masks and assigning accurate cell phenotypes to discrete cellular phenotypes can be challenging. We introduce IMmuneCite, a computational framework for comprehensive image pre-processing and single-cell dataset creation, focused on defining complex immune landscapes when using spatial proteomics platforms. We demonstrate that IMmuneCite facilitates the identification of 32 discrete immune cell phenotypes using data from human liver samples while substantially reducing nonbiological cell clusters arising from co-localization of markers for different cell lineages. We established its versatility and ability to accommodate any antibody panel and different species by applying IMmuneCite to data from murine liver tissue. This approach enabled deep characterization of different functional states in each immune compartment, uncovering key features of the immune microenvironment in clinical liver transplantation and murine hepatocellular carcinoma. In conclusion, we demonstrated that IMmuneCite is a user-friendly, integrated computational platform that facilitates investigation of the immune microenvironment across species, while ensuring the creation of an immune focused, spatially resolved single-cell proteomic dataset to provide high fidelity, biologically relevant analyses.

          Supplementary Information

          The online version contains supplementary material available at 10.1038/s41598-025-93060-y.

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          Most cited references63

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          scikit-image: image processing in Python

          scikit-image is an image processing library that implements algorithms and utilities for use in research, education and industry applications. It is released under the liberal Modified BSD open source license, provides a well-documented API in the Python programming language, and is developed by an active, international team of collaborators. In this paper we highlight the advantages of open source to achieve the goals of the scikit-image library, and we showcase several real-world image processing applications that use scikit-image. More information can be found on the project homepage, http://scikit-image.org.
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            ilastik: interactive machine learning for (bio)image analysis

            We present ilastik, an easy-to-use interactive tool that brings machine-learning-based (bio)image analysis to end users without substantial computational expertise. It contains pre-defined workflows for image segmentation, object classification, counting and tracking. Users adapt the workflows to the problem at hand by interactively providing sparse training annotations for a nonlinear classifier. ilastik can process data in up to five dimensions (3D, time and number of channels). Its computational back end runs operations on-demand wherever possible, allowing for interactive prediction on data larger than RAM. Once the classifiers are trained, ilastik workflows can be applied to new data from the command line without further user interaction. We describe all ilastik workflows in detail, including three case studies and a discussion on the expected performance.
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              Data-Driven Phenotypic Dissection of AML Reveals Progenitor-like Cells that Correlate with Prognosis.

              Acute myeloid leukemia (AML) manifests as phenotypically and functionally diverse cells, often within the same patient. Intratumor phenotypic and functional heterogeneity have been linked primarily by physical sorting experiments, which assume that functionally distinct subpopulations can be prospectively isolated by surface phenotypes. This assumption has proven problematic, and we therefore developed a data-driven approach. Using mass cytometry, we profiled surface and intracellular signaling proteins simultaneously in millions of healthy and leukemic cells. We developed PhenoGraph, which algorithmically defines phenotypes in high-dimensional single-cell data. PhenoGraph revealed that the surface phenotypes of leukemic blasts do not necessarily reflect their intracellular state. Using hematopoietic progenitors, we defined a signaling-based measure of cellular phenotype, which led to isolation of a gene expression signature that was predictive of survival in independent cohorts. This study presents new methods for large-scale analysis of single-cell heterogeneity and demonstrates their utility, yielding insights into AML pathophysiology.
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                Author and article information

                Contributors
                Juliet.Emamaullee@med.usc.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                19 March 2025
                19 March 2025
                2025
                : 15
                : 9394
                Affiliations
                [1 ]Division of Abdominal Organ Transplantation and Hepatobiliary Surgery, Department of Surgery, Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) 1510 San Pablo Street, Suite 412, Los Angeles, CA 90033 USA
                [2 ]Department of Surgery, University of Rochester, ( https://ror.org/022kthw22) Rochester, NY USA
                [3 ]Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [4 ]Division of Oncology, Department of Medicine, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [5 ]Division of Gastroenterology, Hepatology and Nutrition, Children’s Hospital of Los Angeles, ( https://ror.org/00412ts95) Los Angeles, CA USA
                [6 ]Department of Medicine, Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [7 ]Division of Abdominal Organ Transplantation, Children’s Hospital of Los Angeles, ( https://ror.org/00412ts95) Los Angeles, CA USA
                Author information
                http://orcid.org/0000-0001-7062-3236
                http://orcid.org/0000-0002-7952-0679
                http://orcid.org/0000-0001-8681-8257
                http://orcid.org/0000-0002-3664-4946
                http://orcid.org/0000-0002-0740-5102
                http://orcid.org/0000-0002-0198-7703
                http://orcid.org/0000-0002-6853-9884
                http://orcid.org/0000-0003-4238-3057
                Article
                93060
                10.1038/s41598-025-93060-y
                11920390
                40102469
                917ac58c-cb87-41cd-aa0a-a4255938eb26
                © The Author(s) 2025

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

                History
                : 9 August 2024
                : 4 March 2025
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100007557, California Institute of Regenerative Medicine;
                Award ID: Fellowship Training Grant
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100016621, OneLegacy Foundation;
                Award ID: Fellowship Training Grant
                Award Recipient :
                Funded by: National Cancer Institute
                Award ID: K08CA245220
                Award Recipient :
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2025

                Uncategorized
                single cell proteomics,spatial biology,informatics pipeline,immune microenvironment,data processing,image processing,translational immunology,transplant immunology

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