Hertz M, Nemazee D
Division of Basic Sciences, National Jewish Medical and Research Center, Denver, Colorado 80206, USA.
Curr Opin Immunol. 1998 Apr;10(2):208-13. doi: 10.1016/s0952-7915(98)80250-1.
B cells that fail to pass a developmental checkpoint, either as immature or mature B cells, can be rescued by creating a new B cell antigen receptor through nested secondary immunoglobulin gene rearrangements, a process termed receptor editing. Tolerance-mediated receptor editing occurs in self-reactive immature bone marrow B cells, while peripheral receptor editing probably occurs in low-affinity B cells competing for antigen and for survival signals within the germinal center response.
未能通过发育检查点的B细胞,无论是未成熟的还是成熟的B细胞,都可以通过嵌套的二级免疫球蛋白基因重排来创建新的B细胞抗原受体而得到挽救,这一过程称为受体编辑。耐受性介导的受体编辑发生在自身反应性未成熟骨髓B细胞中,而外周受体编辑可能发生在生发中心反应中争夺抗原和生存信号的低亲和力B细胞中。