Buhl A M, Nemazee D, Cambier J C, Rickert R, Hertz M
Department of Pediatrics, National Jewish Medical and Research Center, Denver, Colorado, USA.
Immunol Rev. 2000 Aug;176:141-53. doi: 10.1034/j.1600-065x.2000.00613.x.
Experimental evidence contradicts the simplistic view that during development all B cells expressing non autoreactive antigen receptors on the cell surface are selected into the mature B-cell pool. While allelic exclusion, clonal selection and affinity maturation continue to define the mainstream notions of B-cell development and selection, new evidence is redefining our understanding of these processes. Receptor editing replaces functional B-cell receptors by secondary immunoglobulin gene rearrangements, a process that can play roles in both immune tolerance and immune response. In addition, editing can rescue cells that would otherwise fail positive selection. We focus here on our studies indicating that the functional competence of the B-cell antigen receptor complex plays a central role in the fate of developing B cells and their antigen receptor genes.
实验证据与一种简单化观点相矛盾,该观点认为在发育过程中,所有在细胞表面表达非自身反应性抗原受体的B细胞都会被选入成熟B细胞库。虽然等位基因排斥、克隆选择和亲和力成熟仍然是B细胞发育和选择的主流概念,但新证据正在重新定义我们对这些过程的理解。受体编辑通过二次免疫球蛋白基因重排取代功能性B细胞受体,这一过程在免疫耐受和免疫反应中都可能发挥作用。此外,编辑可以挽救那些否则将无法通过阳性选择的细胞。我们在此重点关注我们的研究,这些研究表明B细胞抗原受体复合物的功能能力在发育中的B细胞及其抗原受体基因的命运中起着核心作用。