Bosma M J, Bosma G C, Owen J L
Eur J Immunol. 1978 Aug;8(8):562-8. doi: 10.1002/eji.1830080805.
Adoptive lymphocyte transfers between Iga, Igb and Igd allotype-congenic mouse strains revealed host barriers against the production of certain donor allotypes. First, as recipients of Igb cells, Iga and Igd mice permitted the production of donor Ig-4b but not that of Ig-1 b. The apparent mediators of this Ig-1 b barrier were T cells specific for Ig- 1 b determinants on B cells. Additional cell transfers showed Iga mice to have a second barrier against allotype production by Igd donor cells. Reciprocal cell transfers showed Igb and Igd mice to have comparatively weak barriers against Iga-producing cells. As host barriers were absent in mice deficient for T cells (athymic nude mice), it appears that they are T cell-mediated. Further, the allotype-dependence of such barriers means that the antigens responsible must be under the control of allotype-linked genes. The regulatory implications of this for the immune system are discussed.
在Iga、Igb和Igd同种异型基因纯合小鼠品系之间进行的过继性淋巴细胞转移揭示了宿主对某些供体同种异型产生的屏障作用。首先,作为Igb细胞的受体,Iga和Igd小鼠允许产生供体Ig-4b,但不允许产生Ig-1b。这种Ig-1b屏障的明显介导者是对B细胞上Ig-1b决定簇具有特异性的T细胞。进一步的细胞转移表明,Iga小鼠对Igd供体细胞产生同种异型具有第二种屏障。相互的细胞转移表明,Igb和Igd小鼠对产生Iga的细胞具有相对较弱的屏障。由于在缺乏T细胞的小鼠(无胸腺裸鼠)中不存在宿主屏障,所以似乎它们是由T细胞介导的。此外,这种屏障的同种异型依赖性意味着负责的抗原必须受同种异型连锁基因的控制。本文讨论了这对免疫系统的调节意义。