Decoding Human T Cell Immunity with Artificial Intelligence and Single-Cell Genomics
T cells are key mediators of adaptive immunity, yet their highly dynamic response states and immense T cell receptor (TCR) diversity pose challenges in deciphering their functional roles in human diseases. Recent advances in single-cell genomics and TCR sequencing provide unprecedented opportunities to resolve T cell heterogeneity, decode clonal response dynamics, and facilitate high-throughput antigen specificity mapping. In this review, we summarize major technological innovations that have transformed T cell research, from experimental tools for antigen-specific T cell profiling to machine learning frameworks for predicting interactions between the TCR and peptide-MHC (pMHC) and structural modeling powered by deep learning. We discuss current bottlenecks, including data limitations and model generalizability, and explore emerging strategies to guide the next generation of T cell discoveries. We argue that artificial intelligence and single-cell genomics will collectively pave the way for dissecting T cell heterogeneity, mapping TCR sequence to pMHC specificity, and interpreting these features in the context of clinical outcomes.
Authors
- Lisa M. Dratva (ORCID: https://orcid.org/0000-0002-2873-6787)
- Lorenz Kretschmer (ORCID: https://orcid.org/0000-0003-0987-8429)
- Sarah A. Teichmann
Institutions
- Canadian Institute for Advanced Research (CA)
- University of Cambridge (GB)
- Cambridge School (PT)
- Bridge University (SS)
- Stem Cell Institute (PA)
Publication Details
- Journal
- Annual Review of Immunology
- Published
- 2026-04-27
- DOI
- https://doi.org/10.1146/annurev-immunol-082724-011631
- Primary Topic
- vaccines and immunoinformatics approaches
- Type
- article
- Field-Weighted Citation Impact
- 0.00