CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:DIISCO: A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data.
DIISCO: A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
表征细胞间通讯并追踪其随时间变化,对于理解协调正常发育、疾病进展或治疗等扰动应答的生物过程至关重要。现有工具缺乏捕捉治疗等因素影响下、具有时间依赖性的细胞间相互作用的能力,且主要依赖在有限情境下编制的既有数据库。我们提出DIISCO,这是一种基于贝叶斯框架的方法,利用多个时间点的单细胞RNA测序数据表征细胞相互作用的时间动态。该方法采用结构化高斯过程回归,根据不同细胞类型共同演化的情况揭示时间分辨的相互作用,并纳入受体-配体复合物的先验知识。我们利用模拟数据,以及新采集的CAR-T 细胞与淋巴瘤细胞共培养数据,展示了DIISCO的可解释性,说明其有望揭示动态细胞间串扰。
Characterizing cell-cell communication and tracking its variability over time is essential for understanding the coordination of biological processes mediating normal development, progression of disease, or responses to perturbations such as therapies. Existing tools lack the ability to capture time-dependent intercellular interactions, such as those influenced by therapy, and primarily rely on existing databases compiled from limited contexts.
We present DIISCO, a Bayesian framework for characterizing the temporal dynamics of cellular interactions using single-cell RNA-sequencing data from multiple time points.
Our method uses structured Gaussian process regression to unveil time-resolved interactions among diverse cell types according to their co-evolution and incorporates prior knowledge of receptor-ligand complexes.
We show the interpretability of DIISCO in simulated data and new data collected from CAR-T cells co-cultured with lymphoma cells, demonstrating its potential to uncover dynamic cell-cell crosstalk.
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