Department of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Department of Medicine, Division of Hematology/Oncology, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Sci Rep. 2022 Jan 11;12(1):559. doi: 10.1038/s41598-021-04286-5.
Identification of cognate interactions between antigen-specific T cells and dendritic cells (DCs) is essential to understanding immunity and tolerance, and for developing therapies for cancer and autoimmune diseases. Conventional techniques for selecting antigen-specific T cells are time-consuming and limited to pre-defined antigenic peptide sequences. Here, we demonstrate the ability to use deep learning to rapidly classify videos of antigen-specific CD8 T cells. The trained model distinguishes distinct interaction dynamics (in motility and morphology) between cognate and non-cognate T cells and DCs over 20 to 80 min. The model classified high affinity antigen-specific CD8 T cells from OT-I mice with an area under the curve (AUC) of 0.91, and generalized well to other types of high and low affinity CD8 T cells. The classification accuracy achieved by the model was consistently higher than simple image analysis techniques, and conventional metrics used to differentiate between cognate and non-cognate T cells, such as speed. Also, we demonstrated that experimental addition of anti-CD40 antibodies improved model prediction. Overall, this method demonstrates the potential of video-based deep learning to rapidly classify cognate T cell-DC interactions, which may also be potentially integrated into high-throughput methods for selecting antigen-specific T cells in the future.
鉴定抗原特异性 T 细胞与树突状细胞(DCs)之间的同源相互作用对于理解免疫和耐受以及开发癌症和自身免疫性疾病的治疗方法至关重要。选择抗原特异性 T 细胞的传统技术既耗时又限于预先定义的抗原肽序列。在这里,我们展示了使用深度学习快速分类抗原特异性 CD8 T 细胞视频的能力。经过训练的模型可以区分同源和非同源 T 细胞与 DC 之间 20 到 80 分钟的不同相互作用动力学(在运动和形态上)。该模型以 0.91 的曲线下面积(AUC)从 OT-I 小鼠中分类高亲和力抗原特异性 CD8 T 细胞,并且很好地推广到其他类型的高亲和性和低亲和性 CD8 T 细胞。该模型的分类准确性始终高于简单的图像分析技术,以及传统的用于区分同源和非同源 T 细胞的指标,例如速度。此外,我们证明了添加抗 CD40 抗体可改善模型预测。总体而言,该方法证明了基于视频的深度学习快速分类同源 T 细胞-DC 相互作用的潜力,该方法将来也可能集成到高通量选择抗原特异性 T 细胞的方法中。