Hamilton B L, Hamilton M S
Department of Biological Structure, University of Washington, Seattle 98195.
Am J Reprod Immunol Microbiol. 1987 Dec;15(4):153-5.
Female mice from four congenic strains were bred to males of the same four strains to determine the effect of maternal-fetal disparity at major histocompatibility complex (MHC) and the effect of non-MHC minor histocompatibility antigens on the weight of the feto-placental unit. An increase in feto-placental weights was found in all three of the four strains that could be evaluated when mother and fetus differed at multiple minor histocompatibility loci, irrespective of whether disparity at the MHC was present. No increase in feto-placental weights was found when mother and fetus differed at the MHC alone. The fact that these results were found in all strains studied suggests that the effect of maternal-fetal disparity at multiple minor histocompatibility antigens (minor HA) on the weight of the feto-placental unit is biologically significant. We conclude that if the increase in weight of the feto-placental unit results from immunostimulation, then minor histocompatibility antigens are the primary target of the maternal immune response to the histocompatibility antigens of the fetus.
将来自四个同类系的雌性小鼠与相同四个品系的雄性小鼠进行交配,以确定主要组织相容性复合体(MHC)处母胎差异以及非MHC次要组织相容性抗原对胎儿 - 胎盘单位重量的影响。当母亲和胎儿在多个次要组织相容性位点存在差异时,在四个可评估的品系中的三个品系中均发现胎儿 - 胎盘重量增加,而不论MHC处是否存在差异。当母亲和胎儿仅在MHC处存在差异时,未发现胎儿 - 胎盘重量增加。在所有研究的品系中均发现这些结果,这表明在多个次要组织相容性抗原(次要HA)处的母胎差异对胎儿 - 胎盘单位重量的影响具有生物学意义。我们得出结论,如果胎儿 - 胎盘单位重量的增加是由免疫刺激引起的,那么次要组织相容性抗原是母体对胎儿组织相容性抗原免疫反应的主要靶标。