Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
Centro Hospitalar Lisboa Norte - Hospital de Santa Maria, Lisboa, Portugal.
Immunol Rev. 2019 Mar;288(1):112-127. doi: 10.1111/imr.12739.
Germinal centers (GC) have been known as key anatomic structures in humoral immunity, where isotype switching and affinity maturation occur. As a consequence, elucidation of GC regulation has potential implications for the understanding of autoantibody-mediated diseases. It is now accepted that different regulatory mechanisms coexist, including the action of a specialized population of Foxp3 regulatory T cells with unique access to the B-cell follicle: the T follicular regulatory (Tfr) cells. Tfr cells develop through a multistep process requiring migration through different compartments of lymphoid tissues. This review discusses the ontogeny and physiology of Tfr cells, their distribution within distinct anatomic compartments, and their function. A greater understanding of Tfr biology and GC regulation is likely to lead to better stratification of patients with autoantibody-mediated diseases, and to the identification of novel therapeutic targets.
生发中心(GC)一直是体液免疫的关键解剖结构,在此发生同种型转换和亲和力成熟。因此,阐明 GC 的调控机制可能有助于理解自身抗体介导的疾病。现在人们已经接受了不同的调控机制共存的观点,包括具有独特进入 B 细胞滤泡途径的 Foxp3 调节性 T 细胞(Treg)亚群的作用:滤泡调节性 T 细胞(Tfr)。Tfr 细胞通过需要通过淋巴组织不同区室迁移的多步骤过程发育。这篇综述讨论了 Tfr 细胞的发生和生理学、它们在不同解剖区室中的分布以及它们的功能。对 Tfr 生物学和 GC 调控的更深入了解可能会导致更好地对自身抗体介导的疾病患者进行分层,并确定新的治疗靶点。