Hollmann C, Gerdes J
J Pathol. 1999 Oct;189(2):147-9. doi: 10.1002/(SICI)1096-9896(199910)189:2<147::AID-PATH433>3.0.CO;2-8.
The humoral immune response constitutes an efficient system to protect the organism against diseases caused by invading pathogens. To guarantee a highly efficient defence, the humoral immune system has to be tightly regulated. Two cell subsets in particular, T cells and follicular dendritic cells (FDCs), contribute to the success of these regulation processes. Whereas the particular role of T cells is the elimination of autoreactive clones, the main role of FDCs is to present unprocessed antigen and check B-cell clones for higher affinity. B-cell clones unsuited for improved humoral immune response will be specifically killed. Involvement of Fas-mediated apoptosis might be an additional tool not only in T-cell-mediated regulation, but also in FDC-B cell interaction in the germinal centre.
体液免疫反应构成了一个有效的系统,以保护机体抵御由入侵病原体引起的疾病。为确保高效防御,体液免疫系统必须受到严格调控。特别是两种细胞亚群,即T细胞和滤泡树突状细胞(FDC),对这些调控过程的成功发挥作用。T细胞的特定作用是消除自身反应性克隆,而FDC的主要作用是呈递未加工的抗原,并检查B细胞克隆是否具有更高的亲和力。不适合改善体液免疫反应的B细胞克隆将被特异性杀伤。Fas介导的细胞凋亡的参与可能不仅是T细胞介导的调控中的一种额外手段,也是生发中心FDC与B细胞相互作用中的一种额外手段。