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Spatial multiplexed immunofluorescence analysis reveals coordinated cellular networks associated with overall survival in metastatic osteosarcoma

摘要Patients diagnosed with advanced osteosarcoma,often in the form of lung metastases,have abysmal five-year overall survival rates.The complexity of the osteosarcoma immune tumor microenvironment has been implicated in clinical trial failures of various immunotherapies.The purpose of this exploratory study was to spatially characterize the immune tumor microenvironment of metastatic osteosarcoma lung specimens.Knowledge of the coordinating cellular networks within these tissues could then lead to improved outcomes when utilizing immunotherapy for treatment of this disease.Importantly,various cell types,interactions,and cellular neighborhoods were associated with five-year survival status.Of note,increases in cellular interactions between T lymphocytes,positive for programmed cell death protein 1,and myeloid-derived suppressor cells were observed in the 5-year deceased cohort.Additionally,cellular neighborhood analysis identified an Immune-Cold Parenchyma cellular neighborhood,also associated with worse 5-year survival.Finally,the Osteosarcoma Spatial Score,which approximates effector immune activity in the immune tumor microenvironment through the spatial proximity of immune and tumor cells,was increased within 5-year survivors,suggesting improved effector signaling in this patient cohort.Ultimately,these data represent a robust spatial multiplexed immunofluorescence analysis of the metastatic osteosarcoma immune tumor microenvironment.Various communication networks,and their association with survival,were described.In the future,identification of these networks may suggest the use of specific,combinatory immunotherapeutic strategies for improved anti-tumor immune responses and outcomes in osteosarcoma.

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作者 Ryan A.Lacinski [1] Sebastian A.Dziadowicz [2] Vincent K.Melemai [3] Brody Fitzpatrick [3] John J.Pisquiy [3] Tanya Heim [4] Ines Lohse [4] Karen E.Schoedel [5] Nicolas J.Llosa [6] Kurt R.Weiss [4] Brock A.Lindsey [6] 学术成果认领
作者单位 Department of Orthopaedics,West Virginia University School of Medicine,Morgantown,WV 26506,USA;Cancer Institute,West Virginia University School of Medicine,Morgantown,WV 26506,USA [1] Department of Microbiology,Immunology and Cell Biology,West Virginia University School of Medicine,Morgantown,WV 26506,USA;Bioinformatics Core,West Virginia University School of Medicine,Morgantown,WV 26506,USA [2] Department of Orthopaedics,West Virginia University School of Medicine,Morgantown,WV 26506,USA [3] Department of Orthopaedic Surgery,University of Pittsburgh Medical Center,Pittsburgh,PA 15213,USA [4] Department of Pathology,University of Pittsburgh Medical Center,Pittsburgh,PA 15213,USA [5] Department of Orthopaedic Surgery,Johns Hopkins University School of Medicine,Baltimore,MD 21287,USA [6]
栏目名称 ORIGINAL ARTICLES
DOI 10.1038/s41413-024-00359-z
发布时间 2025-02-25
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骨研究(英文版)

骨研究(英文版)

2024年12卷4期

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