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首页> 外文期刊>Cytotherapy >Morphological profiling using machine learning reveals emergent subpopulations of interferon-gamma-stimulated mesenchymal stromal cells that predict immunosuppression
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Morphological profiling using machine learning reveals emergent subpopulations of interferon-gamma-stimulated mesenchymal stromal cells that predict immunosuppression

机译:使用机器学习的形态分析显示了预测免疫抑制的干扰素-γ刺激的间充质细胞的突出亚体

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摘要

Background: Although a preponderance of pre-clinical data demonstrates the immunosuppressive potential of mesenchymal stromal cells (MSCs), significant heterogeneity and lack of critical quality attributes (CQAs) based on immunosuppressive capacity likely have contributed to inconsistent clinical outcomes. This heterogeneity exists not only between MSC lots derived from different donors, tissues and manufacturing conditions, but also within a given MSC lot in the form of functional subpopulations. We therefore explored the potential of functionally relevant morphological profiling (FRMP) to identify morphological subpopulations predictive of the immunosuppressive capacity of MSCs derived from multiple donors, manufacturers and passages. Methods: We profiled the single-cell morphological response of MSCs from different donors and passages to the functionally relevant inflammatory cytokine interferon (IFN)-gamma. We used the machine learning approach visual stochastic neighbor embedding (viSNE) to identify distinct morphological subpopulations that could predict suppression of activated CD4(+) and CD8(+) T cells in a multiplexed quantitative assay. Results: Multiple IFN-gamma- stimulated subpopulations significantly correlated with the ability of MSCs to inhibit CD4(+) and CD8(+) T-cell activation and served as effective CQAs to predict the immunosuppressive capacity of additional manufactured MSC lots. We further characterized the emergence of morphological heterogeneity following IFN-gamma stimulation, which provides a strategy for identifying functional subpopulations for future single-cell characterization and enrichment techniques. Discussion: This work provides a generalizable analytical platform for assessing functional heterogeneity based on single-cell morphological responses that could be used to identify novel CQAs and inform cell manufacturing decisions.
机译:背景:虽然前临床前数据的优势表现出间充质基质细胞(MSCs)的免疫抑制潜力,但基于免疫抑制容量的显着异质性和缺乏关键质量属性(CQAS)可能导致不一致的临床结果。该异质性不仅存在于来自不同供体,组织和制造条件的MSC批次之间,而且存在于给定的MSC批次中以功能性亚步骤的形式。因此,我们探讨了功能相关的形态分析(FRMP)的潜力,以确定预测来自多个捐赠者,制造商和通道的MSCs的免疫抑制能力的形态亚群。方法:对不同供体和通道的MSCs的单细胞形态反应分解给功能相关的炎性细胞因子干扰素(IFN)-γ。我们使用机器学习方法视觉随机邻居嵌入(Visne),以识别可以预测多路复用定量​​测定中的激活CD4(+)和CD8(+)T细胞的不同形态亚群。结果:多种IFN-γ-刺激的亚ppopulation与MSCs抑制CD4(+)和CD8(+)T细胞活化的能力显着相关,并用作有效的CQA,以预测额外制造的MSC批次的免疫抑制能力。我们进一步表征了IFN-Gamma刺激后形态异质性的出现,这提供了识别未来单细胞表征和富集技术的功能性亚族的策略。讨论:这项工作提供了一种可宽容化的分析平台,用于基于单细胞形态响应来评估功能异质性,可用于识别新型CQAS并告知细胞制造决策。

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