Convergent selection in antibody repertoires is revealed by deep learning
Friedensohn, S.; Neumeier, D.; Khan, T. A.; Csepregi, L.; Parola, C.; de Vries, A. R. G.; Erlach, L.; Mason, D. M.; Reddy, S. T.
Show abstract
Adaptive immunity is driven by the ability of lymphocytes to undergo V(D)J recombination and generate a highly diverse set of immune receptors (B cell receptors/secreted antibodies and T cell receptors) and their subsequent clonal selection and expansion upon molecular recognition of foreign antigens. These principles lead to remarkable, unique and dynamic immune receptor repertoires1. Deep sequencing provides increasing evidence for the presence of commonly shared (convergent) receptors across individual organisms within one species2-4. Convergent selection of specific receptors towards various antigens offers one explanation for these findings. For example, single cases of convergence have been reported in antibody repertoires of viral infection or allergy5-8. Recent studies demonstrate that convergent selection of sequence motifs within T cell receptor (TCR) repertoires can be identified on an even wider scale9,10. Here we report that there is extensive convergent selection in antibody repertoires of mice for a range of protein antigens and immunization conditions. We employed a deep learning approach utilizing variational autoencoders (VAEs) to model the underlying process of B cell receptor (BCR) recombination and assume that the data generation follows a Gaussian mixture model (GMM) in latent space. This provides both a latent embedding and cluster labels that group similar sequences, thus enabling the discovery of a multitude of convergent, antigen-associated sequence patterns. Using a linear, one-versus-all support vector machine (SVM), we confirm that the identified sequence patterns are predictive of antigenic exposure and outperform predictions based on the occurrence of public clones. Recombinant expression of both natural and in silico-generated antibodies possessing convergent patterns confirms their binding specificity to target antigens. Our work highlights to which extent convergence in antibody repertoires can occur and shows how deep learning can be applied for immunodiagnostics and antibody discovery and engineering.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- APMAT analysis reveals the association between CD8 T cell receptors, cognate antigen, and T cell phenotype and persistence 97%
- LAG-3 blockade reactivates the CD8+ T cell expansion program to re-expand contracted clones in the tumor 96%
- Optimizing a Human Monoclonal Antibody for Better Neutralization of SARS-CoV-2 96%
Similar papers in this journal
- High-Throughput and High-Dimensional Single Cell Analysis of Antigen-Specific CD8+ T cells 97%
- SARS-CoV-2 antigen exposure history shapes phenotypes and specificity of memory CD8 T cells 96%
- Loss of the intracellular enzyme QPCTL limits chemokine function and reshapes myeloid infiltration to augment tumor immunity 95%
Similar papers in this journal
- Full-spike deep mutational scanning helps predict the evolutionary success of SARS-CoV-2 clades 96%
- Impact of circulating SARS-CoV-2 variants on mRNA vaccine-induced immunity in uninfected and previously infected individuals 96%
- RIFINs displayed on malaria-infected erythrocytes bind both KIR2DL1 and KIR2DS1 96%
Similar papers in this journal
- Human thymopoiesis produces polyspecific CD8+ alfa/beta T cells responding to multiple viral antigens 96%
- Hierarchical sequence-affinity landscapes shape the evolution of breadth in an anti-influenza receptor binding site antibody 96%
- Modular DNA Barcoding of Nanobodies Enables Multiplexed in situ Protein Imaging and High-throughput Biomolecule Detection 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.