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

IF 14.3 1区 医学 Q1 CELL & TISSUE ENGINEERING Bone Research Pub Date : 2024-09-27 DOI:10.1038/s41413-024-00359-z
Ryan A. Lacinski, Sebastian A. Dziadowicz, Vincent K. Melemai, Brody Fitzpatrick, John J. Pisquiy, Tanya Heim, Ines Lohse, Karen E. Schoedel, Nicolas J. Llosa, Kurt R. Weiss, Brock A. Lindsey
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Abstract

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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空间多重免疫荧光分析揭示了与转移性骨肉瘤总存活率相关的协调细胞网络
被确诊为晚期骨肉瘤(通常是肺转移瘤)的患者五年总生存率极低。骨肉瘤免疫肿瘤微环境的复杂性是各种免疫疗法临床试验失败的原因之一。这项探索性研究旨在从空间上描述转移性骨肉瘤肺部标本的免疫肿瘤微环境。了解这些组织内的协调细胞网络,有助于在利用免疫疗法治疗这种疾病时提高疗效。重要的是,各种细胞类型、相互作用和细胞邻域与五年生存状况有关。值得注意的是,在5年存活的患者队列中观察到T淋巴细胞、程序性细胞死亡蛋白1阳性细胞和髓源性抑制细胞之间的细胞相互作用增加。此外,细胞邻域分析还发现了免疫-冷实质细胞邻域,这也与5年生存率较低有关。最后,骨肉瘤空间评分(Osteosarcoma Spatial Score)通过免疫细胞和肿瘤细胞的空间邻近性来近似反映免疫肿瘤微环境中的效应免疫活动,5 年存活者的这一评分有所提高,表明该患者队列中的效应信号得到了改善。最终,这些数据代表了对转移性骨肉瘤免疫肿瘤微环境的可靠空间多重免疫荧光分析。研究描述了各种通讯网络及其与生存的关系。未来,对这些网络的识别可能会建议使用特定的联合免疫治疗策略,以改善骨肉瘤的抗肿瘤免疫反应和预后。
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来源期刊
Bone Research
Bone Research CELL & TISSUE ENGINEERING-
CiteScore
20.00
自引率
4.70%
发文量
289
审稿时长
20 weeks
期刊介绍: Established in 2013, Bone Research is a newly-founded English-language periodical that centers on the basic and clinical facets of bone biology, pathophysiology, and regeneration. It is dedicated to championing key findings emerging from both basic investigations and clinical research concerning bone-related topics. The journal's objective is to globally disseminate research in bone-related physiology, pathology, diseases, and treatment, contributing to the advancement of knowledge in this field.
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