Learning the principles of T cell antigen discernment

Abstract

T cells are central to the adaptive immune response, capable of detecting pathogenic antigens while ignoring healthy tissues with remarkable specificity and sensitivity. Quantitatively understanding how T cell receptors (TCRs) discriminate among antigens requires biophysical models and theoretical analysis of signaling networks. Here, we review current theoretical frameworks of antigen recognition in the context of modern experimental and computational advances. Antigen potency spans a continuum and exhibits nonlinear effects within complex mixtures, challenging discrete classification and simple threshold-based models. This complexity motivates the development of models such as adaptive kinetic proofreading, which integrate both activating and inhibitory signals. Advances in high-throughput technologies now generate large-scale, quantitative datasets, enabling the refinement of such models through statistical and machine learning approaches. This convergence of theory, data, and computation promises deeper insights into immune decision-making and opens new avenues for rational immunotherapy design.