Goodman J W, Bosma G C
Immunology. 1967 Aug;13(2):125-40.
Attempts were made to immunize F hybrid mice to their inbred parental strains by active immunization with either living or dead parental cells and by adoptive transfer of isogenic (F) lymph node cells to irradiated hybrids that subsequently received parental bone marrow. Cumulative mortality studies and erythrocyte serotyping revealed that many mice survived and retained their parental grafts for long periods of time. In most experiments reported here, Fe uptake by erythrocytes and spleens of chimeras 1 week after marrow transplantation was used as a measure of erythropoiesis and thereby of success or failure of the marrow graft. Pre-treatment (`pre-immunization') of hybrids with parental spleen cells produced no evidence of specific immunization. However, pre-treatment with spleen cells from parent 1 was detrimental to subsequently transplanted marrow from parent 2 and vice-versa. Adoptive transfer of viable F lymph node cells failed to decrease growth of parental cells in irradiated F hybrids. These findings indicate that the poor-growth phenomenon of particular parent—F combinations cannot be explained in terms of classical immune rejection of parental cells by F hybrids. Instead, growth of parental cells in the F environment is inhibited or delayed.
尝试通过用活的或死的亲本细胞进行主动免疫,以及将同基因(F)淋巴结细胞过继转移到经照射的杂种小鼠体内(随后这些杂种小鼠接受亲本骨髓),使F杂种小鼠对其近交亲本品系产生免疫。累积死亡率研究和红细胞血清分型显示,许多小鼠存活下来并长时间保留了其亲本移植物。在本文报道的大多数实验中,骨髓移植1周后嵌合体红细胞和脾脏对铁的摄取被用作衡量红细胞生成的指标,从而衡量骨髓移植的成败。用亲本脾细胞对杂种小鼠进行预处理(“预免疫”)未产生特异性免疫的证据。然而,用亲本1的脾细胞进行预处理对随后移植的亲本2的骨髓有害,反之亦然。将活的F淋巴结细胞过继转移未能降低经照射的F杂种小鼠中亲本细胞的生长。这些发现表明,特定亲本 - F组合的生长不良现象不能用F杂种小鼠对亲本细胞的经典免疫排斥来解释。相反,亲本细胞在F环境中的生长受到抑制或延迟。