Gray George I, Chukwuma P Chukwunalu, Eldaly Bassant, Perera W W J Gihan, Brambley Chad A, Rosales Tatiana J, Baker Brian M
Department of Chemistry and Biochemistry and the Harper Cancer Research Institute, University of Notre Dame, Notre Dame, Indiana, USA.
Immunol Rev. 2025 Jan;329(1):e13439. doi: 10.1111/imr.13439.
αβ T cell receptor (TCR) recognition of peptide-MHC complexes lies at the core of adaptive immunity, balancing specificity and cross-reactivity to facilitate effective antigen discrimination. Early structural studies established basic frameworks helpful for understanding and contextualizing TCR recognition and features such as peptide specificity and MHC restriction. However, the growing TCR structural database and studies launched from structural work continue to reveal exceptions to common assumptions and simplifications derived from earlier work. Here we explore our evolving understanding of TCR recognition, illustrating how structural and biophysical investigations regularly uncover complex phenomena that push against paradigms and expand our understanding of how TCRs bind to and discriminate between peptide/MHC complexes. We discuss the implications of these findings for basic, translational, and predictive immunology, including the challenges in accounting for the inherent adaptability, flexibility, and occasional biophysical sloppiness that characterize TCR recognition.
αβ T细胞受体(TCR)对肽 - 主要组织相容性复合体(MHC)的识别是适应性免疫的核心,它平衡特异性和交叉反应性以促进有效的抗原识别。早期的结构研究建立了有助于理解和定位TCR识别以及诸如肽特异性和MHC限制等特征的基本框架。然而,不断增长的TCR结构数据库以及基于结构研究开展的各项研究持续揭示出与早期工作中常见假设和简化情况相悖的例外情况。在这里,我们探讨我们对TCR识别不断演变的理解,阐述结构和生物物理研究如何经常揭示出复杂现象,这些现象突破了范式并拓展了我们对TCR如何结合并区分肽/MHC复合体的理解。我们讨论了这些发现对基础、转化和预测性免疫学的影响,包括在解释TCR识别所具有的内在适应性、灵活性以及偶尔出现的生物物理不精确性方面所面临的挑战。