Coffey Francis, Alabyev Boris, Manser Tim
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Immunity. 2009 Apr 17;30(4):599-609. doi: 10.1016/j.immuni.2009.01.011. Epub 2009 Mar 19.
Current models of the germinal center (GC) response propose that after stimulation at the edges of T cell zones, pre-GC B cells directly migrate to the center of follicles and proliferate to form GCs. We followed the interrelationship of proliferation, differentiation, and microenvironmental locale in populations of pre-GC B cells responding to antigen. In contrast to the predictions of current models, after accumulation at the T-B interface, these cells appeared at the perimeter of follicles adjacent to the marginal zone. There, they rapidly proliferated for several days but underwent no V gene hypermutation and little heavy-chain class switching. Their chemokine receptor expression pattern indicated that these cells were sessile, yet they had begun to acquire many phenotypic characteristics of GC B cells. The expanded clones were subsequently observed in the center of follicles, suggesting that GCs are created by coalescence of B cells from this follicular perimeter response.
生发中心(GC)反应的当前模型提出,在T细胞区边缘受到刺激后,前生发中心B细胞直接迁移至滤泡中心并增殖形成生发中心。我们追踪了对抗原作出反应的前生发中心B细胞群体中增殖、分化和微环境定位之间的相互关系。与当前模型的预测相反,在T-B界面积累后,这些细胞出现在邻近距离边缘区的滤泡周边。在那里,它们迅速增殖数天,但未发生V基因超突变,并且几乎没有重链类别转换。它们的趋化因子受体表达模式表明这些细胞是固定的,但它们已开始获得许多生发中心B细胞的表型特征。随后在滤泡中心观察到扩增的克隆,这表明生发中心是由来自这种滤泡周边反应的B细胞合并形成的。