Kennedy Institute of Rheumatology, Nuffield Department of Orthopedics, Rheumatology, and Musculoskeletal Sciences, The University of Oxford, Roosevelt Drive, Headington OX3 7FY, UK; Skirball Institute of Biomolecular Medicine, Department of Pathology, New York University School of Medicine, 540 First Avenue, New York, NY 10016, USA.
Mol Cell. 2014 Apr 24;54(2):255-62. doi: 10.1016/j.molcel.2014.04.001.
Molecular interactions at the interface between helper T cells and antigen-presenting B cells govern the ability to produce specific antibodies, which is a central event in protective immunity generated by natural infection or man-made vaccines. In order for a T cell to deliver effective help to a B cell and guide affinity maturation, it needs to provide feedback that is proportional to the amount of antigen the B cell collects with its surface antibody. This review focuses on mechanisms by which T and B cells manage to count the products of antigen capture and encourage B cells with the best receptors to dominate the response and make antibody-producing plasma cells. We discuss what is known about the proportionality of T cells responses to presented antigens and consider the mechanisms that B cells may use to keep count of positive feedback from T cells.
辅助性 T 细胞和抗原呈递 B 细胞之间界面的分子相互作用决定了产生特异性抗体的能力,这是自然感染或人工疫苗产生保护性免疫的核心事件。为了使 T 细胞向 B 细胞提供有效的帮助并指导亲和力成熟,它需要提供与 B 细胞通过其表面抗体收集的抗原量成比例的反馈。这篇综述重点介绍了 T 细胞和 B 细胞如何设法计算抗原捕获产物并鼓励具有最佳受体的 B 细胞主导反应并产生产生抗体的浆细胞的机制。我们讨论了已知的 T 细胞对呈递抗原的反应的比例性,并考虑了 B 细胞可能用于计算来自 T 细胞的正反馈的机制。