通过单细胞转录组和抗体库测序评估抗原特异性B细胞的预测模式。

Cell systems Pub Date : 2024-12-18 Epub Date: 2024-12-10 DOI:10.1016/j.cels.2024.11.005
Lena Erlach, Raphael Kuhn, Andreas Agrafiotis, Danielle Shlesinger, Alexander Yermanos, Sai T Reddy
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引用次数: 0

摘要

抗体发现领域通常涉及对免疫动物的B细胞进行广泛的实验筛选。机器学习(ML)引导的抗原特异性B细胞预测可以加速这一过程,但需要足够的抗原特异性标记训练数据。在这里,我们介绍了免疫小鼠B细胞的单细胞转录组和抗体库测序数据集,这些B细胞通过实验选择被标记为抗原特异性或非特异性。我们通过差异基因表达分析确定与抗原特异性相关的基因表达模式,并评估其抗体序列多样性。随后,我们对各种ML模型进行了基准测试,包括线性和非线性模型,对基因表达和抗体库特征的不同组合进行了训练。此外,我们使用通用和抗体特异性蛋白质语言模型(PLMs)的特征来评估迁移学习。我们的研究结果表明,基于基因表达的模型在抗原特异性预测方面优于基于序列的模型,这为计算指导的抗体发现提供了一条有前途的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating predictive patterns of antigen-specific B cells by single-cell transcriptome and antibody repertoire sequencing.

The field of antibody discovery typically involves extensive experimental screening of B cells from immunized animals. Machine learning (ML)-guided prediction of antigen-specific B cells could accelerate this process but requires sufficient training data with antigen-specificity labeling. Here, we introduce a dataset of single-cell transcriptome and antibody repertoire sequencing of B cells from immunized mice, which are labeled as antigen specific or non-specific through experimental selections. We identify gene expression patterns associated with antigen specificity by differential gene expression analysis and assess their antibody sequence diversity. Subsequently, we benchmark various ML models, both linear and non-linear, trained on different combinations of gene expression and antibody repertoire features. Additionally, we assess transfer learning using features from general and antibody-specific protein language models (PLMs). Our findings show that gene expression-based models outperform sequence-based models for antigen-specificity predictions, highlighting a promising avenue for computationally guided antibody discovery.

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