Kunz H W, Gill T J
Transplantation. 1986 Aug;42(2):217-9. doi: 10.1097/00007890-198608000-00022.
The antibody response to the pregnancy-associated (Pa) antigen in the pregnant female segregated with the major histocompatibility complex (MHC) when the female progeny in the (PVG x WF)F1 x PVG testcross, in which the PVG strain is a low responder to Pa and the WF strain is a high responder, were mated to DA male rats. These results show that non-MHC immune response genes do not play a role, or at least any significant role, in the immune response to the paternal component of the placental antigens: the response approximates a unigenic trait with simple Mendelian segregation. Serological analysis showed that the antibodies formed by both the high responder (GMT 15, titer 1:32,768) and low responder (GMT 3, titer 1:8) female rats were directed against the Pa antigen. These findings show that the genetic control mechanism and the specificity of the antibody elicited by the placental antigen Pa are different from those in the responses to organ grafts and to soluble antigens.
在(PVG×WF)F1×PVG测交实验中,当雌性后代(其中PVG品系对妊娠相关(Pa)抗原反应较弱,WF品系反应较强)与DA雄性大鼠交配时,怀孕雌性对妊娠相关(Pa)抗原的抗体反应与主要组织相容性复合体(MHC)相关。这些结果表明,非MHC免疫反应基因在对胎盘抗原父系成分的免疫反应中不起作用,或者至少不起任何显著作用:这种反应类似于具有简单孟德尔分离的单基因性状。血清学分析表明,高反应性雌性大鼠(几何平均滴度15,效价1:32768)和低反应性雌性大鼠(几何平均滴度3,效价1:8)产生的抗体均针对Pa抗原。这些发现表明,胎盘抗原Pa引发的抗体的遗传控制机制和特异性不同于对器官移植和可溶性抗原的反应。