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Valkiers, S.

Publications and source records attributed to Valkiers, S..

7 recordsLinked to original sources

Deciphering antigen-driven T cell responses through vectorized TCRdist sequence neighborhood quantification

T cells provide precise mechanisms to defend the body against infection and malignancies, mediated through the expression of their hypervariable T cell receptors (TCRs). Interpreting similarity between TCRs, however, remains a significant challenge. While performant clustering methods exist, these often fail to distinguish between antigen-driven convergent selection and patterns arising stochastically from biases in the V(D)J recombination mechanism. Moreover, defining enrichment in sequence similarity among large repertoires is computationally taxing. To address these limitations, we present an efficient computational framework for rapid approximation of TCRdist distances using fixed-length vector embeddings and highly optimized nearest neighbor search, allowing sequence similarity enrichment testing at a multi-repertoire-wide scale. This framework leverages a novel shuffling-based background model that preserves important repertoire characteristics such as V gene frequency, CDR3 sequence length and generation probability more accurately than synthetic models. Together, these tools enable the efficient and robust identification of significantly neighbor enriched (SNE) TCR sequences at scale. We validate this approach by showing a significant enrichment of SNE clones in memory T cell fractions and further demonstrate its utility in identifying convergent T cell signatures of response to vaccination and viral infections, providing a scalable approach for antigen-agnostic T cell response profiling.

immunology↗

Diverse modes of T cell receptor sequence convergence define unique functional and cellular phenotypes

Single-cell techniques allow concurrent study of gene activity and T cell receptor (TCR) sequences, identifying connections between TCR structure and cell traits. Expanding on our CoNGA software, we present a "metaCoNGA" analysis of 6 million T cells from 91 diverse studies, mapping TCR sequence similarity across tissues and diseases. This approach exposes shared TCR features within specific T cell subsets, including those associated with infection, cancer, and autoimmunity. We introduce a method to identify T cell groups with similar gene expression and biased TCR amino acid composition, providing a systematic framework for classifying diverse unconventional T cells, including KIR+ CD8+ T cells, CD4+ regulatory T cells, and subsets of NKT and MAIT cells. A new TCR clustering approach identifies thousands of convergent TCR sequence clusters hypothesized to target shared antigens. These clusters show coherent gene expression, highlighting the role of antigen exposure in shaping T cell behavior. Finally, we provide a tool for users to merge new data with this resource and rapidly identify T cell features in their data sets. This resource empowers investigations into the complex relationship between TCR sequence and T cell function in human health.

immunology↗

Linking myelin and Epstein-Barr virus specific immune responses in multiple sclerosis: insights from integrated public T cell receptor repertoires

The autoimmune responses in multiple sclerosis (MS), particularly those mediated by T cells targeting CNS-derived antigens, are broadly recognized. However, the defining triggers underlying these responses remain poorly understood. Epstein-Barr virus (EBV) infection has emerged as a primary risk factor for MS, suggesting a potential role for molecular mimicry in which EBV-specific immune responses cross-react with myelin antigens. In this study, we analyzed the T cell receptor (TCR) repertoires of MS patients (n = 129) and controls (n = 94) from public datasets, to explore the relationship between EBV-specific and myelin-specific T cell responses. Our analysis identified clusters of TCRs that were significantly depleted among MS patients, many of which were associated with cytomegalovirus (CMV). By generating a library of myelin-reactive TCRs from stimulated peripheral blood mononuclear cells (PBMCs) obtained from MS patients and mapping these sequences to the public TCR repertoire database, we also uncovered a lower frequency of myelin-reactive TCRs in MS samples compared to controls in the public datasets. In addition, epitope-specificity prediction revealed a broader response to EBV-, but not CMV-derived epitopes. Collectively, these findings underscore the complex role of chronic viral infections in MS. Particularly, they suggest that EBV-specific immune responses contribute to the dysregulation of the immune system in MS patients, potentially through mechanisms of molecular mimicry. While the broader response to EBV-derived epitopes and the lower frequency of myelin-reactive TCRs in MS samples are both associated with the disease, further research is needed to clarify the nature of this relationship. These observations suggest that viral and autoimmune mechanisms may contribute independently or interact in MS pathogenesis.

immunology↗

Revealing the hidden sequence distribution of epitope-specific TCR repertoires and its influence on machine learning model performance

Numerous efforts have been made to decipher the epitope-T cell receptor (TCR) recognition code. Both simple machine learning techniques and deep learning strategies have been used to train models to predict the binding of epitopes by TCR sequences. A good training data set rests at the basis of every accurate prediction model, yet little attention has been given to the composition of these data sets. In this paper, we studied the natural distribution of TCR sequences within epitope-specific TCR repertoires, i.e. a set of TCRs binding the same epitope, and its impact on the predictability of TCR-epitope interactions. We found that the observed diversity of these repertoires can result from a smaller set of core binding motifs constrained by TCR generation. Moreover, a clear relationship was found between the sequence distribution of the training data and performance metrics, emphasizing the importance of the used ground-truth data when using machine learning models in this domain. Taken together, these findings inform data set composition to help push epitope-TCR prediction models to the next level.

bioinformatics↗

STEGO.R: an application to aid in scRNA-seq and scTCR-seq processing and analysis.

