Area of Immunology, Faculty of Biology, Biomedical Research Center (CINBIO), Universidade de Vigo, 36310 Vigo, Spain.
Instituto Gulbenkian de Ciência, 2781-901 Oeiras, Portugal.
Cells. 2021 Apr 28;10(5):1040. doi: 10.3390/cells10051040.
Our current quantitative knowledge of the kinetics of antibody-mediated immunity is partly based on idealized experiments throughout the last decades. However, new experimental techniques often render contradictory quantitative outcomes that shake previously uncontroversial assumptions. This has been the case in the field of T-cell receptors, where recent techniques for measuring the 2-dimensional rate constants of T-cell receptor-ligand interactions exposed results contradictory to those obtained with techniques measuring 3-dimensional interactions. Recently, we have developed a mathematical framework to rationalize those discrepancies, focusing on the proper fine-grained description of the underlying kinetic steps involved in the immune synapse. In this perspective article, we apply this approach to unveil potential blind spots in the case of B-cell receptors (BCR) and to rethink the interactions between B cells and follicular dendritic cells (FDC) during the germinal center (GC) reaction. Also, we elaborate on the concept of "catch bonds" and on the recent observations that B-cell synapses retract and pull antigen generating a "retracting force", and propose some testable predictions that can lead to future research.
我们目前对抗体介导免疫动力学的定量知识部分基于过去几十年的理想化实验。然而,新的实验技术经常会产生相互矛盾的定量结果,动摇以前无争议的假设。这在 T 细胞受体领域就是如此,最近用于测量 T 细胞受体-配体相互作用的二维速率常数的技术得出的结果与那些测量三维相互作用的技术得出的结果相矛盾。最近,我们开发了一个数学框架来使这些差异合理化,重点是对免疫突触中涉及的基本动力学步骤进行适当的细粒度描述。在这篇观点文章中,我们应用该方法揭示 B 细胞受体 (BCR) 情况下的潜在盲点,并重新思考生发中心 (GC) 反应期间 B 细胞与滤泡树突状细胞 (FDC) 之间的相互作用。此外,我们详细阐述了“捕获键”的概念,以及最近观察到的 B 细胞突触回缩并拉动产生“回缩力”的抗原的现象,并提出了一些可进行测试的预测,这些预测可能会带来未来的研究。