ImmunoDynamics Group, Programs in Computational Biology and Immunology, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Curr Opin Immunol. 2013 Feb;25(1):120-5. doi: 10.1016/j.coi.2012.12.001. Epub 2012 Dec 28.
T cells discriminate between peptide-MHC complexes on the surfaces of antigen presenting cells to enact appropriate downstream responses. Great progress has been made over the last 15 years in understanding varied aspects of T cell activation on short timescales (minutes), yet the mechanics and significance of long term T cell receptor signaling (hours or days) remain unclear. Furthermore, there remain some controversies regarding the correlation of the biophysical parameters of ligand-receptor interactions with the scaling of downstream effector functions. Here we review recent studies that emphasize the importance of long-term engagement of antigens to fine-tuning the activation of T cells over the duration of the complete immune response. We discuss how T cells dynamically regulate T cell receptor signaling via antigen crosstalk, competition and consumption to accurately counter antigenic challenges.
T 细胞能够区分抗原呈递细胞表面的肽-MHC 复合物,从而引发适当的下游反应。在过去的 15 年中,人们在理解 T 细胞在短时间(分钟)内的激活的各个方面取得了巨大进展,但 T 细胞受体信号转导的机制和意义(数小时或数天)仍不清楚。此外,关于配体-受体相互作用的生物物理参数与下游效应功能的扩展之间的相关性仍存在一些争议。在这里,我们回顾了最近的研究,这些研究强调了抗原的长期结合对于在整个免疫反应过程中精细调节 T 细胞的激活的重要性。我们讨论了 T 细胞如何通过抗原串扰、竞争和消耗来动态调节 T 细胞受体信号转导,从而准确地对抗抗原的挑战。