The T-cell receptor (TCR) carries critical information regarding T-cell functionality. The TCR, despite its importance, is underutilized in single cell transcriptomics, with gene expression (GEx) features solely driving current analysis strategies. Here, we argue for a switch to a TCR-first approach, which would uncover unprecedented insights into T cell and TCR repertoire mechanics. To this end, we curated a large T-cell atlas from 12 prominent human studies, containing in total 500,000 T cells spanning multiple diseases, including melanoma, head-and-neck cancer, T-cell cancer, and lung transplantation. Herein, we identified severe limitations in cell-type annotation using unsupervised approaches and propose a more robust standard using a semi-supervised method or the TCR arrangement. We then showcase the utility of a TCR-first approach through application of the novel STEGO.R tool for the successful identification of hyperexpanded clones to reveal treatment-specific changes. Additionally, a meta-analysis based on neighbor enrichment revealed previously unknown public T-cell clusters with potential antigen-specific properties as well as highlighting additional common TCR arrangements. Therefore, this paradigm shift to a TCR-first with STEGO.R highlights T-cell features often overlooked by conventional GEx-focused methods, and enabled identification of T cell features that have the potential for improvements in immunotherapy and diagnostics. One Sentence SummaryRevamping the interrogation strategies for single-cell data to be centered on T cell receptor (TCR) rather than the generic gene expression improved the capacity to find relevant disease specific TCR. Key PointsO_LIThe TCR-first approach captures dynamic T cell features, even within a clonal population. C_LIO_LIA novel [~]500,000 T-cell atlas to enhance single cell analysis, especially for restricted populations. C_LIO_LINovel STEGO.R program and pipeline allows for consistent and reproducible interrogating of scTCR-seq with GEx. C_LI

bioinformatics↗

RapTCR: Rapid exploration and visualization of T-cell receptor repertoires

AO_SCPLOWBSTRACTC_SCPLOWO_ST_ABSMotivationC_ST_ABSThe acquisition of T-cell receptor (TCR) repertoire sequence data has become faster and cheaper due to advancements in high-throughput sequencing. However, fully exploiting the diagnostic and clinical potential within these TCR repertoires requires a thorough understanding of the inherent repertoire structure. Hence, visualizing the full space of TCR sequences could be a key step towards enabling exploratory analysis of TCR repertoire, driving their enhanced interrogation. Nonetheless, current methods remain limited to rough profiling of TCR V and J gene distributions. Addressing this need, we developed RapTCR, a tool for rapid visualization and post-analysis of TCR repertoires. ApproachTo overcome computational complexity, RapTCR introduces a novel, simple embedding strategy that represents TCR amino acid sequences as short vectors while retaining their pairwise alignment similarity. RapTCR then applies efficient algorithms for indexing these vectors and constructing their nearest neighbor network. It provides multiple visualization options to map and interactively explore a TCR network as a two-dimensional representation. Benchmarking analyses using epitope-annotated datasets demonstrate that these RapTCR visualizations capture TCR similarity features on a global level (e.g., J gene) and locally (e.g., epitope reactivity). RapTCR is available as a Python package, implementing the intuitive scikit-learn syntax to easily generate insightful, publication-ready figures for TCR repertoires of any size. Availability and ImplementationRapTCR was written in Python 3. It is available as an anaconda package (https://anaconda.org/vincentvandeuren/raptcr), and on github (https://github.com/vincentvandeuren/RapTCR). Documentation and example notebooks are available at vincentvandeuren.github.io/rapTCR_docs/. Contactpieter.meysman@uantwerpen.be

bioinformatics↗

clusTCR: a Python interface for rapid clustering of large sets of CDR3 sequences

The T-cell receptor (TCR) determines the specificity of a T-cell towards an epitope. As of yet, the rules for antigen recognition remain largely undetermined. Current methods for grouping TCRs according to their epitope specificity remain limited in performance and scalability. Multiple methodologies have been developed, but all of them fail to efficiently cluster large data sets exceeding 1 million sequences. To account for this limitation, we developed clusTCR, a rapid TCR clustering alternative that efficiently scales up to millions of CDR3 amino acid sequences. Benchmarking comparisons revealed similar accuracy of clusTCR with other TCR clustering methods. clusTCR offers a drastic improvement in clustering speed, which allows clustering of millions of TCR sequences in just a few minutes through efficient similarity searching and sequence hashing. clusTCR was written in Python 3. It is available as an anaconda package (https://anaconda.org/svalkiers/clustcr) and on github (https://github.com/svalkiers/clusTCR).

bioinformatics↗