Evaluating predictive patterns of antigen-specific B cells by single-cell transcriptome and antibody repertoire sequencing
Publication date
2024-12-18
Authors
Erlach, Lena
Kuhn, Raphael
Agrafiotis, Andreas
Shlesinger, Danielle
Yermanos, Alexander
Reddy, Sai T.
Editors
Advisors
Supervisors
Document Type
Article
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cc_by
Abstract
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.
Keywords
antibody repertoire sequencing, antigen-specific B cells, antigen-specificity prediction, B cell immune response, machine learning for antibody discovery, single-cell sequencing dataset, single-cell transcriptome sequencing, Pathology and Forensic Medicine, Histology, Cell Biology
Citation
Erlach, L, Kuhn, R, Agrafiotis, A, Shlesinger, D, Yermanos, A & Reddy, S T 2024, 'Evaluating predictive patterns of antigen-specific B cells by single-cell transcriptome and antibody repertoire sequencing', Cell Systems, vol. 15, no. 12, pp. 1295-1303.e5. https://doi.org/10.1016/j.cels.2024.11.005