Iwata I, Shimizu S, Yamaguchi N
Am J Reprod Immunol Microbiol. 1986 Jun;11(2):55-8. doi: 10.1111/j.1600-0897.1986.tb00029.x.
The active immune responsiveness of the offspring of pregnant mice stimulated with heterologous protein antigen was investigated by measuring the plaque-forming cells (PFC). Mice (C57BL/10;B10) immunized once in pregnancy with ovalbumin (OVA) in the form of Al(OH)3 gel (in alum) or in a soluble form (in saline) developed no anti-OVA PFC response. The anti-OVA PFC response suppression induced in the offspring was high in the offspring of alum-treated mothers and low in those of saline-treated mothers. The optimal dose of OVA in alum that induces the highest immunological memory in pregnant mice caused the complete suppression of PFC development in their offspring. The same dose of OVA in saline induced a negative immunological memory in pregnant mice and partial suppression in the offspring. On the other hand, mice primed prior to conception and boosted during pregnancy developed anti-OVA PFC in significant numbers, and only a partial suppression was established in their young. Based on these data, we discussed the possible mechanisms concerned with the specific suppression induced in the young B10 mice stimulated by OVA.
通过测量空斑形成细胞(PFC),研究了用异源蛋白抗原刺激的怀孕小鼠后代的主动免疫反应性。在怀孕期间用氢氧化铝凝胶(明矾中)或可溶性形式(盐水中)的卵清蛋白(OVA)免疫一次的小鼠(C57BL/10;B10)未产生抗OVA PFC反应。在明矾处理的母亲的后代中,后代中诱导的抗OVA PFC反应抑制程度高,而在盐水处理的母亲的后代中则低。在怀孕小鼠中诱导最高免疫记忆的明矾中OVA的最佳剂量导致其后代中PFC发育完全受到抑制。盐水中相同剂量的OVA在怀孕小鼠中诱导了负免疫记忆,并在后代中产生了部分抑制。另一方面,在受孕前致敏并在怀孕期间加强免疫的小鼠产生了大量的抗OVA PFC,并且在它们的幼崽中仅建立了部分抑制。基于这些数据,我们讨论了与OVA刺激的年轻B10小鼠中诱导的特异性抑制有关的可能机制。