Auckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Wiley Interdiscip Rev Syst Biol Med. 2010 Jan-Feb;2(1):107-116. doi: 10.1002/wsbm.47.
Activation of T cells by antigen-presenting cells (APCs) in lymph nodes (LNs) is a key initiating event in many immune responses. Our understanding of this process has been both improved and complicated in recent years by evidence from techniques such as intravital microscopy that has revealed new levels of dynamism in the interaction of T cells and APCs. In particular, the complex motility of T cells within LNs, and their serial interactions with many APCs, imply that earlier static models of T cell activation need to be updated. Here we review the first attempts to model T cell interactions with APCs in LNs that incorporate simulations of T cell motility, based on experimental observations. We show that lattice-based modeling approaches are the dominant trend in these models, and then chart a possible course for development of these models toward spatially-resolved models of immune responses within LNs.
抗原呈递细胞 (APCs) 在淋巴结 (LNs) 中激活 T 细胞是许多免疫反应的关键起始事件。近年来,活体显微镜等技术提供的证据既改善了我们对这一过程的理解,也使其变得更加复杂,这些证据揭示了 T 细胞和 APC 相互作用的新动态水平。特别是,T 细胞在 LNs 中的复杂运动及其与许多 APC 的连续相互作用表明,需要更新 T 细胞激活的早期静态模型。在这里,我们回顾了基于实验观察,首次尝试将 T 细胞运动模拟纳入其中,以对 T 细胞与 LNs 中 APC 的相互作用进行建模的尝试。我们表明,基于格点的建模方法是这些模型中的主要趋势,然后为这些模型向 LNs 内免疫反应的空间分辨模型的发展绘制了一个可能的方向。