Perlmutter R M, Kearney J F, Chang S P, Hood L E
Science. 1985 Mar 29;227(4694):1597-601. doi: 10.1126/science.3975629.
Although antibody diversity arises mainly from apparently random combinatorial and somatic mutational mechanisms acting upon a limited number of germline antibody genes, the antibody repertoire develops in an ordered fashion during mammalian ontogeny. A series of early pre-B and B-lymphocyte cell lines were examined to determine whether an ordered rearrangement of gene families of the variable region of immunoglobulin heavy chains (VH) may be the basis for the programmed development of the antibody response. The results indicated that the VH repertoire of fetal B-lineage cells is largely restricted to the VH 7183 gene family and that subsequent recruitment of additional VH gene families occurs during neonatal development. These results have important implications in understanding the ontogeny of immune function.
尽管抗体多样性主要源于作用于有限数量种系抗体基因的明显随机的组合和体细胞突变机制,但抗体库在哺乳动物个体发育过程中以有序方式发展。研究了一系列早期前B淋巴细胞和B淋巴细胞系,以确定免疫球蛋白重链(VH)可变区基因家族的有序重排是否可能是抗体反应程序性发展的基础。结果表明,胎儿B系细胞的VH库在很大程度上局限于VH 7183基因家族,并且在新生儿发育过程中会发生额外VH基因家族的后续募集。这些结果对于理解免疫功能的个体发育具有重要意义